Milk in the Northeast and Other Marketing Areas; Final Decision on Proposed Amendments to Marketing Agreements and Orders, 33534-33553 [2010-12771]
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33534
Proposed Rules
Federal Register
Vol. 75, No. 113
Monday, June 14, 2010
This section of the FEDERAL REGISTER
contains notices to the public of the proposed
issuance of rules and regulations. The
purpose of these notices is to give interested
persons an opportunity to participate in the
rule making prior to the adoption of the final
rules.
DEPARTMENT OF AGRICULTURE
Agricultural Marketing Service
7 CFR Part 1000
[Doc. No. AMS–DA–09–0062; AO–14–A73, et
al.; DA–03–10]
Milk in the Northeast and Other
Marketing Areas; Final Decision on
Proposed Amendments to Marketing
Agreements and Orders
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AGENCY: Agricultural Marketing Service,
USDA.
ACTION: Proposed rule.
SUMMARY: This final decision maintains
the current fluid milk product
definition’s compositional standard of
6.5 percent nonfat milk solids criterion
and incorporates an equivalent 2.25
percent true milk protein criterion for
determining if a product meets the
compositional standard. The decision
also determines how milk and milkderived ingredients should be priced
under all Federal milk marketing orders
when used in products meeting the
fluid milk product definition. The
decision provides exemptions for
drinkable yogurt products containing at
least 20 percent yogurt (by weight),
kefir, and products intended to be meal
replacements from the fluid milk
product definition. The orders as
amended are subject to producer
approval by referendum before they can
be implemented.
FOR FURTHER INFORMATION CONTACT:
Henry H. Schaefer, Economist, USDA/
AMS/Dairy Programs, Upper Midwest
Milk Market Administrators Office,
Suite 200, 1600 West 82nd Street,
Minneapolis, Minnesota 55431–1420,
(952) 831–5292, e-mail address:
hschaefer@fmma30.com; or William
Francis, Associate Deputy
Administrator, USDA/AMS/Dairy
Programs, Order Formulation and
Enforcement, Stop 0231–Room 2971–S,
1400 Independence Avenue, SW.,
Washington, DC 20250–0231, (202) 720–
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6274, e-mail address:
william.francis@ams.usda.gov.
SUPPLEMENTARY INFORMATION: This final
decision maintains the current fluid
milk product definition’s compositional
standard of 6.5 percent nonfat milk
solids and incorporates an equivalent
2.25 percent true milk protein criterion
for determining if a product meets the
compositional standard. The decision
also determines how milk and milkderived ingredients should be priced
under all Federal milk marketing orders
when used in products meeting the
fluid milk product definition. The
decision exempts drinkable yogurt
products containing at least 20 percent
yogurt (by weight), kefir, infant
formulas, dietary products (meal
replacements) and other products that
may contain milk-derived ingredients
from the fluid milk product definition.
This administrative action is governed
by the provisions of Sections 556 and
557 of Title 5 of the United States Code
and, therefore, is excluded from the
requirements of Executive Order 12866.
The proposed amendments to the rules
herein have been reviewed under
Executive Order 12988, Civil Justice
Reform. They are not intended to have
a retroactive effect. The Agricultural
Marketing Agreement Act of 1937 (Act),
as amended (7 U.S.C. 604–674),
provides that administrative
proceedings must be exhausted before
parties may file suit in court. Under
Section 608c(15)(A) of the Act, any
handler subject to an order may request
modification or exemption from such
order by filing with the Department a
petition stating that the order, any
provision of the order, or any obligation
imposed in connection with the order is
not in accordance with the law. A
handler is afforded the opportunity for
a hearing on the petition. After a
hearing, the Department would rule on
the petition. The Act provides that the
district court of the United States in any
district in which the handler is a
habitant, or has its principal place of
business, has jurisdiction in equity to
review the USDA’s ruling on the
petition, provided a bill in equity is
filed not later than 20 days after the date
of the entry of the ruling.
Regulatory Flexibility Act and
Paperwork Reduction Act
In accordance with the Regulatory
Flexibility Act (5 U.S.C. 601 et seq.), the
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Agricultural Marketing Service has
considered the economic impact of this
action on small entities and has certified
that this proposed rule will not have a
significant economic impact on a
substantial number of small entities. For
the purpose of the Regulatory Flexibility
Act, a dairy farm is considered a ‘‘small
business’’ if it has an annual gross
revenue of less than $750,000, and a
dairy products manufacturer is a ‘‘small
business’’ if it has fewer than 500
employees.
For the purposes of determining
which dairy farms are ‘‘small
businesses,’’ the $750,000 per year
criterion was used to establish a
production guideline of 500,000 pounds
per month. Although this guideline does
not factor in additional monies that may
be received by dairy producers, it
should be an inclusive standard for
most ‘‘small’’ dairy farmers. For
purposes of determining a handler’s
size, if the plant is part of a larger
company operating multiple plants that
collectively exceed the 500-employee
limit, the plant will be considered a
large business even if the local plant has
fewer than 500 employees.
For the month of June 2005, the
month the hearing was held, 52,425
dairy farmers were pooled on the
Federal order system. Of the total,
49,160, or 94 percent were considered
small businesses. During the same
month, 1,530 plants were regulated by
or reported their milk receipts to their
respective Market Administrator. Of the
total, 847, or 55 percent were
considered small businesses.
The fluid milk product definition sets
out the criteria for determining if the
use of producer milk and milk-derived
ingredients in such products should be
priced at the Class I price. The
established criteria for the classification
of producer milk are applied in an
identical fashion to both large and small
businesses and will not have any
different impact on those businesses
producing fluid milk products thus
assuring that similarly situated handlers
have the same minimum price as
required by Section 608(c)5 of the Act.
Therefore, the amendments will not
have a significant economic impact on
a substantial number of small entities.
The impact of the proposed
amendments on large and small entities
would be negligible. In fact, the
amendment proposing to change the
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classification of kefir and drinkable
yogurt is estimated to affect blend prices
by no more than $ 0.0026 per cwt based
on record evidence.
The Agricultural Marketing Service is
committed to complying with the EGovernment Act to promote the use of
the Internet and other information
technologies to provide increased
opportunities for citizen access to
Government information and services,
and for other purposes.
A review of reporting requirements
was completed under the Paperwork
Reduction Act of 1995 (44 U.S.C.
Chapter 35). It was determined that
these amendments would have no
impact on reporting, recordkeeping, or
other compliance requirements because
they would remain identical to the
current requirements. No new forms are
proposed and no additional reporting
requirements are necessary.
This notice does not require
additional information collection that
needs clearance by the Office of
Management and Budget (OMB) beyond
currently approved information
collection. The primary sources of data
used to complete the forms are routinely
used in most business transactions. The
forms require only a minimal amount of
information that can be supplied
without data processing equipment or a
trained statistical staff. Thus, the
information collection and reporting
burden is relatively small. Requiring the
same reports for all handlers does not
significantly disadvantage any handler
that is smaller than the industry
average.
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Prior Documents in This Proceeding
Notice of Hearing: Issued April 6,
2005; published April 12, 2005 (70 FR
19012).
Recommended Decision: Issued May
12, 2006; published May 17, 2006 (71
FR 28590).
Preliminary Statement
Notice is hereby given of the filing
with the Hearing Clerk of this final
decision with respect to the proposed
amendments to the marketing
agreements and the orders regulating the
handling of milk in the Northeast and
other marketing areas. This notice is
issued pursuant to the provisions of the
Agricultural Marketing Agreement Act
and applicable rules of practice and
procedure governing the formulation of
marketing agreements and marketing
orders (7 CFR Part 900).
A public hearing was held upon
proposed amendments to the marketing
agreements and the orders regulating the
handling of milk in all Federal milk
marketing areas. The hearing was held
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pursuant to the provisions of the
Agricultural Marketing Agreement Act
of 1937 (AMAA), as amended (7 U.S.C.
601–674), and the applicable rules of
practice and procedure governing the
formulation of marketing agreements
and marketing orders (7 CFR Part 900).
The proposed amendments set forth
below are based on the record of a
public hearing held in Pittsburgh,
Pennsylvania, on June 20–23, 2005,
pursuant to a notice of hearing issued
April 6, 2005 and published April 12,
2005 (70 FR 19012); and a
recommended decision issued May 12,
2006 and published May 17, 2006 (71
FR 28590).
The material issues on the record of
the hearing relate to:
1. Amending the fluid milk product
definition.
Findings and Conclusions
This final decision maintains the
current fluid milk product definition’s
compositional standard of 6.5 percent
nonfat milk solids and incorporates an
equivalent 2.25 percent true milk
protein criterion for determining
whether a product meets the
compositional standard. The decision
also determines how milk and milkderived ingredients should be priced
under all orders when used in products
meeting the fluid milk product
definition. The decision exempts
drinkable yogurt products containing at
least 20 percent yogurt (by weight),
kefir, infant formulas, dietary products
(meal replacements) and other products
that may contain milk-derived
ingredients from the fluid milk product
definition.
All Federal milk orders currently state
that ‘‘fluid milk product means any milk
products in fluid or frozen form
containing less than 9 percent butterfat
that are intended to be used as
beverages.’’ The fluid milk product
definition also contains a non-definitive
list of dairy products that are named
fluid milk products. In addition to the
compositional butterfat standard fluid
milk products shall not include, among
other products, ‘‘* * * any product that
contains by weight less than 6.5 percent
nonfat milk solids * * *’’ Dairy
products that do not fall within these
limits are not considered fluid milk
products and the milk used to produce
these products is classified in Class II,
Class III or Class IV, depending on the
form or purpose for which the products
are to be used.
Eleven proposals were published in
the hearing notice for this proceeding.
Proposals 1, 3, 4 and 6 were abandoned
at the hearing by their proponents in
support of other noticed proposals. No
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further reference to these proposals will
be made.
A proposal published in the hearing
notice as Proposal 2, offered by Dairy
Farmers of America, Inc. (DFA), seeks to
amend the fluid milk product definition
to include any dairy ingredient,
including whey, when calculating the
milk contained in a product on a
protein-equivalent or nonfat solids
equivalent basis. DFA is a dairy farmermember owned cooperative and at the
time of the hearing had 12,800 member
farms located in 49 states whose
members’ milk is pooled throughout the
Federal order system.
H.P. Hood LLC (H.P. Hood) owns and
operates milk processing and
manufacturing plants in the Eastern and
Midwest United States and is the
proponent of a proposal published in
the hearing notice as Proposal 5 that
was modified at the hearing. As
modified, Proposal 5 seeks to amend the
fluid milk product definition to include
any product that, based upon
substantial evidence as determined by
the Department, directly competes with
other fluid milk products and that the
Department must make a written
determination before any product can be
classified as a fluid milk product.
A proposal published in the hearing
notice as Proposal 7 was offered by the
National Milk Producers Federation
(NMPF). At the time of the hearing
NMPF consisted of 33 dairy-farmer
member cooperatives that represented
more than 75 percent of U.S. dairy
farmers. Proposal 7 seeks to amend the
fluid milk product definition by
removing the reference ‘‘6.5 percent
nonfat solids standard and whey,’’ and
adopting a 2.25 percent true milk
protein criterion. During the hearing,
DFA offered a modification to Proposal
7 by seeking to authorize the
Department to make an interim
classification determination for new
products that result from new
technology. The Department would then
convene a hearing to address the use of
the new technology in classification
decisions and make a final classification
determination for the new product
within one year.
Proposal 8 seeks to amend the fluid
milk product definition by excluding
yogurt-containing beverages from the
fluid milk product definition. This
proposal was offered by The Dannon
Company, Inc. (Dannon), a wholly
owned subsidiary of The Danone Group
that produces yogurt and fresh dairy
products in 40 countries, including the
United States.
Proposal 9 also seeks to amend the
fluid milk product definition by
excluding drinkable food products with
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no more than 2.2 percent skim milk
protein provided the product contains at
least 20 percent yogurt (nonfat yogurt,
lowfat yogurt or yogurt) by weight from
the fluid milk product definition.
Proposal 9 was offered by General Mills,
Inc. (General Mills), a food
manufacturer that markets such
products as Yoplait yogurt and yogurtcontaining products in over 100
countries, including the United States.
A proposal published in the hearing
notice as Proposal 10 was offered by the
Novartis Nutrition Corporation
(Novartis). Novartis develops and
manufactures a variety of products,
including milk-based products,
designed to meet specific nutritional
needs. Proposal 10 seeks to amend the
fluid milk product definition by
excluding formulas prepared for dietary
use by removing the words ‘‘(meal
replacement) that are packaged in
hermetically-sealed containers.’’ The
proposal would remove the 6.5 percent
nonfat milk solids standard.
A proposal published in the hearing
notice as Proposal 11 seeks to amend
the fluid milk product definition by
excluding health care beverages
distributed to the health care industry.
Proposal 11 was offered by Hormel
Foods, LLC (Hormel), a wholly owned
subsidiary of Hormel Foods Corporation
and manufacturer of a variety of food
products primarily for the health care
industry.
A witness appearing on behalf of
NMPF testified in support of Proposal 7.
The witness testified that Proposal 7
would close loopholes in the current
fluid milk product definition that have
allowed products developed as a result
of new technology to avoid
classification as fluid milk products.
The witness said that the 6.5 percent
nonfat solids standard should be
eliminated and replaced with a 2.25
percent protein standard that would
also include whey proteins in
determining if the product meets the
protein standard. The witness stressed
that whey proteins should be
specifically defined as whey proteins
that are a by-product of the cheese
making process. The witness was of the
opinion that adoption of Proposal 7
would not alter the classification of any
product currently being marketed.
The NMPF witness stressed that
Federal order regulations have always
adapted to marketing conditions and
that the current fluid milk product
definition should be amended to reflect
changes in market conditions brought
about by changes in technology. The
witness testified that technology has
evolved such that milk can now be
separated into numerous components
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that can be recombined to create a vast
number of new milk products. The
witness argued that new technology has
enabled manufacturers to manipulate
milk components, such as removing
lactose or substituting whey for other
milk solids, to create new products that
contain less than 6.5 percent nonfat
milk solids. This enables manufacturers
of the new products to avoid
classification of the new product as a
fluid milk product even though the form
and use does not differ from what is
currently considered a fluid milk
product.
The NMPF witness testified that Carb
Countdown®, a product manufactured
by the H.P. Hood Company, contains
whey and has a reduced lactose content
that results in its composition being
below the 6.5 percent nonfat milk solids
standard. According to the witness, two
market research studies suggest that the
product is similar in form and use to
traditional fluid milk. Relying upon a
market study conducted by IRI, a market
research firm, the witness related that
98.4 percent of Carb Countdown® sales
are purchased as a substitute for fluid
milk while only 1 percent of its sales are
represented as an expansion of the fluid
milk market.
The NMPF witness was of the opinion
that classifying a product on the basis of
protein is appropriate because protein is
the highest valued skim component in
the marketplace. The witness testified
that a 2.25 percent protein standard is
the appropriate equivalent of the current
6.5 percent nonfat milk solids standard.
The witness asserted that protein has
the most value to producers, processors
and consumers because it contributes
nutrition, flavor and texture to milk.
While the witness was of the opinion
that all dairy-derived ingredients should
be used in computing the true protein
standard of a product, the witness did
not believe whey and whey product
ingredients should be priced at the Class
I price. The witness maintained that the
use of whey and whey products should
not exclude a product from the fluid
milk product definition because
manufacturers are using whey in their
new products to avoid a fluid milk
product classification. The witness also
noted that instead of relying upon the
Food and Drug Administration (FDA)
standard, the Department should
provide its own definition of whey.
A post-hearing brief submitted on
behalf of NMPF reiterated the positions
testified to at the hearing. The brief
asserted that adoption of a milk protein
standard would close regulatory
loopholes that prevent products
developed as a result of new technology
from avoiding classification as a fluid
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milk product. According to the brief,
adoption of a true protein standard
merely changes the way milk proteins
are accounted for and would not change
the classification of any product.
However, these changes would capture
those products currently formulated to
avoid being classified as fluid milk
products.
Comments and exceptions to the
Recommended Decision filed by NMPF
supported the proposed adoption of the
2.25 percent milk protein standard, the
inclusion of all nonfat milk ingredients
in determining a product’s composition,
and the Class I pricing of milk protein
concentrates (MPCs) used in fluid milk
products. NMPF strongly opposed
exemption of casein and caseinates used
in fluid milk products from Class I
pricing. They view such exemptions as
differential treatment that could cause
market disorder and provide incentives
for manufacturers to use these un-priced
ingredients in their fluid milk products.
NMPF was of the opinion that casein
and caseinates are not substantially
different than MPCs to justify a different
pricing treatment when used in fluid
milk products. However, NMPF
maintained that only whey resulting
from the production of cheese should be
exempted from Class I pricing when
used as an ingredient in fluid milk
products.
NMPF comments and exceptions
asserted that manufacturers have
historically relied on the quantitative
composition standards contained in the
fluid milk product definition when
making decisions regarding new
product development. NMPF expressed
opposition to the proposed reference to
‘‘form and intended use’’ in the fluid
milk product definition because, in
NMPF’s opinion, it could cause
manufacturers to decrease their use of
dairy ingredients in order to prevent a
product from being classified and priced
as a fluid milk product. NMPF urged
abandoning the ‘‘form and intended use’’
standard and relying solely on the
protein and nonfat solids compositional
standards in making classification
decisions.
A witness from DFA, appearing on
behalf of DFA and Dairylea Cooperative,
Inc., (DLC), testified in support of
NMPF’s Proposal 7 and Proposal 2. DLC
is a dairy farmer-member owned
cooperative with 2,400 member farms
located in 7 states at the time of the
hearing.
The DFA/DLC witness was of the
opinion that the purpose of the hearing
was to refine the fluid milk product
definition to reflect current market
conditions brought about by
technological innovations to ensure that
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dairy farmers are equitably paid for their
milk. The witness testified that dairy
processing technology, such as ultra
filtration and milk component
fractionalization, has enabled new
products to be developed that were not
foreseen when the current classification
definition was last considered.
The DFA/DLC witness testified that
the current fluid milk product definition
does not recognize the value of dairy
proteins in the development of new
products and therefore does not classify
and subsequently price these new
products appropriately. The witness
claimed that manufacturers formulate
their products to contain less than 6.5
percent total nonfat milk solids to avoid
a Class I use of milk classification even
though these products compete directly
with and are substitutes for fluid milk.
The DFA/DLC witness was of the
opinion that the form and use of a
product should be the primary factor in
determining product classification. The
witness said that secondary criteria used
to make classification determinations
should include such factors as product
composition, a specific but not
exclusive list of included and excluded
dairy products, product substitutability
and enhancement of producer revenue.
The witness argued that eliminating the
current total nonfat milk solids standard
and replacing it with an equivalent milk
protein standard would better reflect the
demand for dairy proteins in the
marketplace.
The DFA/DLC witness offered a
modification to Proposal 7 that the
witness said would provide the
Department with latitude for classifying
future products that are a result of new
technology. The witness explained that
the modification would allow the
Department to make an interim
classification decision for a new product
and then have up to one year to hold a
public hearing to determine the
appropriate permanent classification.
The DFA/DLC witness also testified in
support of Proposal 2. The witness said
that its adoption would recognize the
importance of dairy proteins in the
marketplace by including all dairy
protein sources, including whey and
whey products, in computing the
product’s protein content. However,
said the witness, while whey and whey
products would be used in classification
determinations, those ingredients
should not be priced as Class I.
A post-hearing brief submitted on
behalf of DFA/DLC reiterated support
for adopting a protein standard. The
brief reiterated the claim that new
technology has enabled some products
that contain less than 6.5 percent nonfat
milk solids to be classified at a lower
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use-value than competitors in the
market. The brief maintained that
adoption of a protein standard would
more adequately identify products that
should be classified as fluid milk
products in light of new fractionation
technology.
A witness appearing on behalf of O–
AT–KA Milk Products Cooperative, Inc.
(O–AT–KA) testified in support of
Proposals 2 and 7. O–AT–KA, at the
time of the hearing, was a cooperative
owned by the dairy farmer-members of
Upstate Farms Cooperative, Inc.,
Niagara Milk Cooperative, Inc., and
Dairylea Cooperative, Inc. The witness
was of the opinion that the development
of new technology necessitates a change
to the fluid milk product definition.
However, the witness cautioned that
changes should not capture all
beverages which contain milk solids as
fluid milk products because not all
milk-containing beverages compete with
fluid milk.
The O–AT–KA witness asserted that
Proposal 7 should not be thought of as
a fundamental change to the current
standard; rather that the proposed true
protein standard of 2.25 percent is an
equivalent to the current 6.5 percent
nonfat milk solids standard and should
be considered as a needed clarification
brought about by technological
advances in milk processing. According
to the witness, the proposed 2.25
percent standard recognizes protein as a
highly valued ingredient in milk
products and those products with less
than 2.25 percent protein would remain
exempt from fluid milk product
classification. The witness also
advocated the adoption of Proposal 2
that would include whey and whey
products in the computation of the
protein percentage of the product but
would not price the whey ingredients at
Class I prices.
A post-hearing brief, submitted on
behalf of O–AT–KA, reiterated support
for Proposal 7. The brief claimed that
the adoption of the protein standard
would increase the use of dairy
ingredients in beverages which are not
‘‘in the competitive sphere of the
traditional milk beverages,’’ thus
increasing producer revenue. The brief
also supported DFA/DLC’s modification
to Proposal 7 giving the Department
authority to make an interim
classification decision if a new product
is a result of new technology.
Comments and exceptions to the
Recommended Decision submitted on
behalf of DFA, DLC, O–AT–KA and
Upstate Farms Cooperative Inc.,
hereinafter referred to as ‘‘DFA, et al.’’,
supported the recommendation
incorporating a 2.25 percent true protein
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standard as a proposal in the
Recommended Decision and that
inclusion of all milk derived ingredients
when computing the 6.5 percent nonfat
solids or 2.25 percent true protein
criterion. The DFA, et al., comments
also endorsed the comments and
exceptions submitted on behalf of
NMPF.
DFA, et al., expressed opposition to
exempting casein and caseinates from
Class I pricing when used in fluid milk
products. The comments argued that all
proteins in a fluid milk product should
be priced the same—at the Class I price.
DFA, et al., also abandoned their
position taken at the hearing to not price
whey derived from cheese making at the
Class I price when used in fluid milk
products. DFA, et al., was of the opinion
that providing exemption for
ingredients will only serve to encourage
manufacturers to use price-exempted
ingredients to formulate a finished
product that would be compositionally
identical to fluid milk.
DFA, et al., took exception to relying
on form and intended use as the final
determinate in classifying fluid milk
products. DFA, et al., argued that
manufacturers rely on the compositional
criteria contained in the fluid milk
product definition to decide how to
formulate a new product, assess how
their new product would be classified,
and ultimately determine their raw milk
ingredient costs. Their exceptions
asserted if form and intended use
criteria supersedes compositional
standards, manufacturers would
develop fewer dairy based products
because of the perceived uncertainty in
how that product’s ingredients could be
classified and priced. DFA, et al., argued
that the 2.25 percent protein standard
should be the ultimate determinate of a
fluid milk product and, if such
compositional standard becomes
inadequate, a hearing could be held to
establish updated compositional
standards.
A post-hearing brief submitted on
behalf of Select Milk Producers, Inc.
(Select) and Continental Dairy Products
(Continental) expressed support for
adoption of a protein standard as a
component of the fluid milk product
definition. According to the brief, Select
and Continental are dairy-farmer owned
cooperatives that market milk on
various Federal orders. The brief argued
that adoption of a protein standard is a
needed change to reflect changed
marketing conditions brought about by
new manufacturing technology without
fundamentally altering current
regulations. The brief stressed that milk
proteins are valuable ingredients in
drinkable products in the market and
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that classification and pricing
determinations should be reflective of
this.
Comments to the Recommended
Decision filed on behalf of Select and
Continental specifically supported the
proposed adoption of a 2.25 percent true
protein standard to the fluid milk
product definition and pricing of MPCs
used in fluid milk products at the Class
I price. Select and Continental also
endorsed the comments and exceptions
filed by NMPF.
Select and Continental’s exceptions
asserted that as a result of new milkprocessing technology, there is no
barrier to using casein as a substitute
ingredient for MPCs. In this regard,
Select and Continental took exception to
exempting casein and caseinates from
Class I pricing because it would serve to
provide an incentive to manufacturers
to use them as a substitute for MPCs to
avoid Class I regulation. The brief said
relying on form and intended use to
override compositional standards in
making classification determinations
would add needless ambiguity and
subjectivity.
A witness appearing on behalf of H.P.
Hood testified in opposition to any
changes to the fluid milk product
definition. The witness was of the
opinion that the fluid milk product
definition should not be amended in a
manner that would classify more dairy
products as fluid milk products unless
data is provided which would conclude
that such products compete directly
with fluid milk and such amendments
would enhance producer revenue.
The H.P. Hood witness asserted that
if Proposal 7 was adopted and resulted
in the reclassification of some products
as fluid milk products, the change
would only affect a small number of
products and the enhancement of
producer revenue would be minimal. If
ingredient substitution for milk
occurred as a result of adopting other
proposals, the witness said, producer
revenue could actually decrease. The
witness was of the opinion that
adoption of proposals that broaden the
fluid milk product definition would
stifle product innovation and discourage
the use of dairy-derived ingredients
because of the resulting increased costs
to the manufacturer. These results, the
witness said, should not be encouraged
by the Federal milk order program.
A post-hearing brief submitted on
behalf of H.P. Hood reiterated
opposition to Proposal 7. The brief
maintained that no disorderly marketing
conditions exist to warrant a change to
the fluid milk product definition and
that proponents of the protein standard
failed to meet the burden of proof
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required by the AMAA to make a
regulatory change. The H.P. Hood brief
reviewed many factors used by the
Department in previous classification
decisions to determine the proper
classification of Class I products. The
list included, but was not limited to,
demand elasticities, enhancement of
producer revenue, and product
competition. The brief stated that
proponents failed to provide adequate
data addressing these factors or prove
that disorderly marketing conditions
exist to warrant a change, and urged the
Department to terminate the proceeding.
Comments and exceptions filed by
H.P. Hood took exception to the
Recommended Decision’s proposed
adoption of a 2.25 percent protein
standard and its reliance on form and
intended use as a primary factor in
making classification determinations.
H.P. Hood reiterated its opinion that the
proponents of the protein standard did
not provide adequate justification for its
adoption. Furthermore, H.P. Hood was
of the opinion that it is not proper to
make regulatory changes as preventive
measures to possible disorderly
marketing conditions and is a major
deviation from historical milk order
policy. The exceptions stressed that it is
only proper to react to marketing
conditions once they occur. In their
exceptions, H.P. Hood also presented a
list of questions regarding the
application of how a product’s form and
intended use would be determined by
the Department. H.P. Hood claimed that
relying on form and intended use would
be extremely burdensome and serve to
inhibit new product development.
A witness appearing on behalf of
Leprino Foods Company (Leprino)
testified in opposition to the adoption of
the 2.25 percent protein standard
contained in Proposal 7. According to
the witness, Leprino operates nine
plants in the United States that
manufacture mozzarella cheese and
whey products. The witness was of the
opinion that a protein standard would
reclassify products such as sport and
protein drinks and yogurt smoothie
products (formulated with ingredients
such as whey and whey products) as
fluid milk products. The witness
stressed that broadening the fluid milk
product definition to account for all
dairy derived ingredients could lessen
the demand for such ingredients. The
witness speculated that manufacturers
may seek out other less costly non-dairy
ingredient substitutes which would
result in decreased producer revenue.
Exceptions to the Recommended
Decision filed by Leprino expressed
opposition to the adoption of a 2.25 true
protein standard in the fluid milk
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product definition. Leprino argued that
this standard should not be adopted
unless it is modified to specifically
exclude beverages that do not resemble
or compete with fluid milk. Leprino was
of the opinion, that without such
exclusion, to classify products based on
form and intended use could cause
many non-traditional products, such as
sport and nutritional beverages, to be
classified as fluid milk products. The
end result, argued Leprino, would be a
lowered demand for dairy ingredients
that may offset any revenue gains to
producers by including additional
products as fluid milk products.
A witness appearing on behalf of
Dannon Company, Inc. (Dannon)
testified in opposition to Proposals 2
and 7. Dannon is a wholly owned
subsidiary of the Dannon Group that
produces yogurt and fresh dairy
products in 40 countries, including the
United States. The witness was opposed
to the adoption of a protein standard
and to the inclusion of whey when
calculating the nonfat milk solids
content of a product because, the
witness said, it was not the original
intent of the fluid milk product
definition to include these milk-derived
ingredients. The witness believed that
adoption of a protein standard would
cause more products to be classified as
fluid milk products even though they do
not compete with fluid milk. The
witness argued that protein is not a
major component of fluid milk products
and therefore using a protein standard
would not be appropriate for making
classification determinations. The
witness speculated that if a protein
standard was adopted, it could stifle
product innovation or cause food
processors to use non-dairy ingredients
in their food products. The witness said
that if whey proteins are included,
manufacturers may look for less
expensive non-dairy ingredients to be
used as a viable substitute.
A post-hearing brief submitted on
behalf of Dannon reiterated their
opposition to the adoption of a protein
standard claiming that adequate
justification for such a change was not
given by proponents at the hearing and
that the mere ability to test for milk
proteins does not justify its adoption.
A post-hearing brief submitted on
behalf of the National Yogurt
Association (NYA) expressed opposition
to Proposal 7. According to the brief,
NYA is a trade association representing
manufacturers of live and active culture
yogurt products and suppliers of the
yogurt industry. The brief claimed that
proponent testimony was inconsistent
regarding the proposals’ impact on
product classification and stated that if
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the 2.25 percent protein standard was
adopted, at least one yogurt-containing
product would be reclassified as a fluid
milk product.
The NYA brief also asserted that
proponents did not provide a clear
picture of how Proposal 7 would be
implemented. Specifically, the brief
noted that the following were not
addressed: (1) How wet and dry whey
would be handled; (2) how whey from
cheese production would be
differentiated from whey from casein
production; and (3) how products that
meet the proposed 2.25 percent true
protein standard and contain whey and
other proteins would be classified and
priced. The NYA brief speculated that
including whey in the protein
calculation would lead to more products
being classified as fluid milk products
and cause manufacturers to seek out less
costly non-dairy ingredients. The
potential loss to producer revenue by
substitution with non-dairy ingredients,
concluded the brief, is not supported by
the record.
A post-hearing brief submitted on
behalf of the National Cheese Institute
(NCI) expressed opposition to Proposal
7 and claimed that its adoption would
suppress the use of dairy-derived
ingredients, particularly whey proteins.
According to the brief, NCI is a trade
association representing processors,
manufacturers, marketers, and
distributors of cheese and related
products. NCI claimed that proponents
of Proposal 7 did not identify any
specific marketplace disorder that
would be corrected by the adoption of
a protein standard or list any product
that would be reclassified if the fluid
milk product definition were amended.
The brief reviewed previous rulemaking
decisions where proposals were denied
because proponents failed to
demonstrate that disorderly marketing
conditions were present.
The NCI brief stressed that use of
dairy-derived ingredients in a product
should not automatically qualify a
product as a competitor of fluid milk or
that their classification in a lowervalued use negatively affects producer
revenue. The brief further maintained
that proponents did not adequately
address why whey proteins should be
included in determining if the product
met the proposed protein standard for a
fluid milk product and why whey
should be priced at the Class I price.
The brief concluded that whey should
be excluded from the fluid milk product
definition because its inclusion would
lead to products being classified as fluid
milk products even when they do not
compete with fluid milk.
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A post-hearing brief submitted on
behalf of Sorrento Lactalis, Inc.
(Sorrento) objected to the adoption of a
protein standard. According to the brief,
Sorrento is a manufacturer that operates
five cheese plants throughout the
United States. The brief stated that
adoption of a milk protein standard as
part of the fluid milk product definition
would reduce the demand for dairy
ingredients, especially whey proteins,
which in turn would result in increased
costs to manufacturers and reduced
producer revenue.
A witness testifying on behalf of H.P.
Hood was of the opinion that if the
Department found that changing the
fluid milk product definition was
warranted, adoption of a modified
Proposal 5 would be appropriate. The
witness said that adoption of Proposal 5
would provide the Department with
standards to determine if a dairy
product with less than 6.5 percent
nonfat milk solids competes with and
displaces fluid milk sales, which would
justify classification of the product as a
fluid milk product. The witness also
noted that if Proposal 5 was adopted, a
new product with less than 6.5 percent
nonfat milk solids and route
distribution in a Federal milk marketing
area of less than 3 million pounds
would be exempted from classification
as a fluid milk product. This
distribution criteria, the witness
explained, would allow manufacturers
to test market a new product with the
assurance that it would not be classified
as a fluid milk product until the
distribution threshold was exceeded.
A witness appearing on behalf of
Leprino testified in support of Proposal
5. The witness was of the opinion that
fluid milk products should only be
those products that meet the FDA
standard of identity for milk and
cultured buttermilk and products that
compete with milk and cultured
buttermilk. The witness testified that
the fluid milk product definition is
currently too broad and as a result, has
lessened the demand for dairy
ingredients in new non-traditional dairy
products because of the possibility of
being classified as a fluid milk product.
The witness argued that many of these
new products do not compete for sales
with fluid milk and their use of dairyderived ingredients should not qualify
them to be defined as a fluid milk
product.
The Leprino witness explained that
advances in technology have allowed
the creation of dairy-derived ingredients
through milk fractionation. According to
the witness, dairy manufacturers are
avoiding investing in some product
innovation because of the regulatory
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burden and increased costs that are
associated with manufacturing a fluid
milk product.
A witness testifying on behalf of DFA/
DLC was opposed to the adoption of
Proposal 5. The witness said that
Proposal 5 would place an undue
burden on the Department in making
classification determinations and would
also extend Class II classification to
more products, neither of which the
witness supported. The post-hearing
brief submitted by DFA/DLC reiterated
their opposition.
A witness appearing on behalf of
Bravo! Foods International Corporation;
Lifeway Foods, Inc.; PepsiCo; Starbucks
Corporation; and Unilever United
States, Inc.; testified in opposition to all
proposals that would reduce or
eliminate the 6.5 percent minimum
nonfat milk solids standard, adopt a
protein standard, or include whey in
determining the nonfat milk solids
content of a product. Hereinafter, these
companies are referred to collectively as
‘‘Bravo!, et al.’’
A post-hearing brief submitted on
behalf of Bravo!, et al., urged the
termination of the proceeding except for
the portion addressing the exemption of
yogurt and kefir products from the fluid
milk product definition. Bravo!, et al.,
asserted that the hearing record does not
support adoption of a protein standard.
The brief stated that decisions to amend
Federal order provisions are not made
without clear evidence of disorderly
market conditions, the potential
shortage of milk for fluid use, or
lowering of producer revenue. The brief
also discussed letters sent to the
Department by producers and
manufacturers which urged that a
hearing be postponed because more
analysis and market data was needed to
justify amending the current fluid milk
product definition. Bravo!, et al., argued
that the hearing was held prematurely,
without allowing for adequate study and
market data research on the proposals
that are under consideration. According
to the brief, more time was needed to
accurately determine the impact of new
milk products on the marketplace.
The Bravo!, et al., brief summarized
hearing testimony from previous
Department rulemaking decisions in
which no changes were recommended
due to a lack of evidence to support a
regulatory change. According to Bravo!,
et al., proponents did not provide
evidence of disorder in the marketplace
nor did they substantiate their claims
that products currently in the market
would not be reclassified if a protein
standard was adopted. On the basis of
such conditions, the brief concluded
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that the current fluid milk product
definition is adequate.
If the Department did not terminate
the proceeding, the Bravo!, et al., brief
recommended that the 6.5 percent
nonfat milk solids standards remain,
that the computation of nonfat milk
solids not be made on a milk
equivalency basis, and that whey and
whey ingredients be excluded from the
computation.
Exceptions to the Recommended
Decision filed by Bravo!, et al., opposed
the proposed adoption of the 2.25
percent protein compositional standard
and reiterated that adoption of a protein
standard would have a negative effect
on dairy product innovation as
manufacturers would use lower priced
non-dairy proteins as substitutes.
Bravo!, et al., asserted that the
Department did not give enough
consideration to the lowering of
producer revenue that could occur due
to the predicted ingredient substitution.
Exceptions filed by Bravo!, et al., also
opposed the Department’s use of form
and intended use as one of the factors
in making classification determinations.
The comments acknowledged that the
AMAA authorized the Federal Milk
Marketing Order (FMMO) program to
rely on form and intended use in
making classification determinations.
However, Bravo!, et al., asserted that
historically the FMMO program applied
the form and use criteria by using
compositional standards. Bravo!, et al.,
claimed that by specifically including
the form and intended use criteria in the
order language the Department could
ignore a product’s composition and
arbitrarily classify products as fluid
milk products even though they did not
compete with fluid milk. Bravo!, et al.,
predicted that the specific inclusion of
form and intended use in the fluid milk
product definition would hamper the
development of new products and the
use of dairy ingredients because of the
uncertainty manufacturers could face in
how the milk components of their
products would be classified.
A witness appearing on behalf of
Fonterra USA, Inc. (Fonterra) testified in
opposition to proposals that would
include MPCs in determining if the
product met the protein standard of the
fluid milk product definition. Fonterra
at the time of the hearing was a wholly
owned subsidiary of Fonterra Cooperative Group Limited, a New
Zealand based dairy cooperative owned
by 12,000 New Zealand dairy farmers.
Fonterra operates plants within the
United States that produce, among other
things, MPCs. The witness stressed that
changes to the fluid milk product
definition would increase ingredient
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costs, discourage manufacturing
companies from using dairy ingredients
in their products, and force those
companies to seek other less costly
substitutes such as soy and soy
products.
A post-hearing brief submitted on
behalf of Fonterra reiterated their
objection to changing the nonfat milk
solids standard and predicted that
adoption of a protein standard would
make classification decisions
unnecessarily complicated without
providing additional benefits to
producers. The brief asserted that the
hearing record did not contain a
sufficient economic analysis on the
possible benefits that adopting a protein
standard would have on producer
revenue or its impact on the dairy
industry.
The Fonterra brief speculated that
adoption of a milk protein standard
would decrease the market price for
milk proteins, discourage new product
development, and encourage the
substitution of producer milk with nondairy ingredients. The brief noted that
the annual growth rate of soy and soy
products in nutritional products from
1999 to 2003 was 16.5 percent, while
the growth of milk proteins in
nutritional products only increased 10.1
percent over the same time period. The
brief predicted that if protein prices rise
as a result of the adoption of a milk
protein standard, the growth of soy
proteins will likely increase because
they could be substituted for more
costly milk proteins.
The Fonterra brief also stated that the
hearing record does not reveal disorder
in the market by the application of the
current fluid milk product definition
and therefore concluded that amending
the fluid milk product definition is not
justified. The Fonterra brief argued that
proponents did not provide adequate
reasoning for including whey proteins
in determining if a product met the
protein standard but not pricing whey
proteins the same as other milk
proteins. Furthermore, the brief stated
that proponents did not propose a
method for differentiating between
whey proteins resulting from cheese
production and whey proteins from
other sources.
Comments filed on behalf of Fonterra
took exception to the Recommended
Decision’s proposed adoption of a 2.25
percent true milk protein compositional
standard. Fonterra reiterated that
proponents did not meet the burden of
proof needed to substantiate the
adoption of a protein standard.
According to the comments, proponents
did not indicate if adoption of the
standard would remedy any indications
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of market disruption or reclassify some
products as fluid milk products.
Fonterra’s comments reviewed
numerous rulemaking proceedings in
which, Fonterra concluded, the
Department declined to adopt proposed
changes to marketing orders because of
a lack of evidence that a change would
promote orderly marketing conditions.
Fonterra argued that the Recommended
Decision did not adequately consider
evidence asserting that adoption of the
milk protein standard would not
increase the cost for dairy ingredients,
encourage the substitution of lower cost
non-dairy ingredients, and ultimately
lower producer revenue. Fonterra was of
the opinion that before making a Final
Decision, further analysis of the
proposals was needed to fully evaluate
the possible economic impact to
producers and manufacturers as a result
of adoption of the protein standard.
Fonterra stated that the Department’s
recommended adoption of an ‘‘either/or’’
use of the protein and nonfat solids
standard was not contained in any
proposal discussed at the hearing and
that the Department did not adequately
explain how the use of both a protein
and nonfat solids standard would
provide for the orderly marketing of
milk or increase producer revenue.
The comments filed by Fonterra also
argued that the Department uses this
rulemaking proceeding to justify a
change in policy that the Department
previously attempted to adopt without
undertaking the formal rulemaking
process. Fonterra stated that historical
Departmental policy has been to exempt
such products as casein, sodium
caseinate, lactose, whey, and MPCs from
use in the nonfat milk solids calculation
of a product. In 2004, Fonterra said, the
Department attempted to include MPCs
and other previously exempted dairy
ingredients in the nonfat solids
calculation; however, that
administrative decision was overturned
by an Administrative Law Judge.
Fonterra claimed that proposing to
include all milk derived protein
ingredients in the calculation of a
product’s nonfat solids or protein
composition is an attempt to change
historical policy without adequate
analysis or justification.
Fonterra also took exception to having
some ingredients included in the
calculation of a product’s composition
but would not be priced in a final
product. Fonterra claimed that whey is
used in nearly identical products as
MPCs and should therefore be priced
the same. Fonterra was of the opinion
that pricing whey and MPCs differently
would violate the United States’ World
Trade Organization obligations. Fonterra
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characterized whey production as
primarily domestic, but that most MPCs
are imported. Accordingly, they
concluded that excluding whey from
Class I pricing essentially places an
illegal tariff on imported MPCs.
A witness appearing on behalf of the
American Beverage Association (ABA)
testified in opposition to all proposals
seeking to amend the fluid milk product
definition. ABA is a trade association
that represents beverage producers,
distributors, franchise companies, and
their supporting industries. The witness
was of the opinion that the current fluid
milk product definition already
properly classifies dairy products and
that there is insufficient evidence to
warrant any changes. The witness
claimed that any change would broaden
the fluid milk product definition to
include products that contain only
small amounts of milk. The witness
argued that many new beverage
products which contain small amounts
of milk or milk ingredients do not
compete with fluid milk but do compete
with soft drinks, juices and bottled
water. The witness asserted that
amending the fluid milk product
definition to include some dairy
ingredients not currently considered
would increase manufacturers cost of
production, result in stifled innovation
of new products and encourage the use
of non-dairy ingredients as substitutes
for milk-derived ingredients.
A witness appearing on behalf of Ohio
Farmers Union (OFU) testified in
opposition to any change to the fluid
milk product definition. OFU is a
nonpartisan, grassroots, general farm
organization representing more than
300,000 family farms nationwide
according to their web site. The witness
testified that the primary purpose of the
order program was to provide
consumers with a reliable supply of safe
and wholesome milk. The witness
asserted that MPCs, caseinates, whey
proteins, and other similar milk-derived
ingredients have functional and
nutritional characteristics different than
fluid milk. Accounting for those
ingredients in the fluid milk product
definition, the witness said, would
undermine the goal of the order
program. The witness stressed that if the
fluid milk product definition were
amended, consumer confidence in the
long established perception of milk as a
fresh, pure and wholesome beverage
would be diminished and would thus
threaten the economic viability of
domestic producers.
A witness appearing on behalf of the
Milk Industry Foundation (MIF)
testified in opposition to amending the
fluid milk product definition. According
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to the witness, MIF is an organization
with over 100 member companies that
process and market approximately 85
percent of the fluid milk and fluid milk
products consumed nationwide. The
witness stated that simply because a
beverage contains milk or other dairyderived ingredients does not prove that
those products compete with fluid milk
or that such competition lowers
producer revenue.
The MIF witness asserted that
previous Federal milk order rulemaking
decisions have required data and
analysis to prove that an amendment
was warranted. According to the
witness, the proponents of proposals for
changing the fluid milk product
definition did not provide such data and
analysis. Along this theme, the witness
said that proponents should have
provided data such as the market share
held by products that do not fall under
the current fluid milk product definition
but would be included under any
proposed change, cross price elasticity
of demand analysis of products which
meet the existing fluid milk product
definition and of products that would be
classified as a fluid milk product if any
of their proposals were adopted, and an
own-price elasticity of demand analysis
for products that would be reclassified.
A post-hearing brief submitted on
behalf of MIF reiterated their opposition
to any changes to the current fluid milk
product definition. The brief urged that
if the Department does amend the fluid
milk product definition, it should
exclude all whey-derived protein
products in determining if a product
meets the fluid milk product definition.
The brief stated that MIF has
continuously opposed a hearing to
consider amending the fluid milk
product definition because not enough
evidence is available to warrant a
change. The brief maintained that
proponents did not offer adequate data
at the hearing to demonstrate that there
is disorder in the marketplace that can
be remedied by adoption of a protein
standard.
The MIF brief expanded its testimony
by citing numerous rulemaking
decisions that denied proposals on the
basis that adequate evidence was not
presented to warrant amendments to
order provisions. MIF stressed that the
mere existence of beverages containing
dairy-derived ingredients is not
evidence of marketwide disorder.
Exceptions filed on behalf of
International Dairy Foods Association
(IDFA) asserted that because evidence
doesn’t demonstrate a need for change,
no changes to the fluid milk product
definition should be made. IDFA is a
trade organization whose members
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33541
include MIF, NCI and the International
Ice Cream Association (IICA). According
to their exceptions, IDFA represents
more than 85 percent of the milk,
cultured products, cheese and frozen
desserts produced and marketed in the
United States. IDFA reiterated
arguments expressed by MIF at the
hearing and in MIF’s post-hearing brief.
Their exception claimed that the
hearing record did not demonstrate that
products containing less than 6.5
percent nonfat solids and more than
2.25 percent protein are causing
disorderly marketing conditions because
they are not currently classified as fluid
milk products.
IDFA’s comments also opposed the
specific inclusion of the form and
intended use criteria in the fluid milk
product definition and argued that the
definition should continue to contain
only compositional criteria. IDFA wrote
that manufacturers’ product
development decisions are in part
determined by ingredient costs.
Subjective criteria such as form and
intended use, wrote IDFA, could
impede new product development
because a manufacturer would be
uncertain of ingredient costs until a
final product had been classified.
IDFA’s exceptions opposed the
inclusion of whey when computing a
product’s composition because of
inconsistent justification by proponents
as to why whey used to produce fluid
milk products should not also be priced
as Class I. IDFA exceptions stated that
the proponents of the protein standard
did not demonstrate that disorderly
marketing conditions exist in the
absence of the protein standard. IDFA
exceptions concluded that the adoption
of amendments proposed in the
Recommended Decision would only
serve to lower producer revenue.
Comments filed on behalf of Grande
Cheese opposed all the proposed
changes to the fluid milk product
definition contained in the
Recommended Decision. Grande Cheese
is a cheese manufacturer located in the
State of Wisconsin. Grande Cheese
expressed support of the opinions
expressed in the exceptions to the
Recommended Decision filed by IDFA.
A witness appearing on behalf of the
National Family Farm Coalition testified
in opposition to all proposals that
would amend the fluid milk product
definition. The witness testified that
MPCs do not meet FDA’s Generally
Recognized as Safe (GRAS) standards as
legal food ingredients. Furthermore, the
witness said, MPCs have not been
subjected to scientific testing to
determine if they are safe for human
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consumption and should not be allowed
in milk products.
A witness appearing on behalf of
Public Citizen testified in opposition to
proposals that seek to amend the fluid
milk product definition. According to
the witness, Public Citizen is a nonprofit consumer advocacy organization
with approximately 150,000 members.
The witness was opposed to any change
in the fluid milk product definition that
would, in the witness’ opinion,
encourage the use of MPCs.
Two Pennsylvania dairy farmers
testified in opposition to any change to
the fluid milk product definition. The
producers opposed all proposals that
would allow the use of caseinates and
MPCs in fluid milk products. They
asserted that MPCs are not allowed in
the production of standardized cheese
and should also not be allowed in the
production of fluid milk products.
A post-hearing brief submitted on
behalf of the American Dairy Products
Institute (ADPI), an association
representing manufacturers of dairy
products, offered support for amending
the fluid milk product definition to
include milk beverages that compete
directly with fluid milk. However, the
brief cautioned against developing a
fluid milk product definition that would
include non-traditional beverages and
smoothie type products (yogurtcontaining beverages). The brief
recommended that an economic study
be conducted to determine the possible
impacts of the proposed changes before
action is taken to amend the fluid milk
product definition.
A post-hearing brief submitted on
behalf of General Mills contended that
the fluid milk product definition should
not be amended because proponents did
not provide sufficient evidence or data
to justify a change. The brief maintained
that the hearing record is not clear on
how proposals would be implemented
or on the impact to producers,
manufacturers, and consumers if the
protein standard was adopted. General
Mills contended that before a change is
made, the Department should conduct
an economic analysis to evaluate how
protein and dairy products are
competing in the marketplace and how
the adoption of a protein standard
would impact the marketplace. If a
protein standard was recommended for
adoption, General Mills recommended
that whey not be included in the protein
calculation, or if whey is included, that
a 2.8 percent protein standard be
adopted in order to maintain the status
quo.
Exceptions to the Recommended
Decision filed by General Mills opposed
the adoption of the true protein
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compositional standard. However,
General Mills was of the opinion that if
the Department continued to support
the protein standard, then any whey
components should be excluded from
determining a final product’s protein
content. General Mills purported that
the inclusion of whey in the protein
calculation, even if not priced at Class
I, may lead manufacturers to increase
their use of non-dairy ingredients as
substitutes.
General Mills was also opposed to
relying on form and intended use in
classification determinations. According
to their exceptions, the form and use
criteria would cause manufacturers to
be less certain of a product’s
classification which would discourage
using dairy ingredients in new products.
General Mills noted that if the
Department decides to not alter its
Recommended Decision then it should
clarify in a Final Decision that only
products that compete with or are a
substitute for fluid milk would be
classified as a fluid milk product.
A post-hearing brief submitted on
behalf of New York State Dairy Foods,
Inc. (NYSDF) opposed amending the
fluid milk product definition. According
to their brief, NYSDF is a trade
association representing dairy product
processors, manufacturers, distributors,
retailers, and producers in the Northeast
United States. The brief argued that
products produced with the use of new
fractionation technology are a small
portion of the milk beverage market.
They were of the opinion that such
products are still too new to determine
their impact on Class I sales and
producer revenue. The brief also
asserted that the adoption of a protein
standard as part of the fluid milk
product definition would discourage
new product development and would
increase costs that would result in
reduced sales of dairy-derived
ingredients. The brief urged that the
proceeding be terminated.
Comments and exceptions to the
Recommended Decision filed on behalf
of Glanbia Foods (Glanbia) opposed the
proposed adoption of the true protein
compositional standard and the specific
inclusion of form and intended use as
a factor in classification determinations.
Glanbia operates two cheese plants and
two whey plants that collectively
process nearly 4 billion pounds of milk
annually. Glanbia asserted that adoption
of a true protein standard would lead to
stifled innovation of milk derived
ingredients in new products because the
manufacturing industry would increase
its use of non-dairy ingredients as
substitutes. Their exceptions claimed
that the hearing record does not contain
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evidence that adoption of a protein
standard would ultimately benefit
producers or remedy a market disorder.
Glanbia also argued that the
Department’s reliance on form and
intended use in classification
determinations would similarly
discourage the use of dairy ingredients.
A professor from Cornell University
testified regarding a research study
conducted by the Cornell Program on
Dairy Markets and Policy that focused
on the demand elasticity’s of various
dairy products. The witness did not
appear in support of or in opposition to
any proposal presented at the hearing.
The witness explained that the goal of
the study was to ascertain the extent to
which product innovation and
classification decisions influence
producer revenue. The study was
designed to evaluate four hypothetical
dairy products and test the effect that a
range of classification determinations
would have on producer revenue. The
witness explained the study and
concluded that the impact on producer
revenue of a new product being
reclassified from Class II to Class I was
likely to be small, plus-or-minus $0.01
per hundredweight (cwt). However, the
witness added, if non-dairy ingredients
were substituted as a result of the
reclassification, the study predicted that
producer revenue would be lowered by
$0.22 per cwt. The witness concluded
that while the financial returns from
product reclassification could be
positive, the resulting ingredient
substitution, which could take place,
would result in a significant negative
impact on producer revenue.
The post-hearing brief submitted by
NMPF also addressed concerns
articulated at the hearing regarding the
need for a demand elasticity study to
address the issue of product substitution
before amending the fluid milk product
definition. The brief asserted that a
demand elasticity study would not take
into account newly emerging products,
changing consumer preferences, and
product innovations that could change
the competitive relationships between
products and therefore would not
provide any relevant data. The brief also
argued that the economic model created
by Cornell University and discussed at
the hearing contained many incorrect
assumptions and thus concluded that
the study results were flawed.
The DFA/DLC brief also rebutted
opposition to Proposal 7 which called
for studies of product usage or demand
elasticity’s before considering
amendments to the fluid milk product
definition. The brief asserted the
previous amendments to the
classification system have been made
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without such economic studies and that
this proceeding should be handled in
the same manner.
A witness appearing on behalf of
Bravo! Foods International Corporation,
Lifeway Foods, Inc. (the principal
makers of kefir in the U.S.), PepsiCo,
Starbucks Corporation and Unilever
United States, Inc. (Bravo! et al.),
proposed at the hearing that kefir, as
well as yogurt-containing beverages, be
exempted from the fluid milk product
definition.
A witness appearing on behalf of
Dannon testified in support of Proposal
8 that would exclude yogurt containing
beverages from the fluid milk product
definition. The witness provided a
definition of yogurt containing
beverages as any beverage containing at
least 20 percent yogurt (which is in
concert with Proposal 9). The witness
argued that yogurt containing beverages
are not similar in form and use to fluid
milk products and should be excluded
from the fluid milk product definition.
The witness testified that Dannon
currently manufactures yogurt
containing products which are classified
as both fluid milk products and Class II
products. The Dannon witness
maintained that regardless of the
classification, none of its products
compete with fluid milk. According to
the witness these products should all be
classified as Class II. The witness
emphasized that yogurt and yogurtcontaining products use unique
cultures, ingredients, and production
technology that differentiate them from
fluid milk product production.
Furthermore, the witness said yogurt
products’ packaging, taste, mouth feel,
shelf-life and marketing placement in
grocery stores distinguishes them from
fluid milk.
The Dannon witness presented market
research it had conducted. The witness
stated, based on the research, that
yogurt-containing beverages are
consumed as a food product and not as
an alternative to fluid milk. The witness
claimed that less than one percent of
potential consumers of a Dannon
yogurt-containing product consume the
product as a substitute for fluid milk.
Additionally, the witness noted that
Dannon advertises its yogurt-containing
products as a substitute for snacks, not
fluid milk. The witness concluded from
this that yogurt-containing products are
different than fluid milk, do not
compete with fluid milk in the
marketplace and therefore should not be
classified the same as a fluid milk
product. The witness also testified in
opposition to Proposal 9 but only with
respect to the inclusion of a protein
threshold which Dannon does not
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consider justified. The witness noted
that Dannon does support the proposed
20 percent minimum yogurt content
standard that such products should
meet as a condition for being exempted
from the fluid milk product definition.
A post-hearing brief submitted on
behalf of Dannon reiterated its hearing
testimony. The brief stated that fluid
milk products should only be those
products that are closely related to, or
compete with, fluid milk for sales. That
brief stressed that yogurt-containing
beverages are dissimilar to fluid milk
beverages and are used as a food
replacement, not as a beverage
substitute. The brief noted that in 2004,
more than 37 percent of Dannon’s sales
were from products developed within
the last 5 years and stressed that
classifying all milk drinks with milkderived ingredients as fluid milk
products would result in decreased
innovation for developing additional
uses for milk.
A witness appearing on behalf of
General Mills testified in support of
Proposal 9. The witness was of the
opinion that USDA should classify
products primarily on the basis of form
and use. The witness asserted that
drinkable yogurt products, while
containing milk ingredients, are food
products and do not compete with fluid
milk. The witness explained that
drinkable yogurt products were created
to meet a change in consumer
preferences for convenience and
portability. The witness presented
market research conducted by Yoplait
demonstrating that consumers view
drinkable yogurt products as
alternatives to traditionally packaged
yogurt and other nutritional snacks, not
fluid milk. The witness asserted that 80
percent of Yoplait drinkable yogurt
smoothie consumers would substitute
another yogurt product for the smoothie.
The General Mills witness supported
the current classification system
contending that its modification raises a
host of issues and questions. However,
if USDA determined that a change to the
fluid milk product definition is
appropriate, the witness urged adoption
of Proposal 9 to exclude drinkable
yogurt products that contain at least 20
percent yogurt by weight and no more
than 2.2 percent skim milk protein from
the fluid milk product definition.
According to the witness, including
drinkable yogurt products in the fluid
milk product definition would increase
costs to manufacturers that would stifle
innovation and result in a shift towards
using non-dairy ingredients. The
witness said manufacturers would
choose to reformulate products using
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less milk and milk proteins resulting in
reduced dairy producer income.
A post-hearing brief submitted on
behalf of General Mills maintained that
ample evidence regarding the
fundamental differences of fluid milk
and yogurt containing beverages was
presented at the hearing to justify
exempting yogurt containing products
with more than 20 percent yogurt from
classification as a fluid milk product.
Comments and exceptions to the
Recommended Decision filed on behalf
of General Mills reiterated this view.
Two witnesses appearing on behalf of
the National Yogurt Association (NYA)
testified in support of proposals that
would exempt yogurt containing
products from the fluid milk product
definition. NYA is a national trade
association representing the producers
of yogurt products and their suppliers.
The witnesses testified that previous
regulatory decisions made by USDA
emphasized that products classified as
fluid milk products should be intended
to be consumed as beverages and
compete with fluid milk. The witnesses
expressed disagreement with a
classification decision published in the
early 1990’s that classified drinkable
yogurt products as fluid milk products.
The witnesses were of the opinion that
in both form and use, yogurt and
drinkable yogurt products compete with
other food products, not fluid milk, and
should be classified as Class II products.
The witnesses explained that yogurt
products are produced and shipped
nationally by a few manufacturers, have
a shelf-life averaging 30–60 days, have
a texture and taste distinctly different
than fluid milk and are positioned in
retail stores separate from fluid milk.
The witnesses noted that yogurtcontaining beverages were developed as
a substitute for spoonable yogurt
products, not fluid milk.
The NYA witnesses were of the
opinion that the increase in producer
revenue resulting from currently
classifying drinkable yogurt products as
fluid milk products isn’t and would not
overcome the decrease in revenue due
to the loss of sales from an increase in
the price of drinkable yogurt products.
A post-hearing brief submitted on
behalf of NYA reiterated support for
excluding all products containing at
least 20 percent yogurt provided that the
yogurt meets the standard of identity for
yogurt. According to the brief, the 20
percent content requirement would
ensure that only products whose
characterizing ingredient is yogurt
would be excluded from the fluid milk
product definition. The brief also
indicated that if USDA determines not
to exclude yogurt containing products,
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then NYA strongly opposes any change
to the current fluid milk product
definition.
The NYA brief argued that consumer
surveys and marketplace data provided
by Dannon and General Mills that
explained how yogurt-containing
products are fundamentally different
from fluid milk were not contradicted at
the hearing. The brief also noted that
while Dairy Farmers of America (DFA)
and National Milk Producers Federation
(NMPF) testified that consumers are
buying low-carbohydrate milk instead of
fluid milk, they did not offer similar
evidence for yogurt-containing
products.
Comments and exceptions to the
Recommended Decision filed on behalf
of NYA supported the proposed
exemption of drinkable yogurt products
from the fluid milk product definition.
The NYA comments reiterated
arguments it made at the hearing and in
its post-hearing brief, and asserted that
the hearing record contains no evidence
to support that drinkable yogurt
products are similar to fluid milk.
A witness appearing on behalf of
Bravo!, et al., testified in support of
amendments that would exempt yogurt
containing products and kefir from the
fluid milk product definition. The
witness argued that both products are
compositionally different than fluid
milk and do not compete for sales with
fluid milk. Furthermore, the witness
noted that drinkable yogurt and kefir
products are one of the fastest growing
segments in the dairy industry,
providing a large opportunity for the
expanded use of dairy-derived
ingredients which should not be
hampered by the additional costs of
such ingredients being priced at Class I.
Comments and exceptions filed on
behalf of Bravo!, et al. and by Lifeway
Foods, separately expressed support for
the Recommended Decision’s proposed
exemption of kefir, and drinkable yogurt
products that contain at least 20 percent
yogurt.
A witness appearing on behalf of
Leprino Foods Company (Leprino)
testified that if USDA recommended
amending the fluid milk product
definition, then Leprino supported the
adoption of Proposal 9 to exclude
products containing at least 20 percent
or more yogurt by weight from the fluid
milk product definition. According to
the witness, Leprino operates nine
plants in the United States that
manufacture mozzarella cheese and
whey products. The witness also was of
the opinion that yogurt containing
products do not compete with fluid
milk and should be classified as Class
II products. The witness stressed that if
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these products are not excluded from
the fluid milk product definition, then
Leprino strongly opposed the adoption
of a protein standard to be part of the
fluid milk product definition.
Comments and exceptions filed on
behalf of Leprino supported the
Recommended Decision’s proposed
exclusion of yogurt containing
beverages and kefir from the fluid milk
product definition.
Comments filed by Fonterra USA, Inc.
(Fonterra) supported the Department’s
recommendation that yogurt containing
beverages should be exempted from the
fluid milk product definition but took
exception to the yogurt content in
beverages containing less that 20
percent yogurt (i.e. Class I) not being
subject to an ‘‘upcharge’’, as are other
milk ingredients. Fonterra is a wholly
owned subsidiary of Fonterra Cooperative Group Limited, a New
Zealand based dairy cooperative owned
by 12,000 New Zealand dairy farmers.
The witness appearing on behalf of
NMPF testified in opposition to
exempting yogurt-containing beverages
from the fluid milk product definition.
The witness was of the opinion that
these products are similar in form and
use to other flavored fluid milk products
and should be considered a substitute
for fluid milk. In its post-hearing brief,
NMPF maintained its opposition to
proposals that would exclude drinkable
yogurt products from the fluid milk
product definition.
Comments and exceptions filed by
NMPF in response to the Recommended
Decision opposed the exemption of kefir
and yogurt containing beverages from
the fluid milk product definition
arguing that an exemption is
inconsistent with the principle of form
and intended use. NMPF reiterated
arguments made at the hearing and in
its post-hearing brief that kefir and
yogurt containing beverages are almost
identical in form to fluid milk and are
used as beverages. NMPF purported that
data presented at the hearing by yogurt
manufacturers demonstrating that
yogurt containing beverages did not
compete with fluid milk was misleading
and the exemption would be difficult to
enforce. NMPF stated that because kefir
has no standard of identity (as does
yogurt, for example) manufacturers
could name an array of products as kefir
to avoid classification as fluid milk
products. NMPF also said the standard
of identity for yogurt was too broad and
its identity standard is currently under
review by the FDA. NMPF claimed that
exempting yogurt containing beverages
from the fluid milk product definition
could create an enormous regulatory
loophole that could be exploited to
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avoid classification of new products as
fluid milk products.
The witness appearing on behalf of
Dairy Farmers of America and Dairylea
Cooperative Inc. (DFA/DLC) also
testified in opposition to the adoption of
Proposals 8 and 9. The witness stated
that adoption of these proposals would
allow more products to be classified as
Class II products even though they
compete with fluid milk for sales. A
post-hearing brief filed by DFA/DLC
further claimed that the growth of
drinkable yogurt products in the
marketplace has not been impeded by
previous classification decisions and
that such products should not be
excluded from the fluid milk product
definition because some hearing
participants claimed it would harm the
innovation of new dairy products.
In its comments to the Recommended
Decision, Select Milk Producers, Inc.
(Select)/Continental Dairy Products
(Continental) opposed the exemption of
kefir or drinkable yogurt beverages that
contained 20 percent or more yogurt
from the fluid milk product definition.
According to their brief Select and
Continental are dairy-farmer owned
cooperatives that market milk on
various Federal orders.
The witness appearing on behalf of
Leprino testified in support of Proposal
10. The witness testified that only
products that compete with fluid milk
should be classified as fluid milk
products, therefore meal replacements
and nutritional drinks should remain
exempted from the fluid milk product
definition. In its exceptions to the
Recommended Decision Leprino
opposed the inclusion of the term
‘‘health care industry’’ in the meal
replacement exemption. Leprino argued
that this qualifier could cause a product
to hold two different classifications
depending on how it is distributed.
A post-hearing brief submitted on
behalf of Novartis stated that the
Department should exempt special
dietary need and nutritional beverages
from the fluid milk product definition.
The brief explained that Novartis’
products are not currently classified as
fluid milk products due to their
nutritional nature, the level of nonfat
milk solids contained in their product,
and because their products are only
available through foodservice and
health care channels. The brief stressed
that Novartis’ health care products were
never intended to compete with
traditional fluid milk.
The brief predicted that Novartis’
products could possibly become
reclassified as fluid milk products if a
2.25 percent protein standard were
adopted as a part of the definition. The
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brief insisted that if these products are
reclassified, it would result in higher
costs for patients with special dietary
and nutrition needs. The brief urged the
Department to exempt nutritional
products consumed for special dietary
use from the fluid milk product
definition if a protein standard was
adopted as part of the fluid milk
product definition.
A witness appearing on behalf of
Hormel testified in support of Proposal
11 seeking to exclude health care
beverages from the fluid milk product
definition. The witness testified that
fluid milk products designed for the
health care industry should be
exempted because they do not compete
with fluid milk for sales. The witness
explained that Hormel’s distribution is
primarily to health care facilities, and
they are targeted to a small segment of
the population. The witness argued that
if products designed for the health care
industry were classified as fluid milk
products, it would have no effect on
producer revenue because the products
have extremely limited distribution. The
witness explained that many products
Hormel manufactures are designed to
help counter the effects of malnutrition
in adults with a variety of medical
conditions and are not marketed nor
labeled as fluid milk. Instead, those
products are considered to be foods for
special dietary use, the witness noted,
and should be exempt from the fluid
milk product definition.
The Bravo!, et al., witness also
testified in support of the continued
exemption from the fluid milk product
definition for products such as infant
formula, meal replacements, products
packaged in hermetically sealed
containers, snack replacements, high
protein drinks, and products that
contain alcohol or are formulated for
animal use. The witness explained that
meal replacements and similar products
have historically been exempted from
the fluid milk product definition and
that their regulatory status should not be
changed.
Comments received from Bravo!, et al.
on the Recommended Decision
supported the continued exemption of
meal replacements that are sold to the
health care industry but offered a slight
modification to clarify the intent of the
exemption. Bravo!, et al., explained that
some products are considered meal
replacements and are sold both in retail
markets and through health care
professionals, health care institutions,
and weight management centers. Bravo!,
et al., asserted that a literal reading of
the Recommended Decision could lead
to one product holding two different
classifications depending on how it is
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distributed. Therefore, Bravo!, et al.,
suggested that the meal replacement
exemption be modified to read ‘‘* * *
(meal replacement) that are intended for
use in the health care industry, or
products similar in form and intended
use sold to retail customers * * *’’
The NMPF witness testified in
opposition to Proposal 10 arguing that
its adoption would eliminate important
factors in determining if a product was
specially formulated for a specific
dietary purpose that would warrant
exemption from the fluid milk product
definition. The witness was also
opposed to Proposal 11 because the
proposed language—‘‘nutrient enhanced
fortified formulas’’—was too broad and
would not clearly distinguish such
products from traditional fluid milk
products.
In its exceptions to the Recommended
Decision, NMPF opposed any
amendments to the exemption of meal
replacements from the fluid milk
product definition. NMPF stated that
the proposed use of the ‘‘health care
industry’’ distribution criteria was vague
and open-ended for interpretation on
which entities are a part of the ‘‘health
care industry.’’ NMPF was of the
opinion that the current packaging
criteria contained in the proposed meal
replacement exemption is an
appropriate guideline for what products
constitute meal replacements.
The DFA/DLC witness testified in
opposition to Proposals 10 and 11. The
witness was of the opinion that
amending the fluid milk product
definition to broaden the exemption of
products such as infant formulas and
meal replacements was not justified
because doing so would significantly
lower Class I use. This position was
reiterated in the DFA/DLC post-hearing
brief and exceptions to the
Recommended Decision. DFA, et al.,
argued that no evidence was presented
to support the removal of the packaging
criteria from the meal replacement
exemption. The exceptions asserted that
the use of packaging criteria has
historically been a way to distinguish
products that do not compete with fluid
milk because the higher cost of
hermetically sealed packaging
discouraged manufacturers from using
the exemption to circumvent Class I
pricing. DFA, et al., also took exception
to the proposed exemption of
nutritional formulas that are prepared
for the health care industry. According
to the exceptions, the types of
institutions that comprise the ‘‘health
care industry’’ are not clearly defined in
the decision. DFA, et al., asserted that
the meal replacement exemption could
cause manufacturers to sell their
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products to a health care facility for
resale in the ‘‘normal marketplace’’ to
avoid Class I pricing.
The witness appearing on behalf of
O–AT–KA testified that products
packaged in hermetically-sealed
containers or that are specialized for
longer shelf life should remain exempt
from fluid milk product classification
because those products are used as meal
replacements and meal supplements,
not as alternatives to milk. The witness
said that since the term ‘‘meal
replacement’’ is not defined in the
current definition, no change in the
exemption of hermetically sealed
containers should be made. The
position was reiterated in their brief.
The Dannon witness testified in
opposition to the adoption of Proposal
10 because it would remove the 6.5
percent nonfat milk solids standard of
the fluid milk product definition.
Exceptions to the Recommended
Decision filed by Fonterra opposed the
removal of how a product is packaged
in the infant feeding and dietary use
exemption, and the proposed
distribution to the ‘‘health care industry’’
as a method for exempting meal
replacements. Fonterra argued that
relying on how a product is distributed
could cause the same product to hold
two separate classifications. Fonterra
offered that if meal replacements are to
be exempt from fluid milk product
classification, then how a product is
distributed should not be a factor in
determining whether or not it meets the
fluid milk product definition.
Discussion and Findings
This decision provides that the fluid
milk product definition for all Federal
orders defines fluid milk products by:
(1) Continuing to provide a nonexhaustive list of named fluid milk
products; (2) Maintaining a set of
compositional standards; and (3)
Continuing to provide exceptions for
products that will be exempted from the
definition. This decision maintains the
current maximum butterfat limit of less
than nine percent for a product to still
be considered a fluid milk product. The
nonfat solids compositional standards
will consist of the current 6.5 percent
nonfat milk solids content of a product
and a true milk protein standard of 2.25
percent content of a product. The nonfat
solids standards will be applied
independently of each other. For
example, if a product contained 6
percent nonfat solids and 2.30 percent
true milk protein and less than 9
percent butterfat the product would be
considered a fluid milk product. These
standards either 6.5 percent or more
nonfat milk solids or 2.25 percent or
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more true milk protein, or less than nine
percent butterfat, will be the basis for
determining if a beverage containing
dairy ingredients meets the
compositional standards for being
defined as a fluid milk product.
The calculation of the percent true
protein and the percent nonfat milk
solids contained in a product will be
performed by measuring the true protein
and nonfat milk solids of all dairyderived ingredients contained in the
finished product. All non-fluid dairyderived ingredients used in a fluid milk
product will be classified and priced in
the same manner as nonfat dry milk (or
condensed) is currently classified and
priced when used in a fluid milk
product.
The record supports exemption of
certain drinkable products made from
milk or products containing milkderived ingredients from the fluid milk
product definition. These exemptions
include: Drinkable yogurt containing at
least 20 percent yogurt by weight and
kefir; products especially prepared for
infant feeding or dietary use as meal
replacements that are packaged in
hermetically sealed containers; and
other products that may otherwise meet
the compositional standards of a fluid
milk product but contain no fluid milk
products named in the fluid milk
product definition.
The primary goal of Federal milk
marketing orders is to establish and
maintain orderly marketing conditions.
This is achieved primarily through the
use of classified pricing (pricing milk
based on its use) and the marketwide
pooling of the proceeds of milk used in
a marketing area among all producers.
These two tools enable Federal orders to
establish minimum prices that handlers
must pay for milk based on its ultimate
use and return to producers a weighted
average or uniform price for their milk.
Through classified pricing and
marketwide pooling, Federal orders
promote and maintain orderly
marketing by equitably pricing milk
used in the same class among competing
handlers within a marketing area. This
does not mean that handlers will
necessarily have equal costs since
differences in milk tests, procurement
costs, and transportation will impact a
handler’s final raw milk costs. However,
it does allow handlers to have the same
minimum regulated price for milk used
in a particular category of products or
class of products for which they
compete for sales. The regulated
minimum price is the class price for the
respective class of use. Thus, it is
reasonable and appropriate that milk
used in identical or nearly identical
products should be placed in the same
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class of use. This tends to reduce the
incidence of disorderly marketing that
may arise because of price differences
between competing handlers.
Federal milk orders classify producer
milk as fluid milk or used to produce a
manufactured product. Producer milk
classified as Class I consists of those
products that are intended to be used as
beverages including, but not limited to,
whole milk, skim milk, low fat milk,
and flavored milk products such as
chocolate milk. Producer milk classified
as Class II includes milk used in the
production of soft or spoonable
manufactured products such as sour
cream, ice cream, cottage cheese, yogurt,
and milk that is used as ingredients in
the manufacture of other food products.
Producer milk classified as Class III
includes milk used in the production of
hard cheese products. The Class IV use
of producer milk generally consists of
milk used in the production of canned
milk, dried milk products, and butter.
Federal orders provide a definition for
‘‘fluid milk products’’ to identify the
types of products that are intended to be
consumed as beverages and to specify
that the skim milk and butterfat in these
types of milk products should be
classified as Class I and priced
accordingly. The current fluid milk
product definition contained in all
Federal milk orders provides a nonexhaustive list of products that are
specifically identified as fluid milk
products. The definition also specifies
certain compositional criteria for fluid
milk products—any product containing
less than 9 percent butterfat and 6.5
percent or more nonfat milk solids. The
definition also specifically exempts
from the fluid milk product definition
products especially prepared for infant
feeding or dietary use (meal
replacement) packaged in a
hermetically-sealed container, any
product that contains by weight less
than 6.5 percent nonfat milk solids, and
whey.
Numerous witnesses were concerned
that the definition of milk as defined by
the Food and Drug Administration
(FDA) in 21 CFR 131.110 not be
changed. A Federal milk marketing
order decision cannot change the
definition of milk. Some witnesses were
of the opinion that the addition of
various ingredients to milk would cause
the resulting product to not meet the
Grade A standard. This decision does
amend the definition of a fluid milk
product in all milk marketing orders for
the purpose of classifying producer milk
in accordance with the form in which or
the purpose for which it is used as
required by section 608(c)(5)(A) of the
Agricultural Marketing Agreement Act.
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Neither this decision nor Federal orders
in general determine if milk is Grade A
or what ingredients are allowed in milk.
Further, Federal orders do not establish
standards of identity for milk. Such
standards are established by other
agencies, such as a state board of health
or the FDA.
Testimony given at the hearing and
positions taken in post-hearing briefs
extensively discussed the importance of
form and intended use in determining
whether a product should be defined as
a fluid milk product. However,
comments to the Recommended
Decision almost universally favored the
use of specific compositional standards
rather than form and use as first
consideration which was proposed in
the Recommended Decision. These
comments have merit. Therefore as
provided in this decision, compositional
criteria will be the primary basis used
in determining whether the product is
defined as a fluid milk product.
The standards of 6.5 percent or more
nonfat milk solids or 2.25 percent or
more true milk protein are intended to
exclude from the fluid milk product
definition those products which contain
some milk solids but that are not closely
identified with the dairy industry.
The establishment of nonfat milk
solids and true milk protein standards
for classifying milk products is intended
to provide the same classification for
products having the same general form
and use. Similar products in different
classes defeat the purpose of classified
pricing and results in unequal costs
among handlers. It is not the intent of
the Federal order program to bring
products that do not resemble nor are
marketed as dairy beverages under the
fluid milk product definition. As stated
earlier, the Act requires the Secretary to
classify milk ‘‘in accordance with the
form in which or the purpose for which
it is used.’’ Currently, some products
such as re-hydrating fruit flavored sport
drinks, bottled teas, carbonated soft
drinks, or bottled water may contain
some milk-derived ingredients but they
do not resemble nor are they marketed
as dairy products.
As discussed in the comments to the
Recommended Decision, specific
compositional standards will give the
industry clearer standards from which
to determine if a product is or will be
defined as a fluid milk product,
superseding reliance on form and
intended use. When formulating new
beverage products, the industry will
have specific standards to guide product
formulation. The industry will better
know how Federal orders will
determine the prices of milk
ingredients.
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Based on record evidence,
compositional standards should
continue to be relied upon in
determining if a product meets the fluid
milk product definition. The revised
definition provides that a beverage
should contain by weight less than 9
percent butterfat and contain 6.5
percent or more nonfat milk solids or
2.25 percent or more true milk protein.
The 9 percent butterfat criterion that is
currently used as the maximum
butterfat content to differentiate
between fluid milk products and fluid
cream products (a Class II use of milk)
is unchanged. The addition of a 2.25
percent true milk protein criterion
serves to provide a sufficient basis to
distinguish whether a product is a Class
I or Class II use of milk.
Several parties filed comments in
opposition to the inclusion of the 2.25
percent true milk protein criterion. They
argued that its inclusion in the
definition is unnecessary and its
adoption may cause processors to use
non-dairy ingredients to avoid products
from being classified as a fluid milk
product.
The record of this proceeding clearly
supports the addition of a milk protein
standard to the fluid milk product
definition. The record shows that by
removing some of the lactose from milk,
a product may be produced that is in all
respects (except for the removed lactose)
identical to the form and intended use
of fluid milk products. However, using
only the 6.5 percent nonfat standard
results in this product being classified
as Class II even though its form and use
closely resembles Class I products.
Including all dairy derived
ingredients in the computation of a
product’s nonfat solids and true protein
content provides a more complete and
comprehensive basis to determine a
milk products identity as a fluid milk
product. Record evidence reveals
criticism that the current fluid milk
product definition has not changed to
reflect the technological advances in
milk processing—especially the
fractionation of milk. Such fractionation
technology has created the ability to
produce dairy-based beverages of almost
any composition, some of which are
marketed as and directly compete with
traditional fluid milk products.
Several witnesses at the hearing
addressed specific composition criterion
that should be used for determining if
a product meets the fluid milk product
definition. Proponents of the 2.25
percent true milk protein criterion
explained that with the technology to
separate the lactose from the protein in
milk, protein also should be used in
determining if a product should be a
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fluid milk product because protein is
the highest valued nonfat milk solid and
because lactose is most often not used
in the formulation of manufactured
dairy-based beverages. Under current
administrative determination of nonfat
milk solids, a dairy-based beverage with
lactose removed has generally been
determined not to be a fluid milk
product. Further, milk, in either wet or
dry form, that has lactose removed is
generalized as ‘‘milk protein concentrate
(MPC)’’ and MPC has not been
considered a nonfat milk solid. Thus,
with lactose removed, a product closely
resembling milk in form and intended
use may contain less than the current
6.5 percent nonfat milk solids even
though the protein content could exceed
the protein content of milk.
Other testimony contended that milk
protein is not a significant component
in fluid milk products and incorporating
a milk protein criterion is therefore not
appropriate. Contrary to the view that
milk protein is not a significant
component in fluid milk products, the
record of the proceeding reveals that in
whole milk, protein is the third most
abundant component following lactose
and butterfat. In lowfat milk, protein is
the second most abundant component.
Even though the record and post
hearing briefs contain considerable
discussion concerning possible new
product development and substitution
of nondairy ingredients in fluid milk
products, no evidence was presented at
the hearing to indicate at what price
level or to what degree such substitution
would take place. Testimony at the
hearing only speculated that processors
may use nondairy ingredients if the
fluid milk product definition adopted
the proposed 2.25 percent true milk
protein compositional standard.
Opponents also suggested that evidence
did not warrant any change to the fluid
milk product definition and that there
was no evidence that changing the
definition would be beneficial to dairy
farmers. Proponent witnesses argued
that adoption of a 2.25 percent true milk
protein compositional standard would
not change the classification of products
which currently do not meet the fluid
milk product definition. Neither
proponents nor opponents presented
any data to substantiate their claims of
benefit or harm to changing the fluid
milk product definition.
While the Class I use of milk is priced
on the basis of skim milk and butterfat,
skim milk and butterfat pricing do not
distinguish the components or the level
of components that are in the skim
fraction. Even if there is a greater level
of protein in the skim fraction, there is
no greater value that will be assigned to
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the skim fraction. However, producers
may benefit from products being
determined as meeting the fluid milk
product definition not because of the
adoption of the protein standard but
because the dairy ingredients in these
products are priced as Class I.
The record evidence supports that the
true milk protein or nonfat milk solids
contained in a finished product should
be used to determine if the 2.25 percent
true milk protein or the 6.5 percent
nonfat solids compositional standard
has been met. The composition of the
finished product, including all milkderived ingredients, will provide a clear
comparison of the product in question
to the products listed and defined in the
fluid milk product definition. These
ingredients include, but are not limited
to, the specific products listed in the
fluid milk definition, nonfat dry milk,
milk protein concentrate, casein,
calcium and sodium caseinate, and
whey. Although liquid whey, which is
derived from other manufacturing, may
meet the compositional standards of a
fluid milk product in its natural form,
it is not a finished product. The intent
is to specifically exclude liquid whey
from the fluid milk product definition
and account for it only when used as an
ingredient in the production of a
finished product meeting the fluid milk
product definition. The compositional
content will be computed by using the
pounds of true protein or nonfat milk
solids in the finished product. For all
other purposes, such as pricing and
pooling, the fluid equivalent of all milk
ingredients in fluid milk products,
including but not limited to nonfat dry
milk, milk protein concentrate, casein,
calcium and sodium caseinate, and
whey, will be used. The addition of a
true milk protein criterion will assist in
determining those products that should
be considered fluid milk products. The
inclusion of a true milk protein
compositional standard also will assure
that products which are comparable to
the products listed in the fluid milk
product definition are properly
classified as Class I.
Federal milk orders have consistently
been applied to provide and this
decision reaffirms that nonfat dry milk
reconstituted to make a fluid milk
product or the volume increase caused
by the use of nonfat dry milk in the
fortification of a fluid milk product
should be assessed the Class I value
because the integrity of classified
pricing is maintained and the
reconstituted or fortified product
competes with fluid uses of milk
products. Accordingly, this decision
proposes that other dairy-derived
ingredients, such as milk protein
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concentrate, casein, calcium and
sodium caseinate, and whey, that are
used or reconstituted to form a fluid
milk product or the volume increase
caused by the use of these products to
fortify a fluid milk product be priced as
Class I for the same reasons. Handlers
will be charged the current month’s
Class I price for the additional Class I
volume resulting from the use of these
ingredients in fluid milk products
contrasted to the receipt of these
products assigned to Class IV. This
reclassification charge (additional cost)
is not a separate charge but is assessed
through the increase in the handler’s
Class I utilization and is assessed
(determined) on the volume of
reconstituted milk or the volume
increase in the modified product, above
the level of an unmodified product. This
reclassification charge assures equity
between competing handlers on raw
product cost, assures producers that
they will receive the Class I value
contribution to a marketing order’s
blend price for milk marketed as a fluid
milk product, and it maintains the
integrity of classified pricing.
Based on the record, all milk-derived
ingredients, on a fluid equivalent basis,
contained in a fluid milk product will
be included in the allocation process
and the resulting classification and
pricing of producer milk. Whey, as used
herein is intended to include whey, dry
whey, and whey protein concentrates.
The fluid equivalent for those products
where the relationship between the
protein and nonfat milk solids has not
been altered will be computed using
nonfat solids, while the fluid equivalent
for those products where the
relationship between the protein and
nonfat milk solids has been altered,
such as MPCs, will be determined on a
true milk protein basis.
The methodology for computing a
handler’s cost under Federal milk orders
remains unchanged. Milk-derived
products such as nonfat dry milk, MPC,
casein, calcium and sodium caseinates
and whey will be used to determine if
the quantity of the fluid milk equivalent
in the modified fluid milk product is
greater than the volume of an
unmodified fluid milk product of the
same type and butterfat content. The
equivalent volume of the modified
product, up to the level of the volume
of an unmodified product, will be
considered Class I utilization and will
result in the inherent reclassification
charge (additional cost) in the handler’s
use value from the Class IV price to the
Class I price. Any fluid milk equivalent
in excess of this equivalent volume will
be considered a utilization of other
source milk beginning with Class IV and
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be priced accordingly. The receipt of
these milk-derived products used in a
fluid milk product will be accounted for
on a fluid equivalent basis as Class IV
other source receipts.
Comments filed in response to the
Recommended Decision, by various
parties representing producers, were in
favor of including all nonfat dairy solids
in the computation of the numerical
standards as contained in the
Recommended Decision. Their
comments reiterated the position
presented in their testimony and briefs.
Comments filed by opponents of
including all nonfat milk solids argued
that the inclusion of all nonfat solids is
unnecessary because whey and certain
other nonfat solids have not
traditionally been included in the
definition of fluid milk. They also
maintain that because no disorderly
marketing has occurred, no change is
necessary. Opponents assert that the
inclusion of all nonfat dairy solids
would capture additional products
meeting the fluid milk definition and in
turn processors would substitute
nondairy solids to avoid classification
as a fluid milk product.
As record evidence supports and as
already discussed in this decision, the
inclusion of all milk-derived ingredients
in the computation of the nonfat solids
on true protein content is appropriate.
The use of all milk-derived ingredients
used in the manufacturing of the fluid
milk product provides a more complete
basis for comparing the product to the
listed fluid milk products and a clearer
indication of the appropriate
determination of classification. In
addition, considering all milk-derived
ingredients places all current and future
products on the same set of
compositional standards.
Opponents maintain that nondairy
products will be substituted to avoid a
product being determined to be a fluid
milk product. However, opponents did
not present evidence as to the relative
prices necessary for this substitution to
occur. Opponents did not quantify any
of their claims that the recommended
decision would cause product
substitution in the manufacture of dairy
based beverages. Nor did they present
any examples of dairy ingredient
substitution. Therefore, it is virtually
impossible to determine if substitution
will occur and what the impact, if any,
may be. While there are currently
several nondairy ingredient options
available to formulate products, the
advantages of using dairy ingredients,
such as their nutrition, physical
properties, and taste, have kept dairy
ingredients as a competitive choice for
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use in the manufacture of the many new
products currently available.
Manufacturers of milk-based products
that are intended to be used for dietary
uses (meal replacements) testified that
products sold for such dietary use in
hermetically-sealed containers and the
same product sold in other types of
containers receive different regulatory
classifications. Some products, such as
those intended to be used for infant
feeding and dietary needs (meal
replacements), are currently considered
Class II products if they are
hermetically-sealed. However, the same
products in a brick-pack or other types
of packaging may be considered fluid
milk products. The record evidence
indicates that these products have a
limited distribution and in the case of
many of the dietary products, sales are
only to health care facilities (such as
hospitals and nursing homes). In
addition, these products have a very
long shelf life. The limited distribution
and packaging of these products
indicates that they do not directly
compete with Class I products. Their
intended use can be generalized as
replacements for meals by infants, the
infirm, and the elderly and not for use
as a beverage. These products as used
for medical and well-defined healthcare
applications are not fluid milk
competitors and are not of a scale, as
record evidence demonstrates, that
would cause a change in marketing
conditions for fluid milk products.
Accordingly, the term ‘‘meal
replacement’’ encompasses both those
drinkable dairy products intended to
replace meals and categorized products
intended for the health care industry,
and may include other products of
similar intended form and use.
This decision, in the narrow context
of a highly specialized and marketed
drinkable product sold to the health
care industry, continues to find that
packaging is a legitimate criterion for
considering some meal replacement
products as Class II products and others
as Class I. When dietary products (meal
replacements) are in hermetically sealed
containers such packaging confirms that
their intended use is a meal
replacement. When not so packaged,
dietary products (meal replacements)
may or may not be used to replace the
nutrition of normal meals in the health
care industry or possibly to be used in
the same manner as fluid milk. The
dietary products packaged in other than
hermetically sealed containers may or
may not have the same form and
intended use as those in hermetically
sealed containers. It is therefore not
reasonable that they should
automatically be similarly classified.
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Dietary products (meal replacements)
should be excluded from the fluid milk
product definition and should be
considered Class II products if they are
packaged in hermetically sealed
containers or if it is demonstrated
otherwise that the intended use is for
specialized health care purposes or
medically required meal substitution.
Based on the record, the products in
question have been produced to help
consumers with various dietary or
digestive problems achieve sufficient
nutritional intake through a drinkable
alternative to solid foods. These
products traditionally have added
vitamins, minerals, and proteins to
achieve a nutritional equivalent to a
‘‘typical’’ meal. In addition, these
products are packaged in hermetically
sealed containers to maintain a long
shelf life for easy handling in nursing
homes and hospitals. These products
continue to be Class II products. Similar
meal replacement products not
packaged in hermetically sealed
containers (brick packs or gable topped
containers) should be considered as
Class II products regardless of where
they are marketed if they can be shown
to be intended for the same specialized
dietary use as a product sold in a
hermetically sealed container with the
same limited use. However, fortified
milk products not intended for dietary
use (meal replacements) that are
available for a more generalized use that
would broadly compete with fluid milk
will not be exempted from the fluid
milk product definition.
Numerous comments and exceptions
were filed in response to the
Recommended Decision that are in
opposition to the elimination of
packaging and the addition of ‘‘sold to
the health care industry’’ as criteria for
excluding milk based dietary use (meal
replacement) products from the
definition of a fluid milk product. Much
of the opposition concerned the
definition of ‘‘sold to the health care
industry’’ and the application of such a
criteria. Several comments suggested
that products sold to retail stores might
be classified differently than products
sold to nursing homes or hospitals.
Based on the evidence presented in
exceptions, this decision removes the
distribution channel reference in the
fluid milk product definition to prevent
the potential dual classification of a
product.
As noted by DFA, et al., in its
exceptions to the Recommended
Decision, USDA did not receive any
proposals to change the classification of
supplements for dietary use that contain
milk-derived ingredients such as readyto-drink high protein products.
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Beverages containing milk-derived
ingredients, such as high protein drinks,
are typically packaged in hermetically
sealed containers and are currently
classified as Class II products. Such
beverages may include fruit flavored rehydrating sports drinks, bottled teas,
carbonated soft drinks and bottled
waters which may contain milk-derived
ingredients, usually in the form of whey
proteins. Because this final decision
provides for primary reliance on
compositional standards rather than on
intended form and use, products such as
these need to be specifically exempted
from the fluid milk product definition
even if they otherwise meet the
definition’s compositional standards.
Such products are clearly not the same
as other named fluid milk products of
the definition and are not used in a
manner consistent with beverage milk.
These products may often be used to
supplement nutritional needs, but are
not used or considered to be a meal
replacement. Such products, packaged
in hermetically sealed containers, will
be exempted from the fluid milk
product definition.
Exceptions to the Recommended
Decision assert that expanding
exemptions of products from the fluid
milk product definition would result in
lower producer revenue. The record of
this proceeding lacks the data to
conclude that exempting certain milkbased or milk containing products, or
reclassifying current products from one
class to another, will harm producer
revenue.
Proposal 5 called for, in part,
retaining the 6.5 percent nonfat solids
criterion and giving the Department the
flexibility to include other dairy-based
products that fell below 6.5 percent
nonfat solids as fluid milk products. At
the hearing, the proposal was modified
to require the Department to first make
other determinations and to conduct
studies before a classification
determination is made on whether the
product meets the fluid milk product
definition.
Specifically, the modified proposal
would require the Department to
determine if a product competes
directly and substantially with Food
and Drug Administration defined milk
products and also included five other
criteria the Department would have to
satisfy before a written determination of
fluid milk product classification could
be issued. The modified proposal
further required that more than three
million pounds of the product be sold
in a marketing area per month before the
product would be defined as a fluid
milk product even if the product met all
of the five criteria.
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The multi-criteria features of Proposal
5, as modified, are not consistent with
the adopted primary consideration to
compositional standards and the
requirement to classify milk on the basis
of form and intended use as provided
for in section 608(c)(5)(A) of the Act and
are not adopted. Requiring a comparison
of retail prices and advertising, and
examination of the substitutability
between the new product and already
defined fluid milk products does not
conform to the primary reliance on
compositional standards or form and
intended use in determining whether a
product meets the fluid milk product
definition. No significant improvements
to product classification determinations
would be achieved. Therefore Proposal
5 is denied.
A modification to Proposal 7 made at
the hearing is not adopted. This
modification sought to require the
Department to hold a hearing to
determine the classification of a new
product ‘‘made by new technology.’’
Such requirement is not necessary for
the same reasons in determining that
Proposal 5 and all of its modifications
are not adopted. The need to
incorporate a specific requirement to
hold a hearing is not necessary since it
is already available.
A number of opponents of proposals
seeking to change the fluid milk product
definition argued that there must
necessarily exist a current problem or
the existence of disorderly marketing
conditions before amendments to the
provisions of Federal milk marketing
orders can be made. Based on the
evidence, this decision disagrees with
such arguments. Actions to preserve the
integrity of the regulatory system have
historically been taken to avoid
problems with the goal of maintaining
orderly marketing conditions.
Amending the orders to prevent
disorderly marketing conditions from
arising is reasonable and consistent with
ensuring and maintaining orderly
conditions and equity among producers
and handlers. In light of the changing
marketing conditions, it is especially
reasonable and appropriate to provide
standards that can address both
immediate and future needs of a rapidly
changing industry brought about by new
technology.
Some witnesses testified that even if
a product meets the fluid milk product
definition, the intended use of that
product should be considered for
assigning the product to the most
appropriate class use. In this regard, if
the intended use of the product is a food
item that does not compete with
traditional fluid milk in the
marketplace, the product should be
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exempted from the fluid milk product
definition. The most notable products of
this characteristic are drinkable yogurts
that, while drinkable, are not intended
to be used as a beverage. The record
reveals that some products such as
drinkable yogurts are marketed as a food
item to supplement or even replace a
meal and intended to be used as a quick
and easy way to carry a snack. This
differentiates their intended use from
fluid milk products consumed as
beverages. The record indicates that
these products are not marketed side-byside with fluid milk products in retail
outlets. Instead, they are positioned
alongside other Class II products such as
spoonable yogurts in cups. It is
reasonable to conclude that drinkable
yogurts are yogurt in fluid form and not
flavored drinks and are sufficiently
different in intended use from other
fluid milk products to warrant their
exemption from the fluid milk product
definition.
A portion of Proposal 9 referred to
drinkable yogurt having a protein
standard of ‘‘* * * no more than 2.2
percent skim milk protein * * *’’ given
that it contained a minimum amount (20
percent) of yogurt. As just discussed
above, several witnesses testified to the
fact, and the consumer surveys and
marketplace data provided by Dannon
and General Mills explained how yogurt
containing products (e.g. drinkable
yogurt) are fundamentally different from
fluid milk. No protein standard is
adopted for drinkable yogurt because
the 20 percent yogurt content
requirement differentiates these
products and assures they are not in
competition with fluid milk.
Nevertheless, it is reasonable to
establish a minimum level of yogurt that
needs to be contained in the finished
product to differentiate them from
flavored beverages while at the same
time identifying the drinkable yogurt as
a yogurt product. No record evidence
was presented by manufacturers of
yogurt-containing beverages to
demonstrate that a 20 percent minimum
yogurt standard would cause some
yogurt beverages to be classified as fluid
milk products and others not. Therefore
based on record evidence, it is
reasonable to estimate that the current
yogurt content of these products is
above the proposed 20 percent
minimum.
Accordingly, drinkable yogurt
containing at least 20 percent yogurt by
weight should be considered a yogurt
product and as such exempt from the
fluid milk product definition. The
yogurt contained in exempted drinkable
yogurt still must meet the yogurt, lowfat yogurt, or fat-free yogurt standard of
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identity as defined by the FDA (21 CFR
131.200–131.206) and the manufacture
of the yogurt mass must be an
identifiable and quantifiable step in the
formulation process of the drinkable
yogurt.
Opponents of excluding drinkable
yogurts from the fluid milk product
definition stressed that drinkable
yogurts should not be excluded because
they are beverages and packaged
similarly to other fluid milk products.
Opponents are of the opinion that
drinkable yogurts are fluid milk
products because they are comparable to
flavored or cultured fluid milk products.
Drinkable yogurts do have several
characteristics similar to listed fluid
milk products—they can be used as a
beverage and are similarly packaged.
There are, however, other characteristics
that differentiate drinkable yogurts from
fluid milk products, as the record
indicates. These characteristics include,
in most cases, a different consistency
than the fluid milk products, a
significant volume of added yogurt, the
addition of fruit and not just flavorings,
and live and active cultures supplied by
the yogurt.
The differences between listed fluid
milk products and drinkable yogurts
warrant the exclusion of drinkable
yogurts containing at least 20 percent
yogurt from being defined as a fluid
milk product. Drinkable products with
less than 20 percent yogurt will be
considered fluid milk products. The
milk ingredients (including the yogurt
portion) contained in those products
with less than 20 percent yogurt will be
priced at the Class I price. The
Recommended Decision proposed the
yogurt portion of these Class I products
not be subject to a Class I ‘‘upcharge.’’
Fonterra’s exceptions objected to the
yogurt content not being priced as Class
I as would other milk ingredients in the
fluid milk product. Since these
beverages with less than 20 percent
yogurt will be considered a fluid milk
product, it is consistent to price the
milk ingredients in such products the
same as other Class I beverages.
Bravo!, et al., which supported
excluding drinkable yogurts from the
fluid milk product definition, proposed,
as did Lifeway Foods separately at the
hearing, to also exclude kefir. The
evidence provided to support excluding
kefir from the fluid milk product
definition identified kefir as a cultured
product similar to drinkable yogurt that,
like yogurt, contains live and active
cultures. While cultured beverages are
one of the listed products in the fluid
milk product definition, the record
shows kefir’s several similarities to
drinkable yogurts provide a reasonable
PO 00000
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basis to conclude that the milk used in
kefir products should be classified in
the same way as milk used in drinkable
yogurt products. NMPF argued that kefir
should not be exempt because no
standard of identity exists to identify
what is and is not kefir. While kefir has
no standard of identity, cultured milk
requirements are described by the U.S.
Food and Drug Administration (FDA)
(21 CFR 131.112) and kefir is
specifically listed as such a product.
Therefore, as with drinkable yogurts
containing at least 20 percent yogurt by
weight, kefir should be exempt from the
fluid milk product definition.
Producer groups were concerned
about the Recommended Decision’s
effect on producer income. The
exclusion of certain drinkable yogurts
and kefir from the fluid milk product
definition will have a minimal impact
on the resulting uniform prices to
producers. According to the record the
volume of drinkable yogurt or kefir type
beverages was less than one-half of one
percent of the packaged fluid milk
products distributed in 2004. For 2004,
it is estimated that if all of the current
drinkable yogurt and kefir beverages
had been Class II, the impact on
producers, either through the uniform
price or producer price differential,
would have been a $0.0026 per
hundredweight reduction on the more
than 103 billion pounds of producer
milk pooled on Federal orders.
NMPF argued that the form and use
of drinkable yogurt is the same as the
products listed in the fluid milk
products definition. It could be asserted
that drinkable yogurt is a beverage
similar to some of the listed fluid milk
products and it is made in this form
with the intention of people drinking
the product. However, the similarity
ends there and the record evidence
establishes numerous differences which
support drinkable yogurt and kefir to
not be treated as fluid milk products. As
pointed out in the Recommended
Decision and by proponents of both
Proposals 8 and 9 in their comments,
drinkable yogurt is marketed with
yogurt and competes with yogurt
products in the marketplace and not
with fluid milk products. As indicated
by a proponent for exempting drinkable
yogurt from the fluid milk product
definition, it is made by blending yogurt
into a liquid. This is significantly
different from flavored drinks in which
flavoring is added to a fluid milk
product. As a practical point, drinkable
yogurts do not fulfill the same intended
use as fluid milk products in the home
or commercially. For example, they are
not intended to be added to tea or
coffee, or poured on cereals, fruits and
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Federal Register / Vol. 75, No. 113 / Monday, June 14, 2010 / Proposed Rules
(a) The tentative marketing
agreements and the orders, as hereby
proposed to be amended, and all of the
terms and conditions thereof, will tend
to effectuate the declared policy of the
Act;
(b) The parity prices of milk as
determined pursuant to section 2 of the
Act are not reasonable in view of the
price of feeds, available supplies of
feeds, and other economic conditions
which affect market supply and demand
for milk in the marketing areas, and the
minimum prices specified in the
tentative marketing agreements and the
orders, as hereby proposed to be
amended, are such prices as will reflect
the aforesaid factors, insure a sufficient
quantity of pure and wholesome milk,
and be in the public interest;
(c) The tentative marketing
agreements and the orders, as hereby
proposed to be amended, will regulate
the handling of milk in the same
manner as, and will be applicable only
to persons in the respective classes of
industrial and commercial activity
specified in, marketing agreements upon
which a hearing has been held; and
(d) All milk and milk products
handled by handlers, as defined in the
tentative marketing agreements and the
orders as hereby proposed to be
amended, are in the current of interstate
commerce or directly burden, obstruct,
or affect interstate commerce in milk or
its products.
Rulings on Proposed Findings and
Conclusions
Briefs, proposed findings and
conclusions were filed on behalf of
certain interested parties. These briefs,
proposed findings and conclusions, and
the evidence in the record were
considered in making the findings and
conclusions set forth above. To the
extent that the suggested findings and
conclusions filed by interested parties
are inconsistent with the findings and
conclusions set forth herein, the
requests to make such findings or reach
such conclusions are denied for the
reasons previously stated in this
decision.
wwoods2 on DSK1DXX6B1PROD with PROPOSALS_PART 1
other foods, and to be consumed as a
beverage.
NMPF, in their exceptions to the
Recommended Decision, pointed out
that the FDA may change the standard
of identity of yogurt and therefore it is
inappropriate to use the current FDA
standard of identity as a criterion in
determining that drinkable yogurt
which contains more than 20 percent
yogurt is not a fluid milk product.
NMPF exceptions also opposed the
exemption of kefir from the fluid milk
product definition for many of the same
reasons for exempting drinkable yogurt.
As NMPF correctly notes, kefir is a
cultured fermented beverage. A cultured
fermented beverage such as kefir is
equally dissimilar to the other listed
fluid milk products as these described
drinkable yogurts.
After careful review and
consideration of the record evidence
and the reasons as stated above, this
decision concludes that drinkable
yogurt containing at least 20 percent
yogurt by weight, and kefir should not
be defined as fluid milk products. As
such, this determination represents the
adoption of Proposal 8, the requirement
that drinkable yogurt products contain
at least 20 percent yogurt by weight to
be excluded from the fluid milk product
definition as included in Proposal 9,
and the proposal of Bravo!, et al., as
well as Lifeway Foods that kefir be
exempt from the fluid milk product
definition. Milk used to produce these
products will be classified as a Class II
use of milk.
In arriving at the findings and
conclusions, and the regulatory
provisions of this decision, each of the
exceptions received was carefully and
fully considered in conjunction with the
record evidence. To the extent that the
findings and conclusions and the
regulatory provisions of this decision
are at variance with any of the
exceptions, such exceptions are hereby
overruled for the reasons previously
stated in this decision.
General Findings
The findings and determinations
hereinafter set forth supplement those
that were made when the Northeast and
other marketing orders were first issued
and when they were amended. The
previous findings and determinations
are hereby ratified and confirmed,
except where they may conflict with
those set forth herein.
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Rulings on Exceptions
Marketing Agreement and Order
Annexed hereto and made a part
hereof are two documents: A Marketing
Agreement regulating the handling of
milk, and an Order amending the orders
regulating the handling of milk in the
Northeast and other marketing areas,
which has been decided upon as the
detailed and appropriate means of
effectuating the foregoing conclusions.
It is hereby ordered that this entire
decision and the two documents
annexed hereto be published in the
Federal Register.
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33551
Referendum Order To Determine
Producer Approval; Determination of
Representative Period; and Designation
of Referendum Agent
It is hereby directed that a referenda
be conducted and completed on or
before the 30th day from the date this
decision is published in the Federal
Register, in accordance with the
procedures for the conduct of referenda
[7 CFR 900.300–311], to determine
whether the issuance of the orders as
amended and hereby proposed to be
amended, regulating the handling of
milk in the Northeast, Appalachian,
Florida, Southeast, Upper Midwest,
Central, Mideast, Pacific Northwest,
Southwest and Arizona marketing areas
is approved or favored by producers, as
defined under the terms of the order, as
amended and as hereby proposed to be
amended, who during such
representative period were engaged in
the production of milk for sale within
the aforesaid marketing areas.
The representative period for the
conduct of such referenda is hereby
determined to be June 2009.
The agents of the Secretary of
Agriculture to conduct such referenda
are hereby designated to be the
respective market administrators of the
aforesaid orders.
List of Subjects in 7 CFR Part 1000
Milk marketing orders.
Order Amending the Orders Regulating
the Handling of Milk in the Northeast
and Other Marketing Areas
This order shall not become effective
until the requirements of § 900.14 of the
rules of practice and procedure
governing proceedings to formulate
marketing agreements and marketing
orders have been met.
Findings and Determinations
The findings and determinations
hereinafter set forth supplement those
that were made when the orders were
first issued and when they were
amended. The previous findings and
determinations are hereby ratified and
confirmed, except where they may
conflict with those set forth herein.
(a) Findings. A public hearing was
held upon certain proposed
amendments to the tentative marketing
agreements and to the orders regulating
the handling of milk in the Northeast
and other marketing areas. The hearing
was held pursuant to the provisions of
the Agricultural Marketing Agreement
Act of 1937, as amended (7 U.S.C. 601–
674), and the applicable rules of
practice and procedure (7 CFR part 900).
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33552
Federal Register / Vol. 75, No. 113 / Monday, June 14, 2010 / Proposed Rules
Upon the basis of the evidence
introduced at such hearing and the
record thereof, it is found that:
(1) The said orders as hereby
amended, and all of the terms and
conditions thereof, will tend to
effectuate the declared policy of the Act;
(2) The parity prices of milk, as
determined pursuant to Section 2 of the
Act, are not reasonable in view of the
price of feeds, available supplies of
feeds, and other economic conditions
which affect market supply and demand
for milk in the aforesaid marketing
areas. The minimum prices specified in
the orders as hereby amended are such
prices as will reflect the aforesaid
factors, insure a sufficient quantity of
pure and wholesome milk, and be in the
public interest;
(3) The said orders as hereby
amended regulate the handling of milk
in the same manner as, and are
applicable only to persons in the
respective classes of industrial or
commercial activity specified in, a
marketing agreement upon which a
hearing has been held; and
(4) All milk and milk products
handled by handlers, as defined in the
marketing agreements and the orders as
hereby amended, are in the current of
interstate commerce in milk or its
products.
Order Relative to Handling
It is therefore ordered, that on and
after the effective date hereof, the
handling of milk in the Northeast and
other marketing areas shall be in
conformity to and in compliance with
the terms and conditions of the order, as
amended, and as hereby amended, as
follows:
For the reasons set forth in the
preamble, 7 CFR part 1000 is proposed
to be amended as follows:
PART 1000—GENERAL PROVISIONS
OF FEDERAL MILK MARKETING
ORDERS
1. The authority citation for 7 CFR
Part 1000 continues to read as follows:
Authority: 7 U.S.C. 601–674, and 7253.
wwoods2 on DSK1DXX6B1PROD with PROPOSALS_PART 1
2. In § 1000.15 paragraphs (a) and
(b)(1) are revised to read as follows:
§ 1000.15
Fluid milk product.
(a) Except as provided in paragraph
(b) of this section, fluid milk product
shall mean any milk products in fluid
or frozen form that are intended to be
used as beverages containing less than
9 percent butterfat and 6.5 percent or
more nonfat solids or 2.25 percent or
more true milk protein. Sources of such
nonfat solids/protein include but are not
limited to: Casein, whey protein
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14:20 Jun 11, 2010
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concentrate, milk protein concentrate,
dry whey, caseinates, lactose, and any
similar dairy derived ingredient. Such
products include, but are not limited to:
Milk, fat-free milk, lowfat milk, light
milk, reduced fat milk, milk drinks,
eggnog and cultured buttermilk,
including any such beverage products
that are flavored, cultured, modified
with added or reduced nonfat solids,
sterilized, concentrated, or
reconstituted. As used in this part, the
term concentrated milk means milk that
contains not less than 25.5 percent, and
not more than 50 percent, total milk
solids.
(b) * * *
(1) Any product that contains less
than 6.5 percent nonfat milk solids or
contains less than 2.25 percent true milk
protein; whey; plain or sweetened
evaporated milk/skim milk; sweetened
condensed milk/skim milk; yogurt
containing beverages with 20 or more
percent yogurt by weight and kefir;
products especially prepared for infant
feeding or dietary use (meal
replacement) that are packaged in
hermetically sealed containers; and
products that meet the compositional
standards specified in paragraph (a) of
this section but contain no fluid milk
products included in paragraph (a) of
this section.
*
*
*
*
*
3. In § 1000.40 paragraphs (b)(2)(iii)
and (b)(2)(vi) are revised to read as
follows:
§ 1000.40
Classes of utilization.
*
*
*
*
*
(b) * * *
(2) * * *
(iii) Aerated cream, frozen cream, sour
cream, sour half-and-half, sour cream
mixtures containing nonmilk items;
yogurt, including yogurt containing
beverages with 20 percent or more
yogurt by weight and kefir, and any
other semi-solid product resembling a
Class II product;
*
*
*
*
*
(vi) Products especially prepared for
infant feeding or dietary use (meal
replacements) that are packaged in
hermetically sealed containers and
products that meet the compositional
standards of § 1000.15(a) but contain no
fluid milk products included in
§ 1000.15(a);
*
*
*
*
*
4. In § 1000.43 paragraph (c) is revised
to read as follows:
§ 1000.43
General classification rules.
*
*
*
*
*
(c) If any of the water but none of the
nonfat solids contained in the milk from
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Fmt 4702
Sfmt 4702
which a product is made is removed
before the product is utilized or
disposed of by the handler, the pounds
of skim milk in such product that are to
be considered under this part as used or
disposed of by the handler shall be an
amount equivalent to the nonfat milk
solids contained in such product plus
all of the water originally associated
with such solids. If any of the nonfat
solids contained in the milk from which
a product is made are removed before
the product is utilized or disposed of by
the handler, the pounds of skim milk in
such product that are to be considered
under this part as used or disposed of
by the handler shall be an amount
equivalent to the nonfat milk solids
contained in such product plus all of
the water and nonfat solids originally
associated with such solids determined
on a protein equivalent basis.
*
*
*
*
*
Note: The following will not appear in the
Code of Federal Regulations.
Marketing Agreement Regulating the
Handling of Milk in Certain Marketing
Areas
The parties hereto, in order to
effectuate the declared policy of the Act,
and in accordance with the rules of
practice and procedure effective
thereunder (7 CFR part 900), desire to
enter into this marketing agreement and
do hereby agree that the provisions
referred to in paragraph I hereof, as
augmented by the provisions specified
in paragraph II hereof, shall be and are
the provisions of this marketing
agreement as if set out in full herein.
I. The findings and determinations,
order relative to handling, and the
provisions of § lll to lll 1 all
inclusive, of the order regulating the
handling of milk in the llllll 2
marketing area (7 CFR part lll 3);
and
II. The following provisions:
§ llllll 4 Record of milk handled
and authorization to correct
typographical errors.
(a) Record of milk handled. The
undersigned certifies that he/she
handled during the month of
lllll 5, lllll hundredweight
of milk covered by this marketing
agreement.
(b) Authorization to correct
typographical errors. The undersigned
hereby authorizes the Deputy
Administrator, or Acting Deputy
1 First
and last section of order.
of order.
3 Appropriate part number.
4 Next consecutive section number.
5 Appropriate representative period for the order.
2 Name
E:\FR\FM\14JNP1.SGM
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Federal Register / Vol. 75, No. 113 / Monday, June 14, 2010 / Proposed Rules
DEPARTMENT OF TRANSPORTATION
with installation of the Mid-Continent
Instruments MD835 Lithium Ion (Li-ion)
battery. The applicable airworthiness
regulations do not contain adequate or
appropriate safety standards for this
design feature. These proposed special
conditions contain the additional safety
standards that the Administrator
considers necessary to establish a level
of safety equivalent to that established
by the existing airworthiness standards.
DATES: We must receive your comments
by July 14, 2010.
ADDRESSES: Mail two copies of your
comments to: Federal Aviation
Administration, Regional Counsel,
ACE–7, 901 Locust, Room 506, Kansas
City, Missouri 64106. You may deliver
two copies to the Small Airplane
Directorate at the above address. Mark
your comments: Docket No. CE307. You
may inspect comments in the Rules
Docket weekdays, except Federal
holidays, between 7:30 a.m. and 4 p.m.
FOR FURTHER INFORMATION CONTACT:
James Brady, Regulations and Policy
Branch, ACE–111, Federal Aviation
Administration, Small Airplane
Directorate, Aircraft Certification
Service, 901 Locust, Kansas City, MO
64106; telephone (816) 329–4132;
facsimile (816) 329–4090.
SUPPLEMENTARY INFORMATION:
Federal Aviation Administration
Comments Invited
Administrator, Dairy Programs,
Agricultural Marketing Service, to
correct any typographical errors which
may have been made in this marketing
agreement.
Effective date. This marketing
agreement shall become effective upon
the execution of a counterpart hereof by
the Department in accordance with
Section 900.14(a) of the aforesaid rules
of practice and procedure.
In Witness Whereof, The contracting
handlers, acting under the provisions of
the Act, for the purposes and subject to
the limitations herein contained and not
otherwise, have hereunto set their
respective hands and seals.
Signature
By (Name) lllllllllllll
(Title) lllllllllllllll
(Address)
lllllllllllll
(Seal)
Attest lllllllllllllll
Dated: May 21, 2010.
Rayne Pegg,
Administrator, Agricultural Marketing
Service.
[FR Doc. 2010–12771 Filed 6–11–10; 8:45 am]
BILLING CODE P
14 CFR Part 23
[Docket No. CE307; Notice No. 23–10–01–
SC]
Special Conditions: AeroMech,
Incorporated; Hawker Beechcraft
Corporation, Model B200 and Other
Aircraft Listed in Table 1, Approved
Model List (AML); Installation of MD835
Lithium Ion Battery
wwoods2 on DSK1DXX6B1PROD with PROPOSALS_PART 1
AGENCY: Federal Aviation
Administration (FAA), DOT.
ACTION: Notice of proposed special
conditions.
SUMMARY: This action proposes special
conditions for the AeroMech,
Incorporated; Hawker Beechcraft
Corporation, model B200 and other part
23 aircraft listed on the AML. These
airplanes as modified by AeroMech,
Incorporated will have a novel or
unusual design feature(s) associated
We invite interested persons to
submit written data, views, or
arguments as they desire. The most
helpful comments reference a specific
portion of the special conditions,
explain the reason for any
recommended change, and include
supporting data. We ask that you send
us two copies of written comments.
We will file in the docket all
comments we receive, as well as a
report summarizing each substantive
public contact with FAA personnel
concerning these special conditions.
You may inspect the docket before and
after the comment closing date. If you
wish to review the docket in person, go
to the address in the ADDRESSES section
of this preamble between 7:30 a.m. and
4 p.m., Monday through Friday, except
Federal holidays.
We will consider all comments we
receive on or before the closing date for
comments. We will consider comments
33553
filed late if it is possible to do so
without incurring expense or delay. We
may change these special conditions
based on the comments we receive.
If you want the FAA to acknowledge
receipt of your comments on this
proposal, include with your comments
a pre-addressed, stamped postcard on
which the docket number appears. We
will stamp the date on the postcard and
mail it back to you.
Background
On September 18, 2009, AeroMech,
Incorporated applied for a supplemental
type certificate AML for installation of
the Mid-Continent Instruments MD835
Li-ion battery in the Hawker Beechcraft
Corporation, B200 and other aircraft
listed on the AML. The AML covers part
23 aircraft that currently use the PS–835
lead-acid emergency battery.
The current regulatory requirements
for part 23 airplanes do not contain
adequate requirements for the
application of Li-ion batteries in
airborne applications. AeroMech,
Incorporated proposes to replace an
existing L–3 Communications PS–835
lead-acid emergency battery with a MidContinent Instruments MD835 Li-ion
battery on part 23 aircraft currently
equipped with the PS–835 battery. This
type of battery possesses certain failure,
operational, and maintenance
characteristics that differ significantly
from that of the nickel cadmium (Ni-Cd)
and lead-acid rechargeable batteries
currently approved in other normal,
utility, acrobatic, and commuter
category airplanes.
Type Certification Basis
Under the provisions of § 21.101,
AeroMech, Incorporated must show that
the Hawker Beechcraft Corporation
B200 and other aircraft listed on the
AML continue to meet the applicable
provisions of the regulations
incorporated by reference in the type
certificate of each model listed and the
applicable regulations in effect on the
date of application for the change. The
regulations incorporated by reference in
the type certificate are commonly
referred to as the ‘‘original type
certification basis.’’ The certification
basis for each model qualified for this
modification is detailed below.
TABLE 1—APPROVED MODEL LIST
Aircraft make
Aircraft model
TCDS
Certification basis for alteration
Aero Vodochody ..........
Ae 270 .............................................................
A58CE Rev 3 .............
Cessna ........................
441 ..................................................................
A28CE ........................
14 CFR part 23 amdt 23–59, except for 14
CFR 23.1308.
14 CFR part 23 amdt 23–59, except for 14
CFR 23.1308.
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Agencies
[Federal Register Volume 75, Number 113 (Monday, June 14, 2010)]
[Proposed Rules]
[Pages 33534-33553]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-12771]
========================================================================
Proposed Rules
Federal Register
________________________________________________________________________
This section of the FEDERAL REGISTER contains notices to the public of
the proposed issuance of rules and regulations. The purpose of these
notices is to give interested persons an opportunity to participate in
the rule making prior to the adoption of the final rules.
========================================================================
Federal Register / Vol. 75, No. 113 / Monday, June 14, 2010 /
Proposed Rules
[[Page 33534]]
DEPARTMENT OF AGRICULTURE
Agricultural Marketing Service
7 CFR Part 1000
[Doc. No. AMS-DA-09-0062; AO-14-A73, et al.; DA-03-10]
Milk in the Northeast and Other Marketing Areas; Final Decision
on Proposed Amendments to Marketing Agreements and Orders
AGENCY: Agricultural Marketing Service, USDA.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This final decision maintains the current fluid milk product
definition's compositional standard of 6.5 percent nonfat milk solids
criterion and incorporates an equivalent 2.25 percent true milk protein
criterion for determining if a product meets the compositional
standard. The decision also determines how milk and milk-derived
ingredients should be priced under all Federal milk marketing orders
when used in products meeting the fluid milk product definition. The
decision provides exemptions for drinkable yogurt products containing
at least 20 percent yogurt (by weight), kefir, and products intended to
be meal replacements from the fluid milk product definition. The orders
as amended are subject to producer approval by referendum before they
can be implemented.
FOR FURTHER INFORMATION CONTACT: Henry H. Schaefer, Economist, USDA/
AMS/Dairy Programs, Upper Midwest Milk Market Administrators Office,
Suite 200, 1600 West 82nd Street, Minneapolis, Minnesota 55431-1420,
(952) 831-5292, e-mail address: hschaefer@fmma30.com; or William
Francis, Associate Deputy Administrator, USDA/AMS/Dairy Programs, Order
Formulation and Enforcement, Stop 0231-Room 2971-S, 1400 Independence
Avenue, SW., Washington, DC 20250-0231, (202) 720-6274, e-mail address:
william.francis@ams.usda.gov.
SUPPLEMENTARY INFORMATION: This final decision maintains the current
fluid milk product definition's compositional standard of 6.5 percent
nonfat milk solids and incorporates an equivalent 2.25 percent true
milk protein criterion for determining if a product meets the
compositional standard. The decision also determines how milk and milk-
derived ingredients should be priced under all Federal milk marketing
orders when used in products meeting the fluid milk product definition.
The decision exempts drinkable yogurt products containing at least 20
percent yogurt (by weight), kefir, infant formulas, dietary products
(meal replacements) and other products that may contain milk-derived
ingredients from the fluid milk product definition.
This administrative action is governed by the provisions of
Sections 556 and 557 of Title 5 of the United States Code and,
therefore, is excluded from the requirements of Executive Order 12866.
The proposed amendments to the rules herein have been reviewed under
Executive Order 12988, Civil Justice Reform. They are not intended to
have a retroactive effect. The Agricultural Marketing Agreement Act of
1937 (Act), as amended (7 U.S.C. 604-674), provides that administrative
proceedings must be exhausted before parties may file suit in court.
Under Section 608c(15)(A) of the Act, any handler subject to an order
may request modification or exemption from such order by filing with
the Department a petition stating that the order, any provision of the
order, or any obligation imposed in connection with the order is not in
accordance with the law. A handler is afforded the opportunity for a
hearing on the petition. After a hearing, the Department would rule on
the petition. The Act provides that the district court of the United
States in any district in which the handler is a habitant, or has its
principal place of business, has jurisdiction in equity to review the
USDA's ruling on the petition, provided a bill in equity is filed not
later than 20 days after the date of the entry of the ruling.
Regulatory Flexibility Act and Paperwork Reduction Act
In accordance with the Regulatory Flexibility Act (5 U.S.C. 601 et
seq.), the Agricultural Marketing Service has considered the economic
impact of this action on small entities and has certified that this
proposed rule will not have a significant economic impact on a
substantial number of small entities. For the purpose of the Regulatory
Flexibility Act, a dairy farm is considered a ``small business'' if it
has an annual gross revenue of less than $750,000, and a dairy products
manufacturer is a ``small business'' if it has fewer than 500
employees.
For the purposes of determining which dairy farms are ``small
businesses,'' the $750,000 per year criterion was used to establish a
production guideline of 500,000 pounds per month. Although this
guideline does not factor in additional monies that may be received by
dairy producers, it should be an inclusive standard for most ``small''
dairy farmers. For purposes of determining a handler's size, if the
plant is part of a larger company operating multiple plants that
collectively exceed the 500-employee limit, the plant will be
considered a large business even if the local plant has fewer than 500
employees.
For the month of June 2005, the month the hearing was held, 52,425
dairy farmers were pooled on the Federal order system. Of the total,
49,160, or 94 percent were considered small businesses. During the same
month, 1,530 plants were regulated by or reported their milk receipts
to their respective Market Administrator. Of the total, 847, or 55
percent were considered small businesses.
The fluid milk product definition sets out the criteria for
determining if the use of producer milk and milk-derived ingredients in
such products should be priced at the Class I price. The established
criteria for the classification of producer milk are applied in an
identical fashion to both large and small businesses and will not have
any different impact on those businesses producing fluid milk products
thus assuring that similarly situated handlers have the same minimum
price as required by Section 608(c)5 of the Act. Therefore, the
amendments will not have a significant economic impact on a substantial
number of small entities. The impact of the proposed amendments on
large and small entities would be negligible. In fact, the amendment
proposing to change the
[[Page 33535]]
classification of kefir and drinkable yogurt is estimated to affect
blend prices by no more than $ 0.0026 per cwt based on record evidence.
The Agricultural Marketing Service is committed to complying with
the E-Government Act to promote the use of the Internet and other
information technologies to provide increased opportunities for citizen
access to Government information and services, and for other purposes.
A review of reporting requirements was completed under the
Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). It was
determined that these amendments would have no impact on reporting,
recordkeeping, or other compliance requirements because they would
remain identical to the current requirements. No new forms are proposed
and no additional reporting requirements are necessary.
This notice does not require additional information collection that
needs clearance by the Office of Management and Budget (OMB) beyond
currently approved information collection. The primary sources of data
used to complete the forms are routinely used in most business
transactions. The forms require only a minimal amount of information
that can be supplied without data processing equipment or a trained
statistical staff. Thus, the information collection and reporting
burden is relatively small. Requiring the same reports for all handlers
does not significantly disadvantage any handler that is smaller than
the industry average.
Prior Documents in This Proceeding
Notice of Hearing: Issued April 6, 2005; published April 12, 2005
(70 FR 19012).
Recommended Decision: Issued May 12, 2006; published May 17, 2006
(71 FR 28590).
Preliminary Statement
Notice is hereby given of the filing with the Hearing Clerk of this
final decision with respect to the proposed amendments to the marketing
agreements and the orders regulating the handling of milk in the
Northeast and other marketing areas. This notice is issued pursuant to
the provisions of the Agricultural Marketing Agreement Act and
applicable rules of practice and procedure governing the formulation of
marketing agreements and marketing orders (7 CFR Part 900).
A public hearing was held upon proposed amendments to the marketing
agreements and the orders regulating the handling of milk in all
Federal milk marketing areas. The hearing was held pursuant to the
provisions of the Agricultural Marketing Agreement Act of 1937 (AMAA),
as amended (7 U.S.C. 601-674), and the applicable rules of practice and
procedure governing the formulation of marketing agreements and
marketing orders (7 CFR Part 900).
The proposed amendments set forth below are based on the record of
a public hearing held in Pittsburgh, Pennsylvania, on June 20-23, 2005,
pursuant to a notice of hearing issued April 6, 2005 and published
April 12, 2005 (70 FR 19012); and a recommended decision issued May 12,
2006 and published May 17, 2006 (71 FR 28590).
The material issues on the record of the hearing relate to:
1. Amending the fluid milk product definition.
Findings and Conclusions
This final decision maintains the current fluid milk product
definition's compositional standard of 6.5 percent nonfat milk solids
and incorporates an equivalent 2.25 percent true milk protein criterion
for determining whether a product meets the compositional standard. The
decision also determines how milk and milk-derived ingredients should
be priced under all orders when used in products meeting the fluid milk
product definition. The decision exempts drinkable yogurt products
containing at least 20 percent yogurt (by weight), kefir, infant
formulas, dietary products (meal replacements) and other products that
may contain milk-derived ingredients from the fluid milk product
definition.
All Federal milk orders currently state that ``fluid milk product
means any milk products in fluid or frozen form containing less than 9
percent butterfat that are intended to be used as beverages.'' The
fluid milk product definition also contains a non-definitive list of
dairy products that are named fluid milk products. In addition to the
compositional butterfat standard fluid milk products shall not include,
among other products, ``* * * any product that contains by weight less
than 6.5 percent nonfat milk solids * * *'' Dairy products that do not
fall within these limits are not considered fluid milk products and the
milk used to produce these products is classified in Class II, Class
III or Class IV, depending on the form or purpose for which the
products are to be used.
Eleven proposals were published in the hearing notice for this
proceeding. Proposals 1, 3, 4 and 6 were abandoned at the hearing by
their proponents in support of other noticed proposals. No further
reference to these proposals will be made.
A proposal published in the hearing notice as Proposal 2, offered
by Dairy Farmers of America, Inc. (DFA), seeks to amend the fluid milk
product definition to include any dairy ingredient, including whey,
when calculating the milk contained in a product on a protein-
equivalent or nonfat solids equivalent basis. DFA is a dairy farmer-
member owned cooperative and at the time of the hearing had 12,800
member farms located in 49 states whose members' milk is pooled
throughout the Federal order system.
H.P. Hood LLC (H.P. Hood) owns and operates milk processing and
manufacturing plants in the Eastern and Midwest United States and is
the proponent of a proposal published in the hearing notice as Proposal
5 that was modified at the hearing. As modified, Proposal 5 seeks to
amend the fluid milk product definition to include any product that,
based upon substantial evidence as determined by the Department,
directly competes with other fluid milk products and that the
Department must make a written determination before any product can be
classified as a fluid milk product.
A proposal published in the hearing notice as Proposal 7 was
offered by the National Milk Producers Federation (NMPF). At the time
of the hearing NMPF consisted of 33 dairy-farmer member cooperatives
that represented more than 75 percent of U.S. dairy farmers. Proposal 7
seeks to amend the fluid milk product definition by removing the
reference ``6.5 percent nonfat solids standard and whey,'' and adopting
a 2.25 percent true milk protein criterion. During the hearing, DFA
offered a modification to Proposal 7 by seeking to authorize the
Department to make an interim classification determination for new
products that result from new technology. The Department would then
convene a hearing to address the use of the new technology in
classification decisions and make a final classification determination
for the new product within one year.
Proposal 8 seeks to amend the fluid milk product definition by
excluding yogurt-containing beverages from the fluid milk product
definition. This proposal was offered by The Dannon Company, Inc.
(Dannon), a wholly owned subsidiary of The Danone Group that produces
yogurt and fresh dairy products in 40 countries, including the United
States.
Proposal 9 also seeks to amend the fluid milk product definition by
excluding drinkable food products with
[[Page 33536]]
no more than 2.2 percent skim milk protein provided the product
contains at least 20 percent yogurt (nonfat yogurt, lowfat yogurt or
yogurt) by weight from the fluid milk product definition. Proposal 9
was offered by General Mills, Inc. (General Mills), a food manufacturer
that markets such products as Yoplait yogurt and yogurt-containing
products in over 100 countries, including the United States.
A proposal published in the hearing notice as Proposal 10 was
offered by the Novartis Nutrition Corporation (Novartis). Novartis
develops and manufactures a variety of products, including milk-based
products, designed to meet specific nutritional needs. Proposal 10
seeks to amend the fluid milk product definition by excluding formulas
prepared for dietary use by removing the words ``(meal replacement)
that are packaged in hermetically-sealed containers.'' The proposal
would remove the 6.5 percent nonfat milk solids standard.
A proposal published in the hearing notice as Proposal 11 seeks to
amend the fluid milk product definition by excluding health care
beverages distributed to the health care industry. Proposal 11 was
offered by Hormel Foods, LLC (Hormel), a wholly owned subsidiary of
Hormel Foods Corporation and manufacturer of a variety of food products
primarily for the health care industry.
A witness appearing on behalf of NMPF testified in support of
Proposal 7. The witness testified that Proposal 7 would close loopholes
in the current fluid milk product definition that have allowed products
developed as a result of new technology to avoid classification as
fluid milk products. The witness said that the 6.5 percent nonfat
solids standard should be eliminated and replaced with a 2.25 percent
protein standard that would also include whey proteins in determining
if the product meets the protein standard. The witness stressed that
whey proteins should be specifically defined as whey proteins that are
a by-product of the cheese making process. The witness was of the
opinion that adoption of Proposal 7 would not alter the classification
of any product currently being marketed.
The NMPF witness stressed that Federal order regulations have
always adapted to marketing conditions and that the current fluid milk
product definition should be amended to reflect changes in market
conditions brought about by changes in technology. The witness
testified that technology has evolved such that milk can now be
separated into numerous components that can be recombined to create a
vast number of new milk products. The witness argued that new
technology has enabled manufacturers to manipulate milk components,
such as removing lactose or substituting whey for other milk solids, to
create new products that contain less than 6.5 percent nonfat milk
solids. This enables manufacturers of the new products to avoid
classification of the new product as a fluid milk product even though
the form and use does not differ from what is currently considered a
fluid milk product.
The NMPF witness testified that Carb Countdown[supreg], a product
manufactured by the H.P. Hood Company, contains whey and has a reduced
lactose content that results in its composition being below the 6.5
percent nonfat milk solids standard. According to the witness, two
market research studies suggest that the product is similar in form and
use to traditional fluid milk. Relying upon a market study conducted by
IRI, a market research firm, the witness related that 98.4 percent of
Carb Countdown[supreg] sales are purchased as a substitute for fluid
milk while only 1 percent of its sales are represented as an expansion
of the fluid milk market.
The NMPF witness was of the opinion that classifying a product on
the basis of protein is appropriate because protein is the highest
valued skim component in the marketplace. The witness testified that a
2.25 percent protein standard is the appropriate equivalent of the
current 6.5 percent nonfat milk solids standard. The witness asserted
that protein has the most value to producers, processors and consumers
because it contributes nutrition, flavor and texture to milk. While the
witness was of the opinion that all dairy-derived ingredients should be
used in computing the true protein standard of a product, the witness
did not believe whey and whey product ingredients should be priced at
the Class I price. The witness maintained that the use of whey and whey
products should not exclude a product from the fluid milk product
definition because manufacturers are using whey in their new products
to avoid a fluid milk product classification. The witness also noted
that instead of relying upon the Food and Drug Administration (FDA)
standard, the Department should provide its own definition of whey.
A post-hearing brief submitted on behalf of NMPF reiterated the
positions testified to at the hearing. The brief asserted that adoption
of a milk protein standard would close regulatory loopholes that
prevent products developed as a result of new technology from avoiding
classification as a fluid milk product. According to the brief,
adoption of a true protein standard merely changes the way milk
proteins are accounted for and would not change the classification of
any product. However, these changes would capture those products
currently formulated to avoid being classified as fluid milk products.
Comments and exceptions to the Recommended Decision filed by NMPF
supported the proposed adoption of the 2.25 percent milk protein
standard, the inclusion of all nonfat milk ingredients in determining a
product's composition, and the Class I pricing of milk protein
concentrates (MPCs) used in fluid milk products. NMPF strongly opposed
exemption of casein and caseinates used in fluid milk products from
Class I pricing. They view such exemptions as differential treatment
that could cause market disorder and provide incentives for
manufacturers to use these un-priced ingredients in their fluid milk
products. NMPF was of the opinion that casein and caseinates are not
substantially different than MPCs to justify a different pricing
treatment when used in fluid milk products. However, NMPF maintained
that only whey resulting from the production of cheese should be
exempted from Class I pricing when used as an ingredient in fluid milk
products.
NMPF comments and exceptions asserted that manufacturers have
historically relied on the quantitative composition standards contained
in the fluid milk product definition when making decisions regarding
new product development. NMPF expressed opposition to the proposed
reference to ``form and intended use'' in the fluid milk product
definition because, in NMPF's opinion, it could cause manufacturers to
decrease their use of dairy ingredients in order to prevent a product
from being classified and priced as a fluid milk product. NMPF urged
abandoning the ``form and intended use'' standard and relying solely on
the protein and nonfat solids compositional standards in making
classification decisions.
A witness from DFA, appearing on behalf of DFA and Dairylea
Cooperative, Inc., (DLC), testified in support of NMPF's Proposal 7 and
Proposal 2. DLC is a dairy farmer-member owned cooperative with 2,400
member farms located in 7 states at the time of the hearing.
The DFA/DLC witness was of the opinion that the purpose of the
hearing was to refine the fluid milk product definition to reflect
current market conditions brought about by technological innovations to
ensure that
[[Page 33537]]
dairy farmers are equitably paid for their milk. The witness testified
that dairy processing technology, such as ultra filtration and milk
component fractionalization, has enabled new products to be developed
that were not foreseen when the current classification definition was
last considered.
The DFA/DLC witness testified that the current fluid milk product
definition does not recognize the value of dairy proteins in the
development of new products and therefore does not classify and
subsequently price these new products appropriately. The witness
claimed that manufacturers formulate their products to contain less
than 6.5 percent total nonfat milk solids to avoid a Class I use of
milk classification even though these products compete directly with
and are substitutes for fluid milk.
The DFA/DLC witness was of the opinion that the form and use of a
product should be the primary factor in determining product
classification. The witness said that secondary criteria used to make
classification determinations should include such factors as product
composition, a specific but not exclusive list of included and excluded
dairy products, product substitutability and enhancement of producer
revenue. The witness argued that eliminating the current total nonfat
milk solids standard and replacing it with an equivalent milk protein
standard would better reflect the demand for dairy proteins in the
marketplace.
The DFA/DLC witness offered a modification to Proposal 7 that the
witness said would provide the Department with latitude for classifying
future products that are a result of new technology. The witness
explained that the modification would allow the Department to make an
interim classification decision for a new product and then have up to
one year to hold a public hearing to determine the appropriate
permanent classification.
The DFA/DLC witness also testified in support of Proposal 2. The
witness said that its adoption would recognize the importance of dairy
proteins in the marketplace by including all dairy protein sources,
including whey and whey products, in computing the product's protein
content. However, said the witness, while whey and whey products would
be used in classification determinations, those ingredients should not
be priced as Class I.
A post-hearing brief submitted on behalf of DFA/DLC reiterated
support for adopting a protein standard. The brief reiterated the claim
that new technology has enabled some products that contain less than
6.5 percent nonfat milk solids to be classified at a lower use-value
than competitors in the market. The brief maintained that adoption of a
protein standard would more adequately identify products that should be
classified as fluid milk products in light of new fractionation
technology.
A witness appearing on behalf of O-AT-KA Milk Products Cooperative,
Inc. (O-AT-KA) testified in support of Proposals 2 and 7. O-AT-KA, at
the time of the hearing, was a cooperative owned by the dairy farmer-
members of Upstate Farms Cooperative, Inc., Niagara Milk Cooperative,
Inc., and Dairylea Cooperative, Inc. The witness was of the opinion
that the development of new technology necessitates a change to the
fluid milk product definition. However, the witness cautioned that
changes should not capture all beverages which contain milk solids as
fluid milk products because not all milk-containing beverages compete
with fluid milk.
The O-AT-KA witness asserted that Proposal 7 should not be thought
of as a fundamental change to the current standard; rather that the
proposed true protein standard of 2.25 percent is an equivalent to the
current 6.5 percent nonfat milk solids standard and should be
considered as a needed clarification brought about by technological
advances in milk processing. According to the witness, the proposed
2.25 percent standard recognizes protein as a highly valued ingredient
in milk products and those products with less than 2.25 percent protein
would remain exempt from fluid milk product classification. The witness
also advocated the adoption of Proposal 2 that would include whey and
whey products in the computation of the protein percentage of the
product but would not price the whey ingredients at Class I prices.
A post-hearing brief, submitted on behalf of O-AT-KA, reiterated
support for Proposal 7. The brief claimed that the adoption of the
protein standard would increase the use of dairy ingredients in
beverages which are not ``in the competitive sphere of the traditional
milk beverages,'' thus increasing producer revenue. The brief also
supported DFA/DLC's modification to Proposal 7 giving the Department
authority to make an interim classification decision if a new product
is a result of new technology.
Comments and exceptions to the Recommended Decision submitted on
behalf of DFA, DLC, O-AT-KA and Upstate Farms Cooperative Inc.,
hereinafter referred to as ``DFA, et al.'', supported the
recommendation incorporating a 2.25 percent true protein standard as a
proposal in the Recommended Decision and that inclusion of all milk
derived ingredients when computing the 6.5 percent nonfat solids or
2.25 percent true protein criterion. The DFA, et al., comments also
endorsed the comments and exceptions submitted on behalf of NMPF.
DFA, et al., expressed opposition to exempting casein and
caseinates from Class I pricing when used in fluid milk products. The
comments argued that all proteins in a fluid milk product should be
priced the same--at the Class I price. DFA, et al., also abandoned
their position taken at the hearing to not price whey derived from
cheese making at the Class I price when used in fluid milk products.
DFA, et al., was of the opinion that providing exemption for
ingredients will only serve to encourage manufacturers to use price-
exempted ingredients to formulate a finished product that would be
compositionally identical to fluid milk.
DFA, et al., took exception to relying on form and intended use as
the final determinate in classifying fluid milk products. DFA, et al.,
argued that manufacturers rely on the compositional criteria contained
in the fluid milk product definition to decide how to formulate a new
product, assess how their new product would be classified, and
ultimately determine their raw milk ingredient costs. Their exceptions
asserted if form and intended use criteria supersedes compositional
standards, manufacturers would develop fewer dairy based products
because of the perceived uncertainty in how that product's ingredients
could be classified and priced. DFA, et al., argued that the 2.25
percent protein standard should be the ultimate determinate of a fluid
milk product and, if such compositional standard becomes inadequate, a
hearing could be held to establish updated compositional standards.
A post-hearing brief submitted on behalf of Select Milk Producers,
Inc. (Select) and Continental Dairy Products (Continental) expressed
support for adoption of a protein standard as a component of the fluid
milk product definition. According to the brief, Select and Continental
are dairy-farmer owned cooperatives that market milk on various Federal
orders. The brief argued that adoption of a protein standard is a
needed change to reflect changed marketing conditions brought about by
new manufacturing technology without fundamentally altering current
regulations. The brief stressed that milk proteins are valuable
ingredients in drinkable products in the market and
[[Page 33538]]
that classification and pricing determinations should be reflective of
this.
Comments to the Recommended Decision filed on behalf of Select and
Continental specifically supported the proposed adoption of a 2.25
percent true protein standard to the fluid milk product definition and
pricing of MPCs used in fluid milk products at the Class I price.
Select and Continental also endorsed the comments and exceptions filed
by NMPF.
Select and Continental's exceptions asserted that as a result of
new milk-processing technology, there is no barrier to using casein as
a substitute ingredient for MPCs. In this regard, Select and
Continental took exception to exempting casein and caseinates from
Class I pricing because it would serve to provide an incentive to
manufacturers to use them as a substitute for MPCs to avoid Class I
regulation. The brief said relying on form and intended use to override
compositional standards in making classification determinations would
add needless ambiguity and subjectivity.
A witness appearing on behalf of H.P. Hood testified in opposition
to any changes to the fluid milk product definition. The witness was of
the opinion that the fluid milk product definition should not be
amended in a manner that would classify more dairy products as fluid
milk products unless data is provided which would conclude that such
products compete directly with fluid milk and such amendments would
enhance producer revenue.
The H.P. Hood witness asserted that if Proposal 7 was adopted and
resulted in the reclassification of some products as fluid milk
products, the change would only affect a small number of products and
the enhancement of producer revenue would be minimal. If ingredient
substitution for milk occurred as a result of adopting other proposals,
the witness said, producer revenue could actually decrease. The witness
was of the opinion that adoption of proposals that broaden the fluid
milk product definition would stifle product innovation and discourage
the use of dairy-derived ingredients because of the resulting increased
costs to the manufacturer. These results, the witness said, should not
be encouraged by the Federal milk order program.
A post-hearing brief submitted on behalf of H.P. Hood reiterated
opposition to Proposal 7. The brief maintained that no disorderly
marketing conditions exist to warrant a change to the fluid milk
product definition and that proponents of the protein standard failed
to meet the burden of proof required by the AMAA to make a regulatory
change. The H.P. Hood brief reviewed many factors used by the
Department in previous classification decisions to determine the proper
classification of Class I products. The list included, but was not
limited to, demand elasticities, enhancement of producer revenue, and
product competition. The brief stated that proponents failed to provide
adequate data addressing these factors or prove that disorderly
marketing conditions exist to warrant a change, and urged the
Department to terminate the proceeding.
Comments and exceptions filed by H.P. Hood took exception to the
Recommended Decision's proposed adoption of a 2.25 percent protein
standard and its reliance on form and intended use as a primary factor
in making classification determinations. H.P. Hood reiterated its
opinion that the proponents of the protein standard did not provide
adequate justification for its adoption. Furthermore, H.P. Hood was of
the opinion that it is not proper to make regulatory changes as
preventive measures to possible disorderly marketing conditions and is
a major deviation from historical milk order policy. The exceptions
stressed that it is only proper to react to marketing conditions once
they occur. In their exceptions, H.P. Hood also presented a list of
questions regarding the application of how a product's form and
intended use would be determined by the Department. H.P. Hood claimed
that relying on form and intended use would be extremely burdensome and
serve to inhibit new product development.
A witness appearing on behalf of Leprino Foods Company (Leprino)
testified in opposition to the adoption of the 2.25 percent protein
standard contained in Proposal 7. According to the witness, Leprino
operates nine plants in the United States that manufacture mozzarella
cheese and whey products. The witness was of the opinion that a protein
standard would reclassify products such as sport and protein drinks and
yogurt smoothie products (formulated with ingredients such as whey and
whey products) as fluid milk products. The witness stressed that
broadening the fluid milk product definition to account for all dairy
derived ingredients could lessen the demand for such ingredients. The
witness speculated that manufacturers may seek out other less costly
non-dairy ingredient substitutes which would result in decreased
producer revenue.
Exceptions to the Recommended Decision filed by Leprino expressed
opposition to the adoption of a 2.25 true protein standard in the fluid
milk product definition. Leprino argued that this standard should not
be adopted unless it is modified to specifically exclude beverages that
do not resemble or compete with fluid milk. Leprino was of the opinion,
that without such exclusion, to classify products based on form and
intended use could cause many non-traditional products, such as sport
and nutritional beverages, to be classified as fluid milk products. The
end result, argued Leprino, would be a lowered demand for dairy
ingredients that may offset any revenue gains to producers by including
additional products as fluid milk products.
A witness appearing on behalf of Dannon Company, Inc. (Dannon)
testified in opposition to Proposals 2 and 7. Dannon is a wholly owned
subsidiary of the Dannon Group that produces yogurt and fresh dairy
products in 40 countries, including the United States. The witness was
opposed to the adoption of a protein standard and to the inclusion of
whey when calculating the nonfat milk solids content of a product
because, the witness said, it was not the original intent of the fluid
milk product definition to include these milk-derived ingredients. The
witness believed that adoption of a protein standard would cause more
products to be classified as fluid milk products even though they do
not compete with fluid milk. The witness argued that protein is not a
major component of fluid milk products and therefore using a protein
standard would not be appropriate for making classification
determinations. The witness speculated that if a protein standard was
adopted, it could stifle product innovation or cause food processors to
use non-dairy ingredients in their food products. The witness said that
if whey proteins are included, manufacturers may look for less
expensive non-dairy ingredients to be used as a viable substitute.
A post-hearing brief submitted on behalf of Dannon reiterated their
opposition to the adoption of a protein standard claiming that adequate
justification for such a change was not given by proponents at the
hearing and that the mere ability to test for milk proteins does not
justify its adoption.
A post-hearing brief submitted on behalf of the National Yogurt
Association (NYA) expressed opposition to Proposal 7. According to the
brief, NYA is a trade association representing manufacturers of live
and active culture yogurt products and suppliers of the yogurt
industry. The brief claimed that proponent testimony was inconsistent
regarding the proposals' impact on product classification and stated
that if
[[Page 33539]]
the 2.25 percent protein standard was adopted, at least one yogurt-
containing product would be reclassified as a fluid milk product.
The NYA brief also asserted that proponents did not provide a clear
picture of how Proposal 7 would be implemented. Specifically, the brief
noted that the following were not addressed: (1) How wet and dry whey
would be handled; (2) how whey from cheese production would be
differentiated from whey from casein production; and (3) how products
that meet the proposed 2.25 percent true protein standard and contain
whey and other proteins would be classified and priced. The NYA brief
speculated that including whey in the protein calculation would lead to
more products being classified as fluid milk products and cause
manufacturers to seek out less costly non-dairy ingredients. The
potential loss to producer revenue by substitution with non-dairy
ingredients, concluded the brief, is not supported by the record.
A post-hearing brief submitted on behalf of the National Cheese
Institute (NCI) expressed opposition to Proposal 7 and claimed that its
adoption would suppress the use of dairy-derived ingredients,
particularly whey proteins. According to the brief, NCI is a trade
association representing processors, manufacturers, marketers, and
distributors of cheese and related products. NCI claimed that
proponents of Proposal 7 did not identify any specific marketplace
disorder that would be corrected by the adoption of a protein standard
or list any product that would be reclassified if the fluid milk
product definition were amended. The brief reviewed previous rulemaking
decisions where proposals were denied because proponents failed to
demonstrate that disorderly marketing conditions were present.
The NCI brief stressed that use of dairy-derived ingredients in a
product should not automatically qualify a product as a competitor of
fluid milk or that their classification in a lower-valued use
negatively affects producer revenue. The brief further maintained that
proponents did not adequately address why whey proteins should be
included in determining if the product met the proposed protein
standard for a fluid milk product and why whey should be priced at the
Class I price. The brief concluded that whey should be excluded from
the fluid milk product definition because its inclusion would lead to
products being classified as fluid milk products even when they do not
compete with fluid milk.
A post-hearing brief submitted on behalf of Sorrento Lactalis, Inc.
(Sorrento) objected to the adoption of a protein standard. According to
the brief, Sorrento is a manufacturer that operates five cheese plants
throughout the United States. The brief stated that adoption of a milk
protein standard as part of the fluid milk product definition would
reduce the demand for dairy ingredients, especially whey proteins,
which in turn would result in increased costs to manufacturers and
reduced producer revenue.
A witness testifying on behalf of H.P. Hood was of the opinion that
if the Department found that changing the fluid milk product definition
was warranted, adoption of a modified Proposal 5 would be appropriate.
The witness said that adoption of Proposal 5 would provide the
Department with standards to determine if a dairy product with less
than 6.5 percent nonfat milk solids competes with and displaces fluid
milk sales, which would justify classification of the product as a
fluid milk product. The witness also noted that if Proposal 5 was
adopted, a new product with less than 6.5 percent nonfat milk solids
and route distribution in a Federal milk marketing area of less than 3
million pounds would be exempted from classification as a fluid milk
product. This distribution criteria, the witness explained, would allow
manufacturers to test market a new product with the assurance that it
would not be classified as a fluid milk product until the distribution
threshold was exceeded.
A witness appearing on behalf of Leprino testified in support of
Proposal 5. The witness was of the opinion that fluid milk products
should only be those products that meet the FDA standard of identity
for milk and cultured buttermilk and products that compete with milk
and cultured buttermilk. The witness testified that the fluid milk
product definition is currently too broad and as a result, has lessened
the demand for dairy ingredients in new non-traditional dairy products
because of the possibility of being classified as a fluid milk product.
The witness argued that many of these new products do not compete for
sales with fluid milk and their use of dairy-derived ingredients should
not qualify them to be defined as a fluid milk product.
The Leprino witness explained that advances in technology have
allowed the creation of dairy-derived ingredients through milk
fractionation. According to the witness, dairy manufacturers are
avoiding investing in some product innovation because of the regulatory
burden and increased costs that are associated with manufacturing a
fluid milk product.
A witness testifying on behalf of DFA/DLC was opposed to the
adoption of Proposal 5. The witness said that Proposal 5 would place an
undue burden on the Department in making classification determinations
and would also extend Class II classification to more products, neither
of which the witness supported. The post-hearing brief submitted by
DFA/DLC reiterated their opposition.
A witness appearing on behalf of Bravo! Foods International
Corporation; Lifeway Foods, Inc.; PepsiCo; Starbucks Corporation; and
Unilever United States, Inc.; testified in opposition to all proposals
that would reduce or eliminate the 6.5 percent minimum nonfat milk
solids standard, adopt a protein standard, or include whey in
determining the nonfat milk solids content of a product. Hereinafter,
these companies are referred to collectively as ``Bravo!, et al.''
A post-hearing brief submitted on behalf of Bravo!, et al., urged
the termination of the proceeding except for the portion addressing the
exemption of yogurt and kefir products from the fluid milk product
definition. Bravo!, et al., asserted that the hearing record does not
support adoption of a protein standard. The brief stated that decisions
to amend Federal order provisions are not made without clear evidence
of disorderly market conditions, the potential shortage of milk for
fluid use, or lowering of producer revenue. The brief also discussed
letters sent to the Department by producers and manufacturers which
urged that a hearing be postponed because more analysis and market data
was needed to justify amending the current fluid milk product
definition. Bravo!, et al., argued that the hearing was held
prematurely, without allowing for adequate study and market data
research on the proposals that are under consideration. According to
the brief, more time was needed to accurately determine the impact of
new milk products on the marketplace.
The Bravo!, et al., brief summarized hearing testimony from
previous Department rulemaking decisions in which no changes were
recommended due to a lack of evidence to support a regulatory change.
According to Bravo!, et al., proponents did not provide evidence of
disorder in the marketplace nor did they substantiate their claims that
products currently in the market would not be reclassified if a protein
standard was adopted. On the basis of such conditions, the brief
concluded
[[Page 33540]]
that the current fluid milk product definition is adequate.
If the Department did not terminate the proceeding, the Bravo!, et
al., brief recommended that the 6.5 percent nonfat milk solids
standards remain, that the computation of nonfat milk solids not be
made on a milk equivalency basis, and that whey and whey ingredients be
excluded from the computation.
Exceptions to the Recommended Decision filed by Bravo!, et al.,
opposed the proposed adoption of the 2.25 percent protein compositional
standard and reiterated that adoption of a protein standard would have
a negative effect on dairy product innovation as manufacturers would
use lower priced non-dairy proteins as substitutes. Bravo!, et al.,
asserted that the Department did not give enough consideration to the
lowering of producer revenue that could occur due to the predicted
ingredient substitution.
Exceptions filed by Bravo!, et al., also opposed the Department's
use of form and intended use as one of the factors in making
classification determinations. The comments acknowledged that the AMAA
authorized the Federal Milk Marketing Order (FMMO) program to rely on
form and intended use in making classification determinations. However,
Bravo!, et al., asserted that historically the FMMO program applied the
form and use criteria by using compositional standards. Bravo!, et al.,
claimed that by specifically including the form and intended use
criteria in the order language the Department could ignore a product's
composition and arbitrarily classify products as fluid milk products
even though they did not compete with fluid milk. Bravo!, et al.,
predicted that the specific inclusion of form and intended use in the
fluid milk product definition would hamper the development of new
products and the use of dairy ingredients because of the uncertainty
manufacturers could face in how the milk components of their products
would be classified.
A witness appearing on behalf of Fonterra USA, Inc. (Fonterra)
testified in opposition to proposals that would include MPCs in
determining if the product met the protein standard of the fluid milk
product definition. Fonterra at the time of the hearing was a wholly
owned subsidiary of Fonterra Co-operative Group Limited, a New Zealand
based dairy cooperative owned by 12,000 New Zealand dairy farmers.
Fonterra operates plants within the United States that produce, among
other things, MPCs. The witness stressed that changes to the fluid milk
product definition would increase ingredient costs, discourage
manufacturing companies from using dairy ingredients in their products,
and force those companies to seek other less costly substitutes such as
soy and soy products.
A post-hearing brief submitted on behalf of Fonterra reiterated
their objection to changing the nonfat milk solids standard and
predicted that adoption of a protein standard would make classification
decisions unnecessarily complicated without providing additional
benefits to producers. The brief asserted that the hearing record did
not contain a sufficient economic analysis on the possible benefits
that adopting a protein standard would have on producer revenue or its
impact on the dairy industry.
The Fonterra brief speculated that adoption of a milk protein
standard would decrease the market price for milk proteins, discourage
new product development, and encourage the substitution of producer
milk with non-dairy ingredients. The brief noted that the annual growth
rate of soy and soy products in nutritional products from 1999 to 2003
was 16.5 percent, while the growth of milk proteins in nutritional
products only increased 10.1 percent over the same time period. The
brief predicted that if protein prices rise as a result of the adoption
of a milk protein standard, the growth of soy proteins will likely
increase because they could be substituted for more costly milk
proteins.
The Fonterra brief also stated that the hearing record does not
reveal disorder in the market by the application of the current fluid
milk product definition and therefore concluded that amending the fluid
milk product definition is not justified. The Fonterra brief argued
that proponents did not provide adequate reasoning for including whey
proteins in determining if a product met the protein standard but not
pricing whey proteins the same as other milk proteins. Furthermore, the
brief stated that proponents did not propose a method for
differentiating between whey proteins resulting from cheese production
and whey proteins from other sources.
Comments filed on behalf of Fonterra took exception to the
Recommended Decision's proposed adoption of a 2.25 percent true milk
protein compositional standard. Fonterra reiterated that proponents did
not meet the burden of proof needed to substantiate the adoption of a
protein standard. According to the comments, proponents did not
indicate if adoption of the standard would remedy any indications of
market disruption or reclassify some products as fluid milk products.
Fonterra's comments reviewed numerous rulemaking proceedings in
which, Fonterra concluded, the Department declined to adopt proposed
changes to marketing orders because of a lack of evidence that a change
would promote orderly marketing conditions. Fonterra argued that the
Recommended Decision did not adequately consider evidence asserting
that adoption of the milk protein standard would not increase the cost
for dairy ingredients, encourage the substitution of lower cost non-
dairy ingredients, and ultimately lower producer revenue. Fonterra was
of the opinion that before making a Final Decision, further analysis of
the proposals was needed to fully evaluate the possible economic impact
to producers and manufacturers as a result of adoption of the protein
standard.
Fonterra stated that the Department's recommended adoption of an
``either/or'' use of the protein and nonfat solids standard was not
contained in any proposal discussed at the hearing and that the
Department did not adequately explain how the use of both a protein and
nonfat solids standard would provide for the orderly marketing of milk
or increase producer revenue.
The comments filed by Fonterra also argued that the Department uses
this rulemaking proceeding to justify a change in policy that the
Department previously attempted to adopt without undertaking the formal
rulemaking process. Fonterra stated that historical Departmental policy
has been to exempt such products as casein, sodium caseinate, lactose,
whey, and MPCs from use in the nonfat milk solids calculation of a
product. In 2004, Fonterra said, the Department attempted to include
MPCs and other previously exempted dairy ingredients in the nonfat
solids calculation; however, that administrative decision was
overturned by an Administrative Law Judge. Fonterra claimed that
proposing to include all milk derived protein ingredients in the
calculation of a product's nonfat solids or protein composition is an
attempt to change historical policy without adequate analysis or
justification.
Fonterra also took exception to having some ingredients included in
the calculation of a product's composition but would not be priced in a
final product. Fonterra claimed that whey is used in nearly identical
products as MPCs and should therefore be priced the same. Fonterra was
of the opinion that pricing whey and MPCs differently would violate the
United States' World Trade Organization obligations. Fonterra
[[Page 33541]]
characterized whey production as primarily domestic, but that most MPCs
are imported. Accordingly, they concluded that excluding whey from
Class I pricing essentially places an illegal tariff on imported MPCs.
A witness appearing on behalf of the American Beverage Association
(ABA) testified in opposition to all proposals seeking to amend the
fluid milk product definition. ABA is a trade association that
represents beverage producers, distributors, franchise companies, and
their supporting industries. The witness was of the opinion that the
current fluid milk product definition already properly classifies dairy
products and that there is insufficient evidence to warrant any
changes. The witness claimed that any change would broaden the fluid
milk product definition to include products that contain only small
amounts of milk. The witness argued that many new beverage products
which contain small amounts of milk or milk ingredients do not compete
with fluid milk but do compete with soft drinks, juices and bottled
water. The witness asserted that amending the fluid milk product
definition to include some dairy ingredients not currently considered
would increase manufacturers cost of production, result in stifled
innovation of new products and encourage the use of non-dairy
ingredients as substitutes for milk-derived ingredients.
A witness appearing on behalf of Ohio Farmers Union (OFU) testified
in opposition to any change to the fluid milk product definition. OFU
is a nonpartisan, grassroots, general farm organization representing
more than 300,000 family farms nationwide according to their web site.
The witness testified that the primary purpose of the order program was
to provide consumers with a reliable supply of safe and wholesome milk.
The witness asserted that MPCs, caseinates, whey proteins, and other
similar milk-derived ingredients have functional and nutritional
characteristics different than fluid milk. Accounting for those
ingredients in the fluid milk product definition, the witness said,
would undermine the goal of the order program. The witness stressed
that if the fluid milk product definition were amended, consumer
confidence in the long established perception of milk as a fresh, pure
and wholesome beverage would be diminished and would thus threaten the
economic viability of domestic producers.
A witness appearing on behalf of the Milk Industry Foundation (MIF)
testified in opposition to amending the fluid milk product definition.
According to the witness, MIF is an organization with over 100 member
companies that process and market approximately 85 percent of the fluid
milk and fluid milk products consumed nationwide. The witness stated
that simply because a beverage contains milk or other dairy-derived
ingredients does not prove that those products compete with fluid milk
or that such competition lowers producer revenue.
The MIF witness asserted that previous Federal milk order
rulemaking decisions have required data and analysis to prove that an
amendment was warranted. According to the witness, the proponents of
proposals for changing the fluid milk product definition did not
provide such data and analysis. Along this theme, the witness said that
proponents should have provided data such as the market share held by
products that do not fall under the current fluid milk product
definition but would be included under any proposed change, cross price
elasticity of demand analysis of products which meet the existing fluid
milk product definition and of products that would be classified as a
fluid milk product if any of their proposals were adopted, and an own-
price elasticity of demand analysis for products that would be
reclassified.
A post-hearing brief submitted on behalf of MIF reiterated their
opposition to any changes to the current fluid milk product definition.
The brief urged that if the Department does amend the fluid milk
product definition, it should exclude all whey-derived protein products
in determining if a product meets the fluid milk product definition.
The brief stated that MIF has continuously opposed a hearing to
consider amending the fluid milk product definition because not enough
evidence is available to warrant a change. The brief maintained that
proponents did not offer adequate data at the hearing to demonstrate
that there is disorder in the marketplace that can be remedied by
adoption of a protein standard.
The MIF brief expanded its testimony by citing numerous rulemaking
decisions that denied proposals on the basis that adequate evidence was
not presented to warrant amendments to order provisions. MIF stressed
that the mere existence of beverages containing dairy-derived
ingredients is not evidence of marketwide disorder.
Exceptions filed on behalf of International Dairy Foods Association
(IDFA) asserted that because evidence doesn't demonstrate a need for
change, no changes to the fluid milk product definition should be made.
IDFA is a trade organization whose members include MIF, NCI and the
International Ice Cream Association (IICA). According to their
exceptions, IDFA represents more than 85 percent of the milk, cultured
products, cheese and frozen desserts produced and marketed in the
United States. IDFA reiterated arguments expressed by MIF at the
hearing and in MIF's post-hearing brief. Their exception claimed that
the hearing record did not demonstrate that products containing less
than 6.5 percent nonfat solids and more than 2.25 percent protein are
causing disorderly marketing conditions because they are not currently
classified as fluid milk products.
IDFA's comments also opposed the specific inclusion of the form and
intended use criteria in the fluid milk product definition and argued
that the definition should continue to contain only compositional
criteria. IDFA wrote that manufacturers' product development decisions
are in part determined by ingredient costs. Subjective criteria such as
form and intended use, wrote IDFA, could impede new product development
because a manufacturer would be uncertain of ingredient costs until a
final product had been classified. IDFA's exceptions opposed the
inclusion of whey when computing a product's composition because of
inconsistent justification by proponents as to why whey used to produce
fluid milk products should not also be priced as Class I. IDFA
exceptions stated that the proponents of the protein standard did not
demonstrate that disorderly marketing conditions exist in the absence
of the protein standard. IDFA exceptions concluded that the adoption of
amendments proposed in the Recommended Decision would only serve to
lower producer revenue.
Comments filed on behalf of Grande Cheese opposed all the proposed
changes to the fluid milk product definition contained in the
Recommended Decision. Grande Cheese is a cheese manufacturer located in
the State of Wisconsin. Grande Cheese expressed support of the opinions
expressed in the exceptions to the Recommended Decision filed by IDFA.
A witness appearing on behalf of the National Family Farm Coalition
testified in opposition to all proposals that would amend the fluid
milk product definition. The witness testified that MPCs do not meet
FDA's Generally Recognized as Safe (GRAS) standards as legal food
ingredients. Furthermore, the witness said, MPCs have not been
subjected to scientific testing to determine if they are safe for human
[[Page 33542]]
consumption and should not be allowed in milk products.
A witness appearing on behalf of Public Citizen testified in
opposition to proposals that seek to amend the fluid milk product
definition. According to the witness, Public Citizen is a non-profit
consumer advocacy organization with approximately 150,000 members. The
witness was opposed to any change in the fluid milk product definition
that would, in the witness' opinion, encourage the use of MPCs.
Two Pennsylvania dairy farmers testified in opposition to any
change to the fluid milk product definition. The producers opposed all
proposals that would allow the use of caseinates and MPCs in fluid milk
products. They asserted that MPCs are not allowed in the production of
standardized cheese and should also not be allowed in the production of
fluid milk products.
A post-hearing brief submitted on behalf of the American Dairy
Products Institute (ADPI), an association representing manufacturers of
dairy products, offered support for amending the fluid milk product
definition to include milk beverages that compete directly with fluid
milk. However, the brief cautioned against developing a fluid milk
product definition that would include non-traditional beverages and
smoothie type products (yogurt-containing beverages). The brief
recommended that an economic study be conducted to determine the
possible impacts of the proposed changes before action is taken to
amend the fluid milk product definition.
A post-hearing brief submitted on behalf of General Mills contended
that the fluid milk product definition should not be amended because
proponents did not provide sufficient evidence or data to justify a
change. The brief maintained that the hearing record is not clear on
how proposals would be implemented or on the impact to producers,
manufacturers, and consumers if the protein standard was adopted.
General Mills contended that before a change is made, the Department
should conduct an economic analysis to evaluate how protein and dairy
products are competing in the marketplace and how the adoption of a
protein standard would impact the marketplace. If a protein standard
was recommended for adoption, General Mills recommended that whey not
be included in the protein calculation, or if whey is included, that a
2.8 percent protein standard be adopted in order to maintain the status
quo.
Exceptions to the Recommended Decision filed by General Mills
opposed the adoption of the true protein compositional standard.
However, General Mills was of the opinion that if the Department
continued to support the protein standard, then any whey components
should be excluded from determining a final product's protein content.
General Mills purported that the inclusion of whey in the protein
calculation, even if not priced at Class I, may lead manufacturers to
increase their use of non-dairy ingredients as substitutes.
General Mills was also opposed to relying on form and intended use
in classification determinations. According to their exceptions, the
form and use criteria would cause manufacturers to be less certain of a
product's classification which would discourage using dairy ingredients
in new products. General Mills noted that if the Department decides to
not alter its Recommended Decision then it should clarify in a Final
Decision that only products that compete with or are a substitute for
fluid milk would be classified as a fluid milk product.
A post-hearing brief submitted on behalf of New York State Dairy
Foods, Inc. (NYSDF) opposed amending the fluid milk product definition.
According to their brief, NYSDF is a trade association representing
dairy product processors, manufacturers, distributors, retailers, and
producers in the Northeast United States. The brief argued that
products produced with the use of new fractionation technology are a
small portion of the milk beverage market. They were of the opinion
that such products are still too new to determine their impact on Class
I sales and producer revenue. The brief also asserted that the adoption
of a protein standard as part of the fluid milk product definition
would discourage new product development and would increase costs that
would result in reduced sales of dairy-derived ingredients. The brief
urged that the proceeding be terminated.
Comments and exceptions to the Recommended Decision filed on behalf
of Glanbia Foods (Glanbia) opposed the proposed adoption of the true
protein compositional standard and the specific inclusion of form and
intended use as a factor in classification determinations. Glanbia
operates two cheese plants and two whey plants that collectively
process nearly 4 billion pounds of milk annually. Glanbia asserted that
adoption of a true protein standard would lead to stifled innovation of
milk derived ingredients in new products because the manufacturing