Agency Information Collection Activities; Proposed Collection; Comment Request; Restaurant Menu and Vending Machine Labeling: Recordkeeping and Mandatory Third Party Disclosure Under Section 4205 of the Patient Protection and Affordable Care Act of 2010, 68361-68364 [2010-28014]
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68361
Federal Register / Vol. 75, No. 214 / Friday, November 5, 2010 / Notices
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
List of Ingredients Added to Tobacco
in the Manufacture of Cigarette
Products—Extension—Office on
Smoking and Health, National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
Cigarette smoking is the leading
preventable cause of premature death
and disability in the United States. Each
year, more than 440,000 premature
deaths occur as the result of diseases
related to cigarette smoking. The
Centers for Disease Control and
Prevention (CDC), Office on Smoking
and Health (OSH) has the primary
responsibility for the Department of
Health and Human Services (HHS)
smoking and health program. HHS’s
overall goal is to reduce death and
disability resulting from cigarette
smoking and other forms of tobacco use
through programs of information,
education and research.
The Comprehensive Smoking
Education Act of 1984 (CSEA, 15 U.S.C.
1336 or Public Law 98–474) requires
each person who manufactures,
packages, or imports cigarettes to
provide the Secretary of Health and
Human Services (HHS) with a list of
ingredients added to tobacco in the
manufacture of cigarettes. The
legislation also authorizes HHS to
undertake research, and to report to the
Congress (as deemed appropriate)
discussing the health effects of these
ingredients.
HHS has delegated responsibility for
implementing the CSEA’s ingredient
reporting requirements to CDC’s Office
on Smoking and Health (OSH). OSH has
collected ingredient reports on cigarette
products since 1986. Respondents are
commercial cigarette manufacturers,
packagers, or importers, or their
designated representatives. Respondents
are not required to submit specific
forms, however, they are required to
submit a list of all ingredients used in
their products. CDC requires the
ingredient report to be submitted by
chemical name and Chemical Abstract
Service (CAS) Registration Number,
consistent with accepted reporting
practices for other companies currently
required to report ingredients added to
other consumer products. Typically,
respondents submit a summary report to
CDC with the ingredient information for
multiple products, or a statement that
there are no changes to their previously
submitted ingredient report.
Ingredient reports for new products
are due at the time of first importation.
Thereafter, ingredient reports are due
annually on March 31. Information is
submitted to OSH by mailing a written
report on the respondent’s letterhead, by
CD, three-inch floppy disk, or thumb
drive. Electronic mail submissions are
not accepted. Upon receipt and
verification of the annual ingredient
report, OSH issues a Certificate of
Compliance to the respondent.
There are no costs to respondents
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
No. of
respondents
Type of respondents
Cigarette Manufacturers, Packagers, and Importers .......................................
Dated: November 1, 2010.
Carol E. Walker,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–27983 Filed 11–4–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
mstockstill on DSKH9S0YB1PROD with NOTICES
[Docket No. FDA–2010–N–0567]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Restaurant Menu
and Vending Machine Labeling:
Recordkeeping and Mandatory Third
Party Disclosure Under Section 4205 of
the Patient Protection and Affordable
Care Act of 2010
AGENCY:
Food and Drug Administration,
HHS.
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ACTION:
143
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal Agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the recordkeeping and mandatory third
party disclosure provisions of Section
4205 of the Patient Protection and
Affordable Care Act of 2010 (ACA).
DATES: Submit either electronic or
written comments on the collection of
information by January 4, 2011.
ADDRESSES: Submit electronic
comments on the collection of
SUMMARY:
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Fmt 4703
Sfmt 4703
Average burden per response
(in hours)
No. of responses per
respondent
1
6.5
Total burden
hours
930
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3793.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
Agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined in
44 U.S.C. 3502(3) and 5 CFR 1320.3(c)
and includes agency requests or
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mstockstill on DSKH9S0YB1PROD with NOTICES
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires Federal Agencies
to provide a 60-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Restaurant Menu and Vending Machine
Labeling: Recordkeeping and Mandatory
Third Party Disclosure Under Section
4205 of the Patient Protection and
Affordable Care Act of 2010—(OMB
Control Number 0910–0665)—Revision
On March 23, 2010, the President
signed into law the ACA (Pub. L. 111–
148). Section 4205 of the legislation,
which principally amends sections 403
and 403A of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C. 343 and
343–1), requires chain restaurants and
similar retail food establishments
(SRFE) with 20 or more locations doing
business under the same name and
offering for sale substantially the same
menu items (hereinafter ‘‘chain retail
food establishments’’), as well as
operators of 20 or more vending
machines (hereinafter ‘‘chain vending
machine operators’’), to disclose certain
nutrition information for certain food
items offered for sale so that consumers
can make more informed choices about
the food they purchase. Section 4205
preempts State and local governments
from establishing menu labeling
requirements for chain retail food
establishments and vending machine
nutrition labeling requirements that are
not ‘‘identical to’’ the section 4205
requirements.
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Section 4205 became effective on the
date the law was signed, March 23,
2010. The provisions that went into
immediate effect are as follows:
For chain retail food establishments:
• Disclosing the number of calories in
each standard menu item on menus and
menu boards,
• Making additional written nutrition
information available to consumers
upon request,
• Providing a statement on menus
and menu boards about the availability
of the written nutrition information, and
• Providing calorie information (per
serving or per food item) for self-service
items and food on display, in a sign
adjacent to each food item.
For chain vending machine operators:
• Providing a sign in close proximity
to each article of food (or the selection
button) that discloses the number of
calories contained in the article, unless
a prospective purchaser is able to
examine the Nutrition Facts Panel
before purchasing the article, or visible
nutrition information is otherwise
provided at the point of purchase.
Section 4205 of the legislation
requires recordkeeping—for the calorie
analysis—and a third party disclosure—
for the menu and vending machine
labeling.
In the Federal Register of August 25,
2010 (75 FR 52427), FDA published a
notice of availability of the guidance
document entitled ‘‘Guidance for
Industry: Questions and Answers
Regarding the Effect of Section 4205 of
the Patient Protection and Affordable
Care Act of 2010 on State and Local
Menu and Vending Machine Labeling
Laws.’’ The guidance is intended to
clarify section 4205’s effect on State and
local menu and vending machine
labeling laws, and to ensure that
industry and State and local government
understand the immediate effects of the
law. Persons with access to the Internet
may obtain the guidance at the
following Web site: https://
www.cfsan.fda.gov/∼dms/
guidance.html. In addition, the
information collection requirements
were approved under the emergency
processing provisions of the PRA and
assigned OMB control number 0910–
0665.
Menu and vending machine labeling
will be used by consumers to assess the
calorie content of their purchases. The
purpose of the disclosure is to allow
consumers to choose foods that are
appropriate for their energy needs.
Because consumers do not observe the
preparation of food prepared by
restaurants or similar retail food
establishments, and because many of
these foods were exempted from
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Fmt 4703
Sfmt 4703
nutrition labeling requirements under
the National Labeling Education Act
(NLEA), consumers were not able to
ascertain the calorie content of this
food, and therefore could not make
informed decisions about how that food
fits their calorie requirements without
the disclosure. The calorie information
will be collected and recorded by the
chain retail food establishments and
chain vending machine operators that
are required to disclose calorie
information to their customers. The
covered entities will use the records to
ensure that calorie information that they
disclose is accurate.
Description of Respondents:
Respondents to this collection of
information include chain retail food
establishments and chain vending
machine operators.
FDA estimates the burden of this
collection of information as follows. The
burden is described in the following
paragraphs in two parts: A
recordkeeping burden associated with
discovering and recording the calorie
count for each menu/vending item; and
the third party disclosure burden
associated with communicating that
information to the consumer. The
estimates are also separated for retail
food service and vending operators.
FDA estimates a total of 1,388,010
initial burden hours. This number has
been divided by three in tables 1 and 2
of this document in order to avoid
double counting in the Regulatory
Information Service Center (RISC) and
Office of Information and Regulatory
Affairs (OIRA) Consolidated Information
System to yield 141,222 initial hours for
recordkeeping and 312,448 initial hours
for third party disclosure, for a sum of
462,670 initial hours. FDA estimates a
total of 14,068,808 recurring hours, with
nearly all of these for vending machine
operators, including 31,408 recurring
hours for recordkeeping and 14,037,400
recurring hours for third party
disclosure.
Recordkeeping Burdens for Chain
Retail Food Establishments
The time burden for calorie analysis
on chain retail food establishments is
the time necessary for creating a record,
managing the contracts for analysis, and
communicating the results of the
analysis to the outlets. FDA estimates
the hourly burden of calorie analysis on
these firms to be 4 hours per menu item.
FDA estimates that there are
approximately 1,069 restaurant chains,
with 231,000 outlets, will be required to
disclose calorie information. On
average, we estimate that a chain has
117 items on its menu, and that 48
percent of chain restaurants, or 516, do
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Federal Register / Vol. 75, No. 214 / Friday, November 5, 2010 / Notices
not already have calorie information.
The hourly burden for restaurant chains
is 241,488 hours (= 516 chains × 117
items/chain × 4 hours/item).
FDA estimates that there are 570
covered grocery and convenience store
chains with an average of 40 standard
menu items per chain. The hourly
burden for grocery store chains is 91,200
hours (= 570 chains × 40 items/chain ×
4 hours/item).
FDA estimates that there are 420 other
chains that will be covered by the
proposed rule. With 40 menu items on
average, the number of hours required to
deal with calorie analysis at these other
chains is 67,200 hours (= 420 chains ×
40 items/chain × 4 hours/item).
FDA has estimated that each of the
1,506 covered chains, on average,
introduces new items or reformulates
existing items 4 times per year. The
recurring hourly burden of
recordkeeping for new items, as
displayed in the sixth row of table 1 of
this document, is 24,096 hours (= 1,506
chains × 4 items/chain × 4 hours/item).
FDA estimates that 30 chains will
become newly covered under the
requirements of the proposed rule each
year. With an average number of menu
items of 60 per chain, this would result
in approximately 7,200 hours (= 30
chains × 60 items/chain × 4 hours/item).
This amount is displayed in the seventh
row of table 1 of this document.
The final column of table 1of this
document gives the estimated capital
costs associated with calorie and
nutrition analysis. These are the costs of
acquiring nutrition analyses. FDA has
estimated that the average cost of a full
analysis is $269 per menu item. These
costs are calculated by multiplying this
per item cost by the number of items in
column three multiplied by the number
of recordkeepers in column two.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL RECORDKEEPING BURDEN: CALORIE ANALYSIS AND RECORDING 1
Number of
recordkeepers
Type of respondent
Annual frequency per
recordkeeper
Total annual
records
Hours per
record
Total hours
Total capital
costs
Restaurant Chains ...................................
Grocery and Convenience Store Chains
Other Chains ...........................................
Vending Operators ..................................
516
570
420
600
117
40
40
20
60,372
22,800
16,800
12,000
4
4
4
2
241,488
91,200
67,200
24,000
$16.2 million
$6.1 million
$4.5 million
$0,000
Total Initial Hours .............................
New/Reformulated Items .........................
New Chains .............................................
New Vendors ...........................................
1,506
30
3
4
60
20
6,024
1,800
60
4
4
2
423,888
24,096
7,200
120
$26.9 million
$1.6 million
$0.5 million
$4,000
Total Recurring Hours ......................
1
31,416
There are no operating and maintenance costs associated with this collection of information.
mstockstill on DSKH9S0YB1PROD with NOTICES
Third Party Disclosure Burdens for
Chain Retail Food Establishments
The third party reporting burden for
chain retail food establishments is the
time necessary to display calorie
information on menus, menu boards,
displayed food and other required
locations. In practice, this is the time
necessary to change out redesigned
menu boards, FDA estimates 2 hours of
time per menu board change.
FDA estimates that limited service
restaurant chains have an average of
three menu boards or displays per
establishment. With 135,705 outlets
having these displays, the total hourly
burden estimated for third party
disclosure at restaurants is 814,230
hours (= 135,705 outlets × 3 displays/
outlet × 2 hours/display).
For grocery and convenience store
chains, FDA estimates an average of
1 major menu board or display per
establishment. With 41,945 outlets, the
total hourly burden is 83,890 hours (=
41,945 outlets × 1 displays/outlet × 2
hours/display).
For other covered chains, FDA
estimates 33,114 covered outlets, each
with an average of one major display or
menu board. At 4 hours per disclosure,
FDA estimates an hourly burden of
66,228 hours (= 33,114 outlets × 1
displays/outlet × 2 hours/display).
The most inexpensive technology
available to vending machine operators
for disclosing calorie content is using
stickers. Because these do not require
any initial investment and because they
are not durable, all burden and costs
will be on a recurring basis.
Recurring Disclosure Burdens for Chain
Retail Food Establishments
FDA estimates that the annual
number of newly covered chains will be
30. At 20 establishments per chain,
there will be 600 establishments at
newly covered chains each year that
will need to disclose calorie content.
Taking an average number of displays
equal to 2, the total hourly burden for
disclosure due to newly covered chains
is 2,400 hours (= 600 outlets × 2
displays/outlet × 2 hours/display).
The final column of table 2 of this
document gives the estimated capital
costs associated with third party
disclosure. These are the costs of
acquiring new menu boards or displays.
FDA has estimated that the average cost
of menu board to be $550. These costs
are calculated by multiplying this per
menu board cost by the frequency of
disclosures in column three multiplied
by the number of respondents in
column two.
TABLE 2—ESTIMATED ANNUAL THIRD PARTY DISCLOSURE BURDEN: CALORIE CONTENT 1
Number of
respondents
Type of respondent
Restaurants ..............................................................
Grocery and Convenience Store Chains .................
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Annual
frequency per
disclosure
135,705
41,945
Frm 00049
Fmt 4703
Total annual
disclosures
3
1
Sfmt 4703
Hours per
disclosure
407,115
41,945
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2
2
Total hours
814,230
83,890
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Federal Register / Vol. 75, No. 214 / Friday, November 5, 2010 / Notices
TABLE 2—ESTIMATED ANNUAL THIRD PARTY DISCLOSURE BURDEN: CALORIE CONTENT 1—Continued
Number of
respondents
Type of respondent
Other Chains ............................................................
Annual
frequency per
disclosure
33,114
Total annual
disclosures
1
Hours per
disclosure
33,114
Total hours
2
66,228
Total Initial Hours .......................................................................................................................................................................
New SRFE Outlets ...................................................
600
2
1,200
2
Vending (Ongoing) ...................................................
5,000
56,000
280,000,000
0.05
Vending (Growth) .....................................................
5,000
140
700,000
0.05
964,348
2,400
14,000,000
35,000
Total Recurring Hours ................................................................................................................................................................
14,037,400
1There
are no operating and maintenance costs associated with this collection of information.
mstockstill on DSKH9S0YB1PROD with NOTICES
Burdens for Chain Vending Machine
Operators
Because almost all vending machines
sell food that is previously
manufactured and packaged, calorie
analysis and production of calorie
analysis displays will be most
efficiently done at the manufacturer
level instead of the operator level.
Furthermore, most vended foods are
subject to NLEA, which means that
calorie content is already collected. A
likely scenario for response to vending
machine labeling is that food
manufacturers include a set of calorie
label stickers in each case of product.
This would be efficient both because
most manufacturers will already have
the calorie information available, and
because economies of scale exist for the
manufacturer. In this case, vending
machine operators will not need to keep
a record of calorie content. Instead, the
burden for most operators will be
limited to that of administering records
and passing the existing information on
to consumers.
FDA estimates that there are
approximately 300,000 beverage
machines that sell unpackaged
products. The manufacturer of the
ingredients to these foods (hot coffee
drinks and sodas) would not necessarily
have calorie information if the products
were not subject to NLEA in some form.
There are likely a limited number of
manufacturers of the inputs to the
beverage machines. For the purposes of
this document, FDA estimates that there
are 10 manufacturers serving these
machines, and 20 drinks per
manufacturer, so that approximately 200
drinks would need to have calorie
analysis. The cost of this calorie
analysis will be included in the capital
costs in the following paragraphs. FDA
estimates that the recordkeeping burden
for these firms is half that for
restaurants, or two hours per item. If
there are 600 firms using beverage
dispensers, then the hourly burden for
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recordkeeping is 24,000 hours (= 600
firms × 20 items/firm × 2 hours/item).
FDA believes that the set of items sold
in these dispensary machines is
approximately constant. If there is .5
percent growth in the number of firms,
then approximately three new firms will
become covered in this market in a
given year. The burden associated with
these three firms would be 120 hours (=
3 firms × 20 items/firm × 2 hours/item).
This amount is given in eighth row of
table 1 of this document.
The third party reporting for chain
vending machine operators is the time
necessary to install calorie displays on
their vending machines. Because there
is wide variation in the kinds of vending
machines used—in materials, display,
mechanism—there will likely be a
variety of solutions. On the high end, a
calorie display that is integrated with
the graphics on the machine may cost
several hundred dollars or more. On the
low end, a set of calorie stickers affixed
to the front of the machine would cost
at most a few dollars per machine.
Given the low margins in the vending
machine industry, and given that nearly
all of the regulated operators will be
small businesses, FDA believes that
almost all operators will, at least
initially, choose the sticker option. In
the long run, the manufacturers of
vending machines, and the larger
vending machine operators, such as the
soft drink companies, may use the more
integrated, and thus expensive, solution.
FDA tentatively estimates a recurring
hourly burden of 1 hour per machine, 2
times per year to install the displays. If
there are an average of 20 items per
machine, then the burden per response
is .05 hours (= 1 hours/machine/20
items/machine).This will be the time
necessary to decide where to put the
displays on the machine, and to sort,
remove and affix calorie stickers. FDA
expects the stickers to have a relatively
short life, and the mix of product in a
machine to change over time.
FDA estimates approximately 7
million machines are serviced by 5,000
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Sfmt 4703
operators, for an average number of
machines per operator of 1,400
machines. If each machine has 20 items,
then the average number of responses
per operator is 28,000. Given that
stickers will likely need to be replaced
twice per year on average, this number
of responses doubles, to 56,000
responses per operator. The total
recurring hours needed for third party
display is then 14 million hours (= 5000
firms × 1,400 machines/firm x 20
displays/machine × .05 hours/display ×
2). This amount is recurring in every
year, and is given in row 7 of table 2 of
this document.
If growth in the vending machine
industry is .5 percent, then each of the
5,000 respondents will have an average
of 7 additional machines that would
need to report calorie content each year.
With an average number of items per
machine of 20, the number of
disclosures per respondent is 140. At
.05 hours per response, the hours
needed to disclose calorie content on
new machines is 35,000 hours per year
(= 5000 firms × 7 machines/firm × 20
items/machine × .05 hours/item). This
amount is displayed in row 8 of table 2
of this document.
Dated: November 1, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–28014 Filed 11–4–10; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–D–0275]
Guidance for Industry and Food and
Drug Administration Staff; Class II
Special Controls Guidance Document:
Full-Field Digital Mammography
System; Availability
AGENCY:
Food and Drug Administration,
HHS.
E:\FR\FM\05NON1.SGM
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Agencies
[Federal Register Volume 75, Number 214 (Friday, November 5, 2010)]
[Notices]
[Pages 68361-68364]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-28014]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0567]
Agency Information Collection Activities; Proposed Collection;
Comment Request; Restaurant Menu and Vending Machine Labeling:
Recordkeeping and Mandatory Third Party Disclosure Under Section 4205
of the Patient Protection and Affordable Care Act of 2010
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing an
opportunity for public comment on the proposed collection of certain
information by the Agency. Under the Paperwork Reduction Act of 1995
(the PRA), Federal Agencies are required to publish notice in the
Federal Register concerning each proposed collection of information,
including each proposed extension of an existing collection of
information, and to allow 60 days for public comment in response to the
notice. This notice solicits comments on the recordkeeping and
mandatory third party disclosure provisions of Section 4205 of the
Patient Protection and Affordable Care Act of 2010 (ACA).
DATES: Submit either electronic or written comments on the collection
of information by January 4, 2011.
ADDRESSES: Submit electronic comments on the collection of information
to https://www.regulations.gov. Submit written comments on the
collection of information to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852. All comments should be identified with the docket
number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: Denver Presley, Jr., Office of
Information Management, Food and Drug Administration, 1350 Piccard Dr.,
PI50-400B, Rockville, MD 20850, 301-796-3793.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
Agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or
[[Page 68362]]
requirements that members of the public submit reports, keep records,
or provide information to a third party. Section 3506(c)(2)(A) of the
PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal Agencies to provide a
60-day notice in the Federal Register concerning each proposed
collection of information, including each proposed extension of an
existing collection of information, before submitting the collection to
OMB for approval. To comply with this requirement, FDA is publishing
notice of the proposed collection of information set forth in this
document.
With respect to the following collection of information, FDA
invites comments on these topics: (1) Whether the proposed collection
of information is necessary for the proper performance of FDA's
functions, including whether the information will have practical
utility; (2) the accuracy of FDA's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques, when
appropriate, and other forms of information technology.
Restaurant Menu and Vending Machine Labeling: Recordkeeping and
Mandatory Third Party Disclosure Under Section 4205 of the Patient
Protection and Affordable Care Act of 2010--(OMB Control Number 0910-
0665)--Revision
On March 23, 2010, the President signed into law the ACA (Pub. L.
111-148). Section 4205 of the legislation, which principally amends
sections 403 and 403A of the Federal Food, Drug, and Cosmetic Act (21
U.S.C. 343 and 343-1), requires chain restaurants and similar retail
food establishments (SRFE) with 20 or more locations doing business
under the same name and offering for sale substantially the same menu
items (hereinafter ``chain retail food establishments''), as well as
operators of 20 or more vending machines (hereinafter ``chain vending
machine operators''), to disclose certain nutrition information for
certain food items offered for sale so that consumers can make more
informed choices about the food they purchase. Section 4205 preempts
State and local governments from establishing menu labeling
requirements for chain retail food establishments and vending machine
nutrition labeling requirements that are not ``identical to'' the
section 4205 requirements.
Section 4205 became effective on the date the law was signed, March
23, 2010. The provisions that went into immediate effect are as
follows:
For chain retail food establishments:
Disclosing the number of calories in each standard menu
item on menus and menu boards,
Making additional written nutrition information available
to consumers upon request,
Providing a statement on menus and menu boards about the
availability of the written nutrition information, and
Providing calorie information (per serving or per food
item) for self-service items and food on display, in a sign adjacent to
each food item.
For chain vending machine operators:
Providing a sign in close proximity to each article of
food (or the selection button) that discloses the number of calories
contained in the article, unless a prospective purchaser is able to
examine the Nutrition Facts Panel before purchasing the article, or
visible nutrition information is otherwise provided at the point of
purchase.
Section 4205 of the legislation requires recordkeeping--for the
calorie analysis--and a third party disclosure--for the menu and
vending machine labeling.
In the Federal Register of August 25, 2010 (75 FR 52427), FDA
published a notice of availability of the guidance document entitled
``Guidance for Industry: Questions and Answers Regarding the Effect of
Section 4205 of the Patient Protection and Affordable Care Act of 2010
on State and Local Menu and Vending Machine Labeling Laws.'' The
guidance is intended to clarify section 4205's effect on State and
local menu and vending machine labeling laws, and to ensure that
industry and State and local government understand the immediate
effects of the law. Persons with access to the Internet may obtain the
guidance at the following Web site: https://www.cfsan.fda.gov/~dms/
guidance.html. In addition, the information collection requirements
were approved under the emergency processing provisions of the PRA and
assigned OMB control number 0910-0665.
Menu and vending machine labeling will be used by consumers to
assess the calorie content of their purchases. The purpose of the
disclosure is to allow consumers to choose foods that are appropriate
for their energy needs. Because consumers do not observe the
preparation of food prepared by restaurants or similar retail food
establishments, and because many of these foods were exempted from
nutrition labeling requirements under the National Labeling Education
Act (NLEA), consumers were not able to ascertain the calorie content of
this food, and therefore could not make informed decisions about how
that food fits their calorie requirements without the disclosure. The
calorie information will be collected and recorded by the chain retail
food establishments and chain vending machine operators that are
required to disclose calorie information to their customers. The
covered entities will use the records to ensure that calorie
information that they disclose is accurate.
Description of Respondents: Respondents to this collection of
information include chain retail food establishments and chain vending
machine operators.
FDA estimates the burden of this collection of information as
follows. The burden is described in the following paragraphs in two
parts: A recordkeeping burden associated with discovering and recording
the calorie count for each menu/vending item; and the third party
disclosure burden associated with communicating that information to the
consumer. The estimates are also separated for retail food service and
vending operators. FDA estimates a total of 1,388,010 initial burden
hours. This number has been divided by three in tables 1 and 2 of this
document in order to avoid double counting in the Regulatory
Information Service Center (RISC) and Office of Information and
Regulatory Affairs (OIRA) Consolidated Information System to yield
141,222 initial hours for recordkeeping and 312,448 initial hours for
third party disclosure, for a sum of 462,670 initial hours. FDA
estimates a total of 14,068,808 recurring hours, with nearly all of
these for vending machine operators, including 31,408 recurring hours
for recordkeeping and 14,037,400 recurring hours for third party
disclosure.
Recordkeeping Burdens for Chain Retail Food Establishments
The time burden for calorie analysis on chain retail food
establishments is the time necessary for creating a record, managing
the contracts for analysis, and communicating the results of the
analysis to the outlets. FDA estimates the hourly burden of calorie
analysis on these firms to be 4 hours per menu item.
FDA estimates that there are approximately 1,069 restaurant chains,
with 231,000 outlets, will be required to disclose calorie information.
On average, we estimate that a chain has 117 items on its menu, and
that 48 percent of chain restaurants, or 516, do
[[Page 68363]]
not already have calorie information. The hourly burden for restaurant
chains is 241,488 hours (= 516 chains x 117 items/chain x 4 hours/
item).
FDA estimates that there are 570 covered grocery and convenience
store chains with an average of 40 standard menu items per chain. The
hourly burden for grocery store chains is 91,200 hours (= 570 chains x
40 items/chain x 4 hours/item).
FDA estimates that there are 420 other chains that will be covered
by the proposed rule. With 40 menu items on average, the number of
hours required to deal with calorie analysis at these other chains is
67,200 hours (= 420 chains x 40 items/chain x 4 hours/item).
FDA has estimated that each of the 1,506 covered chains, on
average, introduces new items or reformulates existing items 4 times
per year. The recurring hourly burden of recordkeeping for new items,
as displayed in the sixth row of table 1 of this document, is 24,096
hours (= 1,506 chains x 4 items/chain x 4 hours/item).
FDA estimates that 30 chains will become newly covered under the
requirements of the proposed rule each year. With an average number of
menu items of 60 per chain, this would result in approximately 7,200
hours (= 30 chains x 60 items/chain x 4 hours/item). This amount is
displayed in the seventh row of table 1 of this document.
The final column of table 1of this document gives the estimated
capital costs associated with calorie and nutrition analysis. These are
the costs of acquiring nutrition analyses. FDA has estimated that the
average cost of a full analysis is $269 per menu item. These costs are
calculated by multiplying this per item cost by the number of items in
column three multiplied by the number of recordkeepers in column two.
FDA estimates the burden of this collection of information as
follows:
Table 1--Estimated Annual Recordkeeping Burden: Calorie Analysis and Recording \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Annual
Type of respondent Number of frequency per Total annual Hours per Total hours Total capital costs
recordkeepers recordkeeper records record
--------------------------------------------------------------------------------------------------------------------------------------------------------
Restaurant Chains....................... 516 117 60,372 4 241,488 $16.2 million
Grocery and Convenience Store Chains.... 570 40 22,800 4 91,200 $6.1 million
Other Chains............................ 420 40 16,800 4 67,200 $4.5 million
Vending Operators....................... 600 20 12,000 2 24,000 $0,000
---------------------------------------------------------------------------------------------------------------
Total Initial Hours................. .............. .............. .............. .............. 423,888 $26.9 million
New/Reformulated Items.................. 1,506 4 6,024 4 24,096 $1.6 million
New Chains.............................. 30 60 1,800 4 7,200 $0.5 million
New Vendors............................. 3 20 60 2 120 $4,000
---------------------------------------------------------------------------------------------------------------
Total Recurring Hours............... .............. .............. .............. .............. 31,416 ..............................
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no operating and maintenance costs associated with this collection of information.
Third Party Disclosure Burdens for Chain Retail Food Establishments
The third party reporting burden for chain retail food
establishments is the time necessary to display calorie information on
menus, menu boards, displayed food and other required locations. In
practice, this is the time necessary to change out redesigned menu
boards, FDA estimates 2 hours of time per menu board change.
FDA estimates that limited service restaurant chains have an
average of three menu boards or displays per establishment. With
135,705 outlets having these displays, the total hourly burden
estimated for third party disclosure at restaurants is 814,230 hours (=
135,705 outlets x 3 displays/outlet x 2 hours/display).
For grocery and convenience store chains, FDA estimates an average
of 1 major menu board or display per establishment. With 41,945
outlets, the total hourly burden is 83,890 hours (= 41,945 outlets x 1
displays/outlet x 2 hours/display).
For other covered chains, FDA estimates 33,114 covered outlets,
each with an average of one major display or menu board. At 4 hours per
disclosure, FDA estimates an hourly burden of 66,228 hours (= 33,114
outlets x 1 displays/outlet x 2 hours/display).
The most inexpensive technology available to vending machine
operators for disclosing calorie content is using stickers. Because
these do not require any initial investment and because they are not
durable, all burden and costs will be on a recurring basis.
Recurring Disclosure Burdens for Chain Retail Food Establishments
FDA estimates that the annual number of newly covered chains will
be 30. At 20 establishments per chain, there will be 600 establishments
at newly covered chains each year that will need to disclose calorie
content. Taking an average number of displays equal to 2, the total
hourly burden for disclosure due to newly covered chains is 2,400 hours
(= 600 outlets x 2 displays/outlet x 2 hours/display).
The final column of table 2 of this document gives the estimated
capital costs associated with third party disclosure. These are the
costs of acquiring new menu boards or displays. FDA has estimated that
the average cost of menu board to be $550. These costs are calculated
by multiplying this per menu board cost by the frequency of disclosures
in column three multiplied by the number of respondents in column two.
Table 2--Estimated Annual Third Party Disclosure Burden: Calorie Content \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Annual
Type of respondent Number of frequency per Total annual Hours per Total hours
respondents disclosure disclosures disclosure
--------------------------------------------------------------------------------------------------------------------------------------------------------
Restaurants....................................................... 135,705 3 407,115 2 814,230
Grocery and Convenience Store Chains.............................. 41,945 1 41,945 2 83,890
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 68364]]
Other Chains...................................................... 33,114 1 33,114 2 66,228
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total Initial Hours................................................................................................................ 964,348
New SRFE Outlets.................................................. 600 2 1,200 2 2,400
Vending (Ongoing)................................................. 5,000 56,000 280,000,000 0.05 14,000,000
Vending (Growth).................................................. 5,000 140 700,000 0.05 35,000
-------------------------------------------------------------------------------------
Total Recurring Hours.............................................................................................................. 14,037,400
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\There are no operating and maintenance costs associated with this collection of information.
Burdens for Chain Vending Machine Operators
Because almost all vending machines sell food that is previously
manufactured and packaged, calorie analysis and production of calorie
analysis displays will be most efficiently done at the manufacturer
level instead of the operator level. Furthermore, most vended foods are
subject to NLEA, which means that calorie content is already collected.
A likely scenario for response to vending machine labeling is that food
manufacturers include a set of calorie label stickers in each case of
product. This would be efficient both because most manufacturers will
already have the calorie information available, and because economies
of scale exist for the manufacturer. In this case, vending machine
operators will not need to keep a record of calorie content. Instead,
the burden for most operators will be limited to that of administering
records and passing the existing information on to consumers.
FDA estimates that there are approximately 300,000 beverage
machines that sell unpackaged products. The manufacturer of the
ingredients to these foods (hot coffee drinks and sodas) would not
necessarily have calorie information if the products were not subject
to NLEA in some form. There are likely a limited number of
manufacturers of the inputs to the beverage machines. For the purposes
of this document, FDA estimates that there are 10 manufacturers serving
these machines, and 20 drinks per manufacturer, so that approximately
200 drinks would need to have calorie analysis. The cost of this
calorie analysis will be included in the capital costs in the following
paragraphs. FDA estimates that the recordkeeping burden for these firms
is half that for restaurants, or two hours per item. If there are 600
firms using beverage dispensers, then the hourly burden for
recordkeeping is 24,000 hours (= 600 firms x 20 items/firm x 2 hours/
item).
FDA believes that the set of items sold in these dispensary
machines is approximately constant. If there is .5 percent growth in
the number of firms, then approximately three new firms will become
covered in this market in a given year. The burden associated with
these three firms would be 120 hours (= 3 firms x 20 items/firm x 2
hours/item). This amount is given in eighth row of table 1 of this
document.
The third party reporting for chain vending machine operators is
the time necessary to install calorie displays on their vending
machines. Because there is wide variation in the kinds of vending
machines used--in materials, display, mechanism--there will likely be a
variety of solutions. On the high end, a calorie display that is
integrated with the graphics on the machine may cost several hundred
dollars or more. On the low end, a set of calorie stickers affixed to
the front of the machine would cost at most a few dollars per machine.
Given the low margins in the vending machine industry, and given that
nearly all of the regulated operators will be small businesses, FDA
believes that almost all operators will, at least initially, choose the
sticker option. In the long run, the manufacturers of vending machines,
and the larger vending machine operators, such as the soft drink
companies, may use the more integrated, and thus expensive, solution.
FDA tentatively estimates a recurring hourly burden of 1 hour per
machine, 2 times per year to install the displays. If there are an
average of 20 items per machine, then the burden per response is .05
hours (= 1 hours/machine/20 items/machine).This will be the time
necessary to decide where to put the displays on the machine, and to
sort, remove and affix calorie stickers. FDA expects the stickers to
have a relatively short life, and the mix of product in a machine to
change over time.
FDA estimates approximately 7 million machines are serviced by
5,000 operators, for an average number of machines per operator of
1,400 machines. If each machine has 20 items, then the average number
of responses per operator is 28,000. Given that stickers will likely
need to be replaced twice per year on average, this number of responses
doubles, to 56,000 responses per operator. The total recurring hours
needed for third party display is then 14 million hours (= 5000 firms x
1,400 machines/firm x 20 displays/machine x .05 hours/display x 2).
This amount is recurring in every year, and is given in row 7 of table
2 of this document.
If growth in the vending machine industry is .5 percent, then each
of the 5,000 respondents will have an average of 7 additional machines
that would need to report calorie content each year. With an average
number of items per machine of 20, the number of disclosures per
respondent is 140. At .05 hours per response, the hours needed to
disclose calorie content on new machines is 35,000 hours per year (=
5000 firms x 7 machines/firm x 20 items/machine x .05 hours/item). This
amount is displayed in row 8 of table 2 of this document.
Dated: November 1, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-28014 Filed 11-4-10; 8:45 am]
BILLING CODE 4160-01-P