Agency Information Collection Activities; Submission for Office of Management and Budget Review; 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, 5380-5384 [2011-1993]
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Federal Register / Vol. 76, No. 20 / Monday, January 31, 2011 / Notices
Dated: January 25, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2011–1998 Filed 1–28–11; 8:45 am]
BILLING CODE 4163–18–P
Dated: January 26, 2011.
Jill Hartzler Warner,
Acting Associate Commissioner for Special
Medical Programs.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2011–1992 Filed 1–28–11; 8:45 am]
Food and Drug Administration
BILLING CODE 4160–01–P
[Docket No. FDA 2011–N–0002]
Advisory Committees; Filing of Closed
Meeting Reports
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
The Food and Drug
Administration (FDA) is announcing
that, as required by the Federal
Advisory Committee Act, the Agency
has filed with the Library of Congress
the annual reports of those FDA
advisory committees that held closed
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ADDRESSES: Copies are available from
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SUMMARY:
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FOR FURTHER INFORMATION CONTACT:
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Officer, Advisory Committee and
Oversight Management Staff, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 32, rm. 5290,
Silver Spring, MD 20993–0002, 301–
796–8220.
SUPPLEMENTARY INFORMATION: Under
section 10(d) of the Federal Advisory
Committee Act (5 U.S.C. app.1) and 21
CFR 14.60(d), FDA has filed with the
Library of Congress the annual reports
for the following FDA advisory
committees that held closed meetings
during the period October 1, 2009,
through September 30, 2010:
Center for Biologics Evaluation and
Research:
Blood Products Advisory Committee,
Vaccines and Related Biological
Products Advisory Committee.
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Research:
Science Board to the National Center
for Toxicological Research.
Annual reports are available for
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4 p.m., Monday through Friday at the
following locations:
1. The Library of Congress, Madison
Bldg., Newspaper and Current
16:38 Jan 28, 2011
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0567]
Notice.
VerDate Mar<15>2010
Periodical Reading Room, 101
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2. The Division of Dockets
Management (HFA–305), Food and Drug
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Jkt 223001
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
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.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by March 2,
2011.
SUMMARY:
To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0665. Also
include the FDA docket number found
in brackets in the heading of this
document.
ADDRESSES:
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.
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
SUPPLEMENTARY INFORMATION:
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collection of information to OMB for
review and clearance.
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 Patient Protection
and Affordable Care Act of 2010
(‘‘Affordable Care Act’’) (Pub. L. 111–
148). Section 4205 of the legislation,
which principally amends sections 403
and 403A of the Federal Food, Drug,
and Cosmetic Act (the FD&C 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 of
the Affordable Care Act 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.
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Federal Register / Vol. 76, No. 20 / Monday, January 31, 2011 / Notices
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.
FDA published a second notice of
availability in the Federal Register of
August 25, 2010 (75 FR 52426),
announcing the availability of a draft
guidance document entitled ’’Draft
Guidance for Industry: Questions and
Answers Regarding Implementation of
the Menu Labeling Provisions of Section
4205 of the Patient Protection and
Affordable Care Act of 2010.’’ In the
Federal Register of January 25, 2011 (76
FR 4360), FDA announced the
withdrawal of this draft guidance and
its intention to complete the notice-andcomment rulemaking process for section
4205 before initiating enforcement
activities based, in part, on extensive
comments on the draft guidance
submitted to the Agency.
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 SRFE, 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
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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.
In accordance with 5 CFR 1320.8(d),
in the Federal Register of November 5,
2010 (75 FR 68361) (November 5, 2010
notice), FDA published a 60-day notice
requesting public comment on the
proposed collection of information. FDA
received 20 letters in response to the
notice, each containing 1 or more
comments.
(Comment 1) FDA received several
comments on the utility of the vending
machine labeling provisions of section
4205 of the Affordable Care Act. Some
comments argued that the Affordable
Care Act’s vending machine labeling
provisions have very little utility
because the consumer is already
familiar with the calorie content of
vending machine products. Other
comments stated that vending machine
labeling would be useful to the
consumer because grouping items in
vending machines into categories (e.g.,
beverages, chips, gums) on a menu
would help consumers select items by
comparing similar items.
(Response) As noted previously,
section 4205 of the Affordable Care Act
amends section 403(q) of the FD&C Act
to, among other things, require vending
machine operators that own or operate
20 or more vending machines to
disclose nutrient content for certain
food articles sold from vending
machines; thus, this requirement is
imposed by the law itself. Congress
required FDA to publish a proposed rule
by March 23, 2011, explaining how it
will implement the law. Comments such
as these on the utility of the provisions
of the law are being considered by FDA
in developing the proposed rules. FDA
will also accept comments on the
proposed rule and will consider them
fully in developing final rules.
(Comment 2) Several comments
suggested ways in which the burden of
disclosing calorie content of vending
machine products could be lessened.
One comment suggested that vendors be
permitted to post a sheet or menu on
vending machines that lists the caloric
contents of all their products. Another
comment proposed electronic posting of
calorie information, similar to the way
that some vending machines post prices
(the consumer looks it up by pressing
the item number before making a
purchase). Several other comments
suggested ways in which the burden of
disclosing calorie content on restaurant
menus could be lessened. For example,
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comments suggested that restaurants be
allowed flexibility with menu labeling
because of the many types of menus and
menu boards, citing the need for
different menus for full service vs. quick
service, drive-through service, carryout
orders, and self-service food or buffets.
Suggestions for flexibility included
permitting the calorie disclosures on
handouts or placards; permitting
disclosures to be brief, only required on
one page of the menu or one panel of
the menu board, and combined with
other required statements and
disclosures; permitting calorie
disclosure for self-service beverages on
the menu board as opposed to at the
beverage fountain; and permitting a
standard per ounce calorie disclosure
for standardized beverages such as
coffee and orange juice.
(Response) The requirement that
affected chain retail food establishments
and vending machine operators disclose
certain nutrition information for certain
food items offered for sale is imposed by
section 4205 of the Affordable Care Act.
Comments such as these on minimizing
the burden of the law are being
considered by FDA in developing the
proposed rule. FDA will also accept
comments on the proposed rules and
will consider them fully in developing
final rules.
(Comment 3) Several comments
argued that FDA underestimated the
burden hours and costs associated with
complying with the provisions of
section 4205 of the Affordable Care Act.
Several comments argued that the
annual burden hours will be higher than
FDA’s estimate. One comment argued
that FDA did not fully consider the time
needed to acquire the required nutrition
information. One comment suggested
that FDA provide estimated burden
hours individualized for each industry
(i.e., convenience stores, restaurants,
and grocery stores). Some comments
argued that FDA underestimated the
number of affected businesses in the
United States and their rate of growth.
Other comments argued that the
percentages of the industries that will be
impacted will be higher.
(Response) FDA appreciates the data
and suggestions provided in the
comments. However, the Agency stands
by its preliminary estimate of the
paperwork burden resulting from
section 4205 of the Affordable Care Act.
Thus, FDA has not changed the burden
hour estimates in tables 1 and 2 of this
document. This rough estimate of 14
million recurring hours in annual
burden was a preliminary figure
designed to cover a range of possible,
non-specific requirements. During the
upcoming rulemaking process, FDA
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seeks to minimize the regulatory burden
on small businesses, and we anticipate
the actual burden may differ from the
preliminary estimate, depending upon
the specific requirements that will be
laid out in the final rules.
(Comment 4) Several comments had
suggestions for the upcoming
rulemaking.
(Response) FDA appreciates the
information provided in the comments
and will consider them in the upcoming
rulemakings.
(Comment 5) One comment identified
our inadvertent omission of the capital
costs column in table 2 of the November
5, 2010 notice.
(Response) We have corrected the
table in this document by inserting the
missing capital costs column for
comment.
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 the following
tables in order to annualize the burden
hours over a 3-year period, yielding
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, that 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
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 1 of 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.
TABLE 1—ESTIMATED ANNUAL RECORDKEEPING BURDEN: CALORIE ANALYSIS AND RECORDING 1
117
40
60,372
22,800
4
4
241,488
91,200
$16.2 million.
$6.1 million.
420
600
40
20
16,800
12,000
4
2
1,506
30
3
4
60
20
6,024
1,800
60
4
4
2
67,200
24,000
423,888
24,096
7,200
120
31,416
$4.5 million.
$20,000.
$26.9 million.
$1.6 million.
$0.5 million.
$4,000.
$2.1 million.
Hours per
record
Total hours
Total capital costs
are no operating and maintenance costs associated with this collection of information.
Third Party Disclosure Burdens for
Chain Retail Food Establishments
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Total annual
records
516
570
Restaurant chains ..........................
Grocery and Convenience Store
chains.
Other chains ..................................
Vending operators .........................
Total initial hours ...........................
New/Reformulated items ...............
New chains ....................................
New vendors ..................................
Total recurring hours ..............
1 There
Annual frequency
per
recordkeeping
Number of
recordkeepers
Type of respondent
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.
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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
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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).
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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.
The estimated capital cost for Other
chains decreased from $22 million to
$18.2 million because of an arithmetic
error. Correcting this error caused the
Total initial capital costs to fall from
$269.1 million to $265.3 million. A
rounding error in the capital costs for
’’New SRFE outlets’’ led to an increase
in estimated costs from $0.6 million to
$0.7 million. Correcting this error led to
an increase in the Total recurring capital
costs of $0.1 million, to $3.5 million.
TABLE 2—ESTIMATED ANNUAL THIRD PARTY DISCLOSURE BURDEN: CALORIE CONTENT 1
Number of
respondents
Type of respondent
Restaurants ..............................................
Grocery and Convenience Store chains ..
Other chains .............................................
Total initial hours ..............................
New SRFE outlets ...................................
Vending (ongoing) ....................................
Vending (growth) ......................................
Total recurring hours ........................
1 There
Total annual
disclosures
Hours per
disclosure
Total hours
135,705
41,945
33,114
3
1
1
407,115
41,945
33,114
2
2
2
600
5,000
5,000
2
56,000
140
1,200
280,000,000
700,000
2
0.05
0.05
814,230
83,890
66,228
964,348
2,400
14,000,000
35,000
14,037,400
Total capital
costs
$224
$23.1
$18.2
$265.3
0.7
$2.8
million.
million.
million.
million.
million.
million.
$7,000.
$3.5 million.
are no operating and maintenance costs associated with this collection of information.
Burdens for Chain Vending Machine
Operators
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Annual
frequency of
disclosure
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
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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 below. 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 × 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 the
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 likely will 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
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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.
Because stickers do not require any
initial investment and because they are
not durable, all burden and costs will be
on a recurring basis. 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,
two 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
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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 ( =
5,000 firms × 1,400 machines/firm × 20
displays/machine × .05 hours/display ×
2). This amount is recurring in every
year, and is given in row 7 of table 2 of
the 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
( = 5,000 firms × 7 machines/firm × 20
items/machine × .05 hours/item). This
amount is displayed in row 8 of table 2
of this document.
Dated: January 25, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2011–1993 Filed 1–28–11; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0564]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Restaurant Menu
and Vending Machine Labeling:
Registration for Small Chains Under
Section 4205 of the Patient Protection
and Affordable Care Act of 2010
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by March 2,
2011.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
jlentini on DSKJ8SOYB1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
16:38 Jan 28, 2011
Jkt 223001
202–395–7285, or emailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0664. Also
include the FDA 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: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
I. Background
Restaurant Menu and Vending
Machine Labeling: Registration for
Small Chains Under Section 4205 of the
Patient Protection and Affordable Care
Act of 2010—(OMB Control Number
0910–0664)—Revision.
On March 23, 2010, the President
signed into law the Patient Protection
and Affordable Care Act of 2010
(Affordable Care Act) (Pub. L. 111–148).
Section 4205 of the legislation, which
principally amends sections 403 and
403A of the Federal Food, Drug, and
Cosmetic Act (the FD&C Act) (21 U.S.C.
343 and 343–1, respectively), requires
chain restaurants and similar retail food
establishments (SRFE) with 20 or more
locations, as well as operators of 20 or
more vending machines, to disclose
certain nutrition information on 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 in restaurants and
calorie declarations for food in vending
machines that are not ‘‘identical to’’ the
section 4205 requirements.
In addition to restaurant menu and
vending machine labeling, section 4205
of the Affordable Care Act provides that
persons or firms not subject to the
disclosure of nutrition information
required by this legislation, such as
restaurants with fewer than 20 locations
or vending machine operators with
fewer than 20 vending machines, may
elect to be subject to the requirements
provided in section 4205 by registering
biannually with FDA. As required by
section 4205, FDA published a notice in
the Federal Register of July 23, 2010 (75
FR 43182) (the July 23, 2010, notice) to
explain how retail food establishments
and vending machine operators not
otherwise subject to the provisions of
section 4205 may voluntarily elect to
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
become subject to them. The
information collection requirements of
FDA’s program of voluntary registration
under section 4205 of the Affordable
Care Act were approved under OMB
control number 0910–0664.
Voluntary registration allows
companies with outlets or machines
regulated by local or State calorie
labeling requirements to opt instead for
the requirements of section 4205 of the
Affordable Care Act. The information
provided to FDA will help Federal,
State or local officials to determine
which jurisdiction’s requirements apply
to the firm.
Description of Respondents:
Respondents to this collection of
information include retail food
establishments and vending machine
operators with fewer than 20 outlets or
machines.
FDA’s July 23, 2010, notice requires
that retail food establishments and
vending machine operators register with
FDA using the Agency’s Form FDA 3757
available at https://www.fda.gov/
menulabeling. FDA prefers that the
information be submitted by email by
typing complete information into the
form (PDF), saving it on the registrant’s
computer, and sending it by email to
https://
menulawregistration@fda.hhs.gov. If
email is not available, the registrant can
either fill in the form (PDF) and print it
out (or print out the blank PDF and fill
in the information by hand or
typewriter), and send it to FDA either by
faxing the completed form to 301–436–
2804 or mailing it to the Center for Food
Safety and Applied Nutrition,
Compliance Information Branch (HFS–
681), 5600 Fishers Lane, Rockville, MD
20857.
Information FDA requires on the
registration form for restaurants and
similar retail food establishments
includes the following:
• The name, address, phone number,
email address, and contact information
for the authorized official;
• The name, address, and email
address of each restaurant or similar
retail food establishment being
registered, as well as the name and
contact information for an official
onsite, such as the owner or manager,
for each specific restaurant or similar
retail food establishment;
• All trade names the restaurant or
similar retail food establishment uses;
• Preferred mailing address (if
different from location address for each
establishment) for purposes of receiving
correspondence; and
• Certification that the information
submitted is true and accurate, that the
person or firm submitting it is
E:\FR\FM\31JAN1.SGM
31JAN1
Agencies
[Federal Register Volume 76, Number 20 (Monday, January 31, 2011)]
[Notices]
[Pages 5380-5384]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-1993]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0567]
Agency Information Collection Activities; Submission for Office
of Management and Budget Review; 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 that a
proposed collection of information has been submitted to the Office of
Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Fax written comments on the collection of information by March
2, 2011.
ADDRESSES: To ensure that comments on the information collection are
received, OMB recommends that written comments be faxed to the Office
of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer,
FAX: 202-395-7285, or e-mailed to oira_submission@omb.eop.gov. All
comments should be identified with the OMB control number 0910-0665.
Also include the FDA 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: In compliance with 44 U.S.C. 3507, FDA has
submitted the following proposed collection of information to OMB for
review and clearance.
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 Patient
Protection and Affordable Care Act of 2010 (``Affordable Care Act'')
(Pub. L. 111-148). Section 4205 of the legislation, which principally
amends sections 403 and 403A of the Federal Food, Drug, and Cosmetic
Act (the FD&C 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 of the Affordable Care Act 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.
[[Page 5381]]
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.
FDA published a second notice of availability in the Federal
Register of August 25, 2010 (75 FR 52426), announcing the availability
of a draft guidance document entitled ''Draft Guidance for Industry:
Questions and Answers Regarding Implementation of the Menu Labeling
Provisions of Section 4205 of the Patient Protection and Affordable
Care Act of 2010.'' In the Federal Register of January 25, 2011 (76 FR
4360), FDA announced the withdrawal of this draft guidance and its
intention to complete the notice-and-comment rulemaking process for
section 4205 before initiating enforcement activities based, in part,
on extensive comments on the draft guidance submitted to the Agency.
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 SRFE, 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.
In accordance with 5 CFR 1320.8(d), in the Federal Register of
November 5, 2010 (75 FR 68361) (November 5, 2010 notice), FDA published
a 60-day notice requesting public comment on the proposed collection of
information. FDA received 20 letters in response to the notice, each
containing 1 or more comments.
(Comment 1) FDA received several comments on the utility of the
vending machine labeling provisions of section 4205 of the Affordable
Care Act. Some comments argued that the Affordable Care Act's vending
machine labeling provisions have very little utility because the
consumer is already familiar with the calorie content of vending
machine products. Other comments stated that vending machine labeling
would be useful to the consumer because grouping items in vending
machines into categories (e.g., beverages, chips, gums) on a menu would
help consumers select items by comparing similar items.
(Response) As noted previously, section 4205 of the Affordable Care
Act amends section 403(q) of the FD&C Act to, among other things,
require vending machine operators that own or operate 20 or more
vending machines to disclose nutrient content for certain food articles
sold from vending machines; thus, this requirement is imposed by the
law itself. Congress required FDA to publish a proposed rule by March
23, 2011, explaining how it will implement the law. Comments such as
these on the utility of the provisions of the law are being considered
by FDA in developing the proposed rules. FDA will also accept comments
on the proposed rule and will consider them fully in developing final
rules.
(Comment 2) Several comments suggested ways in which the burden of
disclosing calorie content of vending machine products could be
lessened. One comment suggested that vendors be permitted to post a
sheet or menu on vending machines that lists the caloric contents of
all their products. Another comment proposed electronic posting of
calorie information, similar to the way that some vending machines post
prices (the consumer looks it up by pressing the item number before
making a purchase). Several other comments suggested ways in which the
burden of disclosing calorie content on restaurant menus could be
lessened. For example, comments suggested that restaurants be allowed
flexibility with menu labeling because of the many types of menus and
menu boards, citing the need for different menus for full service vs.
quick service, drive-through service, carryout orders, and self-service
food or buffets. Suggestions for flexibility included permitting the
calorie disclosures on handouts or placards; permitting disclosures to
be brief, only required on one page of the menu or one panel of the
menu board, and combined with other required statements and
disclosures; permitting calorie disclosure for self-service beverages
on the menu board as opposed to at the beverage fountain; and
permitting a standard per ounce calorie disclosure for standardized
beverages such as coffee and orange juice.
(Response) The requirement that affected chain retail food
establishments and vending machine operators disclose certain nutrition
information for certain food items offered for sale is imposed by
section 4205 of the Affordable Care Act. Comments such as these on
minimizing the burden of the law are being considered by FDA in
developing the proposed rule. FDA will also accept comments on the
proposed rules and will consider them fully in developing final rules.
(Comment 3) Several comments argued that FDA underestimated the
burden hours and costs associated with complying with the provisions of
section 4205 of the Affordable Care Act. Several comments argued that
the annual burden hours will be higher than FDA's estimate. One comment
argued that FDA did not fully consider the time needed to acquire the
required nutrition information. One comment suggested that FDA provide
estimated burden hours individualized for each industry (i.e.,
convenience stores, restaurants, and grocery stores). Some comments
argued that FDA underestimated the number of affected businesses in the
United States and their rate of growth. Other comments argued that the
percentages of the industries that will be impacted will be higher.
(Response) FDA appreciates the data and suggestions provided in the
comments. However, the Agency stands by its preliminary estimate of the
paperwork burden resulting from section 4205 of the Affordable Care
Act. Thus, FDA has not changed the burden hour estimates in tables 1
and 2 of this document. This rough estimate of 14 million recurring
hours in annual burden was a preliminary figure designed to cover a
range of possible, non-specific requirements. During the upcoming
rulemaking process, FDA
[[Page 5382]]
seeks to minimize the regulatory burden on small businesses, and we
anticipate the actual burden may differ from the preliminary estimate,
depending upon the specific requirements that will be laid out in the
final rules.
(Comment 4) Several comments had suggestions for the upcoming
rulemaking.
(Response) FDA appreciates the information provided in the comments
and will consider them in the upcoming rulemakings.
(Comment 5) One comment identified our inadvertent omission of the
capital costs column in table 2 of the November 5, 2010 notice.
(Response) We have corrected the table in this document by
inserting the missing capital costs column for comment.
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 the following tables in order
to annualize the burden hours over a 3-year period, yielding 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, that 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 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 1 of 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.
Table 1--Estimated Annual Recordkeeping Burden: Calorie Analysis and Recording \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Annual frequency Total
Type of respondent Number of per annual Hours per Total hours Total capital costs
recordkeepers recordkeeping 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 $20,000.
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 $2.1 million.
--------------------------------------------------------------------------------------------------------------------------------------------------------
\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).
[[Page 5383]]
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.
The estimated capital cost for Other chains decreased from $22
million to $18.2 million because of an arithmetic error. Correcting
this error caused the Total initial capital costs to fall from $269.1
million to $265.3 million. A rounding error in the capital costs for
''New SRFE outlets'' led to an increase in estimated costs from $0.6
million to $0.7 million. Correcting this error led to an increase in
the Total recurring capital costs of $0.1 million, to $3.5 million.
Table 2--Estimated Annual Third Party Disclosure Burden: Calorie Content \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Annual
Type of respondent Number of frequency of Total annual Hours per Total hours Total capital
respondents disclosure disclosures disclosure costs
--------------------------------------------------------------------------------------------------------------------------------------------------------
Restaurants............................................. 135,705 3 407,115 2 814,230 $224 million.
Grocery and Convenience Store chains.................... 41,945 1 41,945 2 83,890 $23.1 million.
Other chains............................................ 33,114 1 33,114 2 66,228 $18.2 million.
Total initial hours................................. .............. .............. .............. .............. 964,348 $265.3
million.
New SRFE outlets........................................ 600 2 1,200 2 2,400 0.7 million.
Vending (ongoing)....................................... 5,000 56,000 280,000,000 0.05 14,000,000 $2.8 million.
Vending (growth)........................................ 5,000 140 700,000 0.05 35,000 $7,000.
Total recurring hours............................... .............. .............. .............. .............. 14,037,400 $3.5 million.
--------------------------------------------------------------------------------------------------------------------------------------------------------
\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 below. 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 the 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 likely will 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. Because stickers do not require any initial investment
and because they are not durable, all burden and costs will be on a
recurring basis. 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, two 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
[[Page 5384]]
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 ( = 5,000 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 the 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 ( =
5,000 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: January 25, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2011-1993 Filed 1-28-11; 8:45 am]
BILLING CODE 4160-01-P