Agency Information Collection Activities; Proposed Collection; Comment Request; Food Labeling; Calorie Labeling of Articles of Food in Vending Machines and Nutrition Labeling of Standard Menu Items in Restaurants and Similar Retail Food Establishments, 78334-78336 [2020-26695]
Download as PDF
<![CDATA[
78334
Federal Register / Vol. 85, No. 234 / Friday, December 4, 2020 / Notices
65 or reach the 25th month of disability
benefit entitlement. These individuals
do not file a separate application for
Medicare Part A because their
application for Social Security or RRB
benefits is also an application for Part A.
The form is for individuals who are not
eligible for Social Security for RRB
benefits, but may qualify for premiumfree Medicare Part A based on certain
requirements outlined in § 406.11 and
406.15 or for certain disabled
individuals who may enroll in premium
Medicare Part A based on certain
requirements outlined in § 406.20.
Individuals may also choose to enroll in
Medicare Part B at the same time they
apply for Medicare Part A.
The Application for Enrollment in
Medicare Part A (CMS–18F5 and CMS–
18F5–SP) was designed to capture all
the information needed to make a
determination of an individual’s
entitlement to Part A. This Information
Collection Request (ICR) adds the
collection instruments SSA uses to
collect information from individuals
who are filing an Application for
Hospital Insurance, updates the burden
information. CMS will begin reporting
for additional collection instruments,
including the internet Claim System
(iClaim), Modernized Claims System
(MCS), and the Consolidated Claims
Experience (CCE). Form Number: CMS–
18F5 (OMB control number: 0938–
0251); Frequency: Annually; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
1,394,264; Total Annual Responses:
1,394,264; Total Annual Hours: 348,566.
(For policy questions regarding this
collection contact Carla Patterson at
410–786–1000.)
Dated: December 1, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2020–26756 Filed 12–3–20; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2017–N–6397]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Food Labeling;
Calorie Labeling of Articles of Food in
Vending Machines and Nutrition
Labeling of Standard Menu Items in
Restaurants and Similar Retail Food
Establishments
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
Under the Paperwork Reduction Act of
1995 (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 information
collection provisions for calorie labeling
of articles of food in vending machines
and nutrition labeling of standard menu
items in restaurants and similar retail
food establishments.
DATES: Submit either electronic or
written comments on the collection of
information by February 2, 2021.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before February 2,
2021. The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of February 2, 2021.
Comments received by mail/hand
delivery/courier (for written/paper
submissions) will be considered timely
if they are postmarked or the delivery
service acceptance receipt is on or
before that date.
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
VerDate Sep<11>2014
18:18 Dec 03, 2020
Jkt 253001
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2017–N–6397 for ‘‘Agency Information
Collection Activities; Proposed
Collection; Comment Request; Food
Labeling; Calorie Labeling of Articles of
Food in Vending Machines and
Nutrition Labeling of Standard Menu
Items in Restaurants and Similar Retail
Food Establishments.’’ Received
comments, those filed in a timely
manner (see ADDRESSES), will be placed
in the docket and, except for those
submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday, 240–402–7500.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
E:\FR\FM\04DEN1.SGM
04DEN1
Federal Register / Vol. 85, No. 234 / Friday, December 4, 2020 / Notices
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852, 240–402–7500.
FOR FURTHER INFORMATION CONTACT:
Domini Bean, Office of Operations,
Food and Drug Administration, Three
White Flint North, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–5733, PRAStaff@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3521), 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
VerDate Sep<11>2014
18:18 Dec 03, 2020
Jkt 253001
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests
or 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.
Food Labeling; Calorie Labeling of
Articles of Food in Vending Machines
and Nutrition Labeling of Standard
Menu Items in Restaurants and Similar
Retail Food Establishments
OMB Control Number 0910–0782—
Extension
This information collection supports
FDA regulations under part 101 (21 CFR
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
78335
part 101) and the associated collection
instrument Form FDA 3757. The
Federal Food, Drug, and Cosmetic Act
requires the disclosure of certain calorie
labeling of articles of food in vending
machines, as well as nutrition
information for standard menu items in
certain restaurants and retail food
establishments. Sections 101.8 and
101.11 provides that respondents with a
chain of 20 or more locations will
disclose nutritional information of
certain foods for consumers of food
products for the purpose of making
informed dietary choices. We also offer
registration for respondents who wish to
voluntarily participate with this
information collection activity, for
which we developed Form FDA 3757
entitled, ‘‘DHHS/FDA Menu and
Vending Machine Labeling Voluntary
Registration’’ to assist respondents in
this regard. To keep the registration
active, a respondent renews their
registration every other year within 60
days prior to the expiration of the
respondent’s current registration with
FDA, or it will automatically expire.
We use the collection of information
to help determine compliance with
regulatory requirements. Third-party
disclosure requirements are used by
consumers of food products for the
purpose of making informed dietary
choices.
Description of Respondents:
Respondents to this collection of
information are vending machine
operators and restaurants or other
similar food establishments that are
subject to the requirements of part 101
as well as those entities that voluntarily
participate with the provisions of this
collection of information.
E:\FR\FM\04DEN1.SGM
04DEN1
78336
Federal Register / Vol. 85, No. 234 / Friday, December 4, 2020 / Notices
We estimate the burden of the
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of
responses per
respondent
Number of
respondents
Activity using form FDA 3757; 21 CFR
Average burden
per response
(in hours)
Total annual
responses
Total hours
Initial Registration for Vending Machine Labeling; 101.8(d) .................
Registration Renewal for Vending Machine Labeling; 101.8(d) ...........
Initial Registration for Menu Labeling; 101.11(d) ..................................
Registration Renewal for Menu Labeling; 101.11(d) ............................
13
19
3,559
5,340
1
1
1
1
13
19
3,559
5,340
2 .....................................
0.5 (30 minutes) ............
2 .....................................
0.5 (30 minutes) ............
26
9.5
7,118
2,670
Total ...............................................................................................
........................
........................
........................
........................................
9,823.5
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 2—ESTIMATED RECORDKEEPING BURDEN 1
Number of
recordkeepers
Activity; 21 CFR
Number of
records per
recordkeeper
Average burden
per record
(in hours)
Total annual
records
Total hours
Initial Burden (Annualized over 3 years)
Initial Nutrition Analysis; 101.8(c)(2)(i)(A) .............................................
69,017
1
69,017
0.25 (15 minutes) ..........
17,254
Annual Burden
Recurring Nutrition Analysis; 101.8(c)(2)(i)(A) ......................................
30,059
1
30,059
0.25 (15 minutes) ..........
7,515
Total ...............................................................................................
........................
........................
........................
........................................
24,769
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 3—ESTIMATED ANNUAL THIRD-PARTY DISCLOSURE BURDEN 1
Number of
respondents
Activity; 21 CFR
Number of
disclosures per
respondent
Average burden
per disclosure
(in hours)
Total annual
disclosures
Total hours
Calorie Analysis; 101.8(c)(2)(i) .......................................................
Calorie Declaration Signage; 101.8(c)(2)(ii) ...................................
Vending Operator Contact Information; 101.8(e)(1) .......................
282
3,279
3,279
11
2,122
125
3,102
6,958,038
409,875
1 .....................................
0.21 (12.5 minutes) .......
0.025 (1.5 minutes) .......
3,102
1,461,188
10,247
Total .........................................................................................
........................
..............................
........................
........................................
1,474,537
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
Based on a review of the information
collection since our last request for
OMB approval, we have made no
adjustments to our burden estimate.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: November 30, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[Docket No. FDA–2017–D–5739]
[FR Doc. 2020–26695 Filed 12–3–20; 8:45 am]
BILLING CODE 4164–01–P
Food and Drug Administration
Formal Meetings Between the Food
and Drug Administration and
Abbreviated New Drug Application
Applicants of Complex Products Under
Generic Drug User Fee Amendments;
Guidance for Industry; Availability;
Correction
AGENCY:
Food and Drug Administration,
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
correcting a notice entitled ‘‘Formal
Meetings Between the Food and Drug
Administration and Abbreviated New
Drug Application Applicants of
Complex Products Under Generic Drug
User Fee Amendments; Guidance for
Industry; Availability’’ that appeared in
the Federal Register of November 25,
SUMMARY:
VerDate Sep<11>2014
18:18 Dec 03, 2020
Jkt 253001
PO 00000
In the
Federal Register of November 25, 2020
(85 FR 75336), in FR Doc. 2020–26050,
the following correction is made:
On page 75337, in the third column,
under the heading, ‘‘II. Paperwork
Reduction Act of 1995’’, the paragraph
is corrected to read:
‘‘While this guidance contains no
collection of information, it does refer to
previously approved FDA collections of
information. Therefore, clearance by the
Office of Management and Budget
SUPPLEMENTARY INFORMATION:
HHS.
ACTION:
2020. The document announced the
availability for a guidance for industry.
The document was published with
incorrect information in the Paperwork
Reduction Act of 1995 section. This
document corrects that error.
FOR FURTHER INFORMATION CONTACT:
Elizabeth Giaquinto Friedman, Center
for Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 75, Rm. 1670,
Silver Spring, MD 20993–0002, 240–
402–7930, elizabeth.giaquinto@
fda.hhs.gov.
Frm 00035
Fmt 4703
Sfmt 4703
E:\FR\FM\04DEN1.SGM
04DEN1
]]>Agencies
[Federal Register Volume 85, Number 234 (Friday, December 4, 2020)]
[Notices]
[Pages 78334-78336]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-26695]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2017-N-6397]
Agency Information Collection Activities; Proposed Collection;
Comment Request; Food Labeling; Calorie Labeling of Articles of Food in
Vending Machines and Nutrition Labeling of Standard Menu Items in
Restaurants and Similar Retail Food Establishments
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or Agency) is announcing
an opportunity for public comment on the proposed collection of certain
information by the Agency. Under the Paperwork Reduction Act of 1995
(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 information collection provisions for
calorie labeling of articles of food in vending machines and nutrition
labeling of standard menu items in restaurants and similar retail food
establishments.
DATES: Submit either electronic or written comments on the collection
of information by February 2, 2021.
ADDRESSES: You may submit comments as follows. Please note that late,
untimely filed comments will not be considered. Electronic comments
must be submitted on or before February 2, 2021. The https://www.regulations.gov electronic filing system will accept comments until
11:59 p.m. Eastern Time at the end of February 2, 2021. Comments
received by mail/hand delivery/courier (for written/paper submissions)
will be considered timely if they are postmarked or the delivery
service acceptance receipt is on or before that date.
Electronic Submissions
Submit electronic comments in the following way:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments. Comments submitted
electronically, including attachments, to https://www.regulations.gov
will be posted to the docket unchanged. Because your comment will be
made public, you are solely responsible for ensuring that your comment
does not include any confidential information that you or a third party
may not wish to be posted, such as medical information, your or anyone
else's Social Security number, or confidential business information,
such as a manufacturing process. Please note that if you include your
name, contact information, or other information that identifies you in
the body of your comments, that information will be posted on https://www.regulations.gov.
If you want to submit a comment with confidential
information that you do not wish to be made available to the public,
submit the comment as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').
Written/Paper Submissions
Submit written/paper submissions as follows:
Mail/Hand Delivery/Courier (for written/paper
submissions): Dockets Management Staff (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper comments submitted to the Dockets
Management Staff, FDA will post your comment, as well as any
attachments, except for information submitted, marked and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All submissions received must include the Docket No.
FDA-2017-N-6397 for ``Agency Information Collection Activities;
Proposed Collection; Comment Request; Food Labeling; Calorie Labeling
of Articles of Food in Vending Machines and Nutrition Labeling of
Standard Menu Items in Restaurants and Similar Retail Food
Establishments.'' Received comments, those filed in a timely manner
(see ADDRESSES), will be placed in the docket and, except for those
submitted as ``Confidential Submissions,'' publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m.
and 4 p.m., Monday through Friday, 240-402-7500.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your comments only as a written/paper submission. You
should submit two copies total. One copy will include the information
you claim to be confidential with a heading or cover note that states
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will
review this copy, including the claimed confidential information, in
its consideration of comments. The
[[Page 78335]]
second copy, which will have the claimed confidential information
redacted/blacked out, will be available for public viewing and posted
on https://www.regulations.gov. Submit both copies to the Dockets
Management Staff. If you do not wish your name and contact information
to be made publicly available, you can provide this information on the
cover sheet and not in the body of your comments and you must identify
this information as ``confidential.'' Any information marked as
``confidential'' will not be disclosed except in accordance with 21 CFR
10.20 and other applicable disclosure law. For more information about
FDA's posting of comments to public dockets, see 80 FR 56469, September
18, 2015, or access the information at: https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
Docket: For access to the docket to read background documents or
the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in
the heading of this document, into the ``Search'' box and follow the
prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane,
Rm. 1061, Rockville, MD 20852, 240-402-7500.
FOR FURTHER INFORMATION CONTACT: Domini Bean, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A-12M, 11601
Landsdown St., North Bethesda, MD 20852, 301-796-5733,
[email protected].
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3521), 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 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.
Food Labeling; Calorie Labeling of Articles of Food in Vending Machines
and Nutrition Labeling of Standard Menu Items in Restaurants and
Similar Retail Food Establishments
OMB Control Number 0910-0782--Extension
This information collection supports FDA regulations under part 101
(21 CFR part 101) and the associated collection instrument Form FDA
3757. The Federal Food, Drug, and Cosmetic Act requires the disclosure
of certain calorie labeling of articles of food in vending machines, as
well as nutrition information for standard menu items in certain
restaurants and retail food establishments. Sections 101.8 and 101.11
provides that respondents with a chain of 20 or more locations will
disclose nutritional information of certain foods for consumers of food
products for the purpose of making informed dietary choices. We also
offer registration for respondents who wish to voluntarily participate
with this information collection activity, for which we developed Form
FDA 3757 entitled, ``DHHS/FDA Menu and Vending Machine Labeling
Voluntary Registration'' to assist respondents in this regard. To keep
the registration active, a respondent renews their registration every
other year within 60 days prior to the expiration of the respondent's
current registration with FDA, or it will automatically expire.
We use the collection of information to help determine compliance
with regulatory requirements. Third-party disclosure requirements are
used by consumers of food products for the purpose of making informed
dietary choices.
Description of Respondents: Respondents to this collection of
information are vending machine operators and restaurants or other
similar food establishments that are subject to the requirements of
part 101 as well as those entities that voluntarily participate with
the provisions of this collection of information.
[[Page 78336]]
We estimate the burden of the collection of information as follows:
Table 1--Estimated Annual Reporting Burden \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
Activity using form FDA 3757; 21 CFR Number of responses per Total annual Average burden per response (in hours) Total hours
respondents respondent responses
--------------------------------------------------------------------------------------------------------------------------------------------------------
Initial Registration for Vending Machine 13 1 13 2......................................... 26
Labeling; 101.8(d).
Registration Renewal for Vending Machine 19 1 19 0.5 (30 minutes).......................... 9.5
Labeling; 101.8(d).
Initial Registration for Menu Labeling; 3,559 1 3,559 2......................................... 7,118
101.11(d).
Registration Renewal for Menu Labeling; 5,340 1 5,340 0.5 (30 minutes).......................... 2,670
101.11(d).
-----------------------------------------------------------------------------------------------------------
Total................................... .............. .............. .............. .......................................... 9,823.5
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
Table 2--Estimated Recordkeeping Burden \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
Activity; 21 CFR Number of records per Total annual Average burden per record (in hours) Total hours
recordkeepers recordkeeper records
--------------------------------------------------------------------------------------------------------------------------------------------------------
Initial Burden (Annualized over 3 years)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Initial Nutrition Analysis; 69,017 1 69,017 0.25 (15 minutes)......................... 17,254
101.8(c)(2)(i)(A).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Annual Burden
--------------------------------------------------------------------------------------------------------------------------------------------------------
Recurring Nutrition Analysis; 30,059 1 30,059 0.25 (15 minutes)......................... 7,515
101.8(c)(2)(i)(A).
-----------------------------------------------------------------------------------------------------------
Total................................... .............. .............. .............. .......................................... 24,769
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
Table 3--Estimated Annual Third-Party Disclosure Burden \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
Activity; 21 CFR Number of disclosures per Total annual Average burden per disclosure (in Total hours
respondents respondent disclosures hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Calorie Analysis; 101.8(c)(2)(i)........... 282 11 3,102 1....................................... 3,102
Calorie Declaration Signage; 3,279 2,122 6,958,038 0.21 (12.5 minutes)..................... 1,461,188
101.8(c)(2)(ii).
Vending Operator Contact Information; 3,279 125 409,875 0.025 (1.5 minutes)..................... 10,247
101.8(e)(1).
------------------------------------------------------------------------------------------------------------
Total.................................. .............. ................. .............. ........................................ 1,474,537
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
Based on a review of the information collection since our last
request for OMB approval, we have made no adjustments to our burden
estimate.
Dated: November 30, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2020-26695 Filed 12-3-20; 8:45 am]
BILLING CODE 4164-01-P
