Agency Information Collection Activities; Submission for Office of Management and Budget Review; 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, 17607-17609 [2021-06933]
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Federal Register / Vol. 86, No. 63 / Monday, April 5, 2021 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2021–0036; NIOSH 278]
Board of Scientific Counselors,
National Institute for Occupational
Safety and Health (BSC, NIOSH)
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of meeting and request
for comment.
AGENCY:
In accordance with the
Federal Advisory Committee Act, the
CDC announces the following virtual
meeting of the Board of Scientific
Counselors, National Institute for
Occupational Safety and Health (BSC,
NIOSH). This is a virtual meeting. It is
open to the public, limited only by web
conference lines (500 web conference
lines are available). If you wish to
attend, please register at the NIOSH
website https://www.cdc.gov/niosh/bsc/
or call (404–498–2581) no later than
May 12, 2021. Time will be available for
public comment.
DATES: The meeting will be held on May
19, 2021, from 10:00 a.m. to 4:00 p.m.,
EDT.
ADDRESSES: This is a virtual meeting.
You may submit comments, identified
by Docket No. CDC–2021–0036;
NIOSH–278 by mail. CDC does not
accept comments by email.
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Docket number CDC–2021–
0036; NIOSH–278, c/o Sherri Diana,
NIOSH Docket Office, National Institute
for Occupational Safety and Health,
1090 Tusculum Avenue, MS C–34,
Cincinnati, Ohio 45226.
Instructions: All submissions received
must include the Agency name and
Docket Number. Written public
comments received by May 12, 2021,
will be provided to the BSC prior to the
meeting. Docket number CDC–2021–
0036; NIOSH–278 will close May 12,
2021.
SUMMARY:
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FOR FURTHER INFORMATION CONTACT:
Emily J.K. Novicki, M.A., M.P.H.,
Executive Secretary, BSC, NIOSH, CDC,
1600 Clifton Avenue, MS V24–4,
Atlanta, Georgia 30329–4027,
Telephone (404) 498–2581, or email at
enovicki@cdc.gov.
SUPPLEMENTARY INFORMATION:
Purpose: The Secretary, the Assistant
Secretary for Health, and by delegation
the Director, Centers for Disease Control
VerDate Sep<11>2014
17:23 Apr 02, 2021
Jkt 253001
and Prevention, are authorized under
Sections 301 and 308 of the Public
Health Service Act to conduct directly
or by grants or contracts, research,
experiments, and demonstrations
relating to occupational safety and
health and to mine health. The Board of
Scientific Counselors provides guidance
to the Director, National Institute for
Occupational Safety and Health on
research and prevention programs.
Specifically, the Board provides
guidance on the Institute’s research
activities related to developing and
evaluating hypotheses, systematically
documenting findings and
disseminating results. The Board
evaluates the degree to which the
activities of the National Institute for
Occupational Safety and Health: (1)
Conform to appropriate scientific
standards, (2) address current, relevant
needs, and (3) produce intended results.
Matters To Be Considered: The agenda
for the meeting addresses work-related
fatigue, specifically the evolution of
workplace fatigue research; the NIOSH
Center for Work and Fatigue Research;
Emerging issues in workplace fatigue
and fatigue management in Agriculture,
Forestry and Fishing; Fatigue
Management: Technological advances
and Fatigue Risk Management Systems;
COVID–19 and workplace fatigue:
Lessons learned and mitigation
strategies; and Global perspectives on
workplace fatigue and fatigue risk
management.
An agenda is also posted on the
NIOSH website (https://www.cdc.gov/
niosh/bsc/).
Meeting Information: It is open to the
public, limited only by web conference
lines (500 web conference lines are
available). Register at the NIOSH
website https://www.cdc.gov/niosh/bsc/
or call (404–498–2581) no later than
May 12, 2021.
Public Participation
Comments received are part of the
public record and are subject to public
disclosure. Do not include any
information in your comment or
supporting materials that you consider
confidential or inappropriate for public
disclosure. If you include your name,
contact information, or other
information that identifies you in the
body of your comments, that
information will be on public display.
CDC will review all submissions and
may choose to redact, or withhold,
submissions containing private or
proprietary information such as Social
Security numbers, medical information,
inappropriate language, or duplicate/
near duplicate examples of a mass-mail
campaign. CDC will carefully consider
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Fmt 4703
Sfmt 4703
17607
all comments submitted into the docket.
CDC does not accept comment by email.
Oral Public Comment: The public is
welcome to participate during the
public comment period, from 3:00 p.m.
to 3:15 p.m., EDT, May 19, 2021. Please
note that the public comment period
ends at the time indicated above. Each
commenter will be provided up to five
minutes for comment. A limited number
of time slots are available and will be
assigned on a first come-first served
basis. Members of the public who wish
to address the BSC NIOSH are requested
to contact the Executive Secretary for
scheduling purposes (see FOR FUTHER
INFORMATION above).
Written Public Comment: Written
comments will also be accepted from
those unable to attend the public
session per the instructions provided in
the address section above. Written
comments received in advance of the
meeting will be included in the official
record of the meeting. Written
comments received by May 12, 2021,
will be provided to the BSC prior to the
meeting. Docket number CDC–2021–
0036; NIOSH–278 will close May 12,
2021.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2021–06927 Filed 4–2–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2017–N–6397]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
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:
E:\FR\FM\05APN1.SGM
Notice.
05APN1
17608
Federal Register / Vol. 86, No. 63 / Monday, April 5, 2021 / Notices
The Food and Drug
Administration (FDA or we) 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: Submit written comments
(including recommendations) on the
collection of information by May 5,
2021.
SUMMARY:
To ensure that comments on
the information collection are received,
OMB recommends that written
comments be submitted to https://
www.reginfo.gov/public/do/PRAMain.
Find this particular information
collection by selecting ‘‘Currently under
Review—Open for Public Comments’’ or
by using the search function. The OMB
control number for this information
collection is 0910–0782. Also include
the FDA docket number found in
brackets in the heading of this
document.
ADDRESSES:
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.
In
compliance with 44 U.S.C. 3507, FDA
SUPPLEMENTARY INFORMATION:
has submitted the following proposed
collection of information to OMB for
review and clearance.
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 (21 CFR 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.
In the Federal Register of December 4,
2020 (85 FR 78334), we published a 60day notice requesting public comment
on the proposed collection of
information. Although some general
comments were received regarding the
applicable labeling requirements, no
comments suggested we revise the
information collection burden we
estimate under 5 CFR 1320.5(a)(1)(B).
We estimate the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of
respondents
Number of
responses per
respondent
Total annual
responses
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
Total annual
records
Average
burden per
recordkeeping
Activity using Form FDA 3757; 21 CFR section
1 There
Average
burden per
response
Total hours
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 section
Initial Burden (Annualized over 3 years):
Initial Nutrition Analysis; 101.8(c)(2)(i)(A) ...........................................................
Annual Burden:
Recurring Nutrition Analysis; 101.8(c)(2)(i)(A) ....................................................
Total .............................................................................................................
jbell on DSKJLSW7X2PROD with NOTICES
1 There
Number of
records per
recordkeeper
Total hours
69,017
1
69,017
0.25 (15 minutes)
17,254
30,059
1
30,059
0.25 (15 minutes)
7,515
....................
........................
....................
...............................
24,769
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 3—ESTIMATED ANNUAL THIRD-PARTY DISCLOSURE BURDEN 1
Activity; 21 CFR section
Calorie Analysis; 101.8(c)(2)(i) ...................................................................................
Calorie Declaration Signage; 101.8(c)(2)(ii) ...............................................................
VerDate Sep<11>2014
17:23 Apr 02, 2021
Jkt 253001
PO 00000
Frm 00023
Fmt 4703
I
Number of
respondents
Number of
disclosures
per respondent
Total annual
disclosures
282
3,279
11
2,122
3,102
6,958,038
Sfmt 4703
I
I
E:\FR\FM\05APN1.SGM
05APN1
Average
burden per
disclosure
1 ...........................
0.21 (12.5 minutes).
I
Total hours
3,102
1,461,188
17609
Federal Register / Vol. 86, No. 63 / Monday, April 5, 2021 / Notices
TABLE 3—ESTIMATED ANNUAL THIRD-PARTY DISCLOSURE BURDEN 1—Continued
Number of
respondents
Number of
disclosures
per respondent
Total annual
disclosures
Average
burden per
disclosure
Vending Operator Contact Information; 101.8(e)(1) ..................................................
3,279
125
409,875
0.025 (1.5 minutes).
Total .............................................................................................................
....................
........................
....................
Activity; 21 CFR section
1 There
Dated: March 30, 2021.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[FR Doc. 2021–06933 Filed 4–2–21; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2020–N–1647]
Science Advisory Board to the
National Center for Toxicological
Research Advisory Committee; Notice
of Meeting
AGENCY:
Food and Drug Administration,
HHS.
Notice.
The Food and Drug
Administration (FDA) announces a
forthcoming virtual public advisory
committee meeting of the Science
Advisory Board to the National Center
for Toxicological Research. The general
function of the committee is to provide
advice and recommendations to the
Agency on research being conducted at
the National Center for Toxicological
Research (NCTR). At least one portion of
the meeting will be closed to the public.
DATES: The meeting will be held
virtually on May 11, 2021, from 8 a.m.
to 5:55 p.m., Central Standard Time,
and on May 12, 2021 from 8 a.m. to
11:30 a.m., Central Standard Time.
ADDRESSES: Please note that due to the
impact of this COVID–19 pandemic, all
meeting participants will be joining this
advisory committee meeting via an
online teleconferencing platform.
Answers to commonly asked questions
about FDA advisory committee meetings
may be accessed at: https://
www.fda.gov/advisory-committees/
about-advisory-committees/commonquestions-and-answers-about-fdaadvisory-committee-meetings. The
meeting will be webcast both days and
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
10,247
1,474,537
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.
ACTION:
...............................
Total hours
VerDate Sep<11>2014
17:23 Apr 02, 2021
Jkt 253001
will be available at the following link:
https://collaboration.fda.gov/nctr1000/.
FOR FURTHER INFORMATION CONTACT:
Donna Mendrick, National Center for
Toxicological Research, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 32, Rm. 2208, Silver Spring,
MD 20993–0002, 301–796–8892, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area). A notice in the
Federal Register about last minute
modifications that impact a previously
announced advisory committee meeting
cannot always be published quickly
enough to provide timely notice.
Therefore, you should always check the
Agency’s website at https://
www.fda.gov/advisory-committees and
scroll down to the appropriate advisory
committee meeting link, or call the
advisory committee information line to
learn about possible modifications
before joining the meeting.
SUPPLEMENTARY INFORMATION:
Agenda: On May 11, 2021, the
Science Advisory Board Chair will
welcome the participants, and the NCTR
Director will provide a Center-wide
update on scientific initiatives and
accomplishments during the past year.
The Science Advisory Board will be
presented with an overview of the
Science Advisory Board Subcommittee
Site Visit Report and a response to this
review. The Center for Biologics
Evaluation and Research, Center for
Drug Evaluation and Research, Center
for Devices and Radiological Health,
Center for Food Safety and Applied
Nutrition, Center for Tobacco Products,
and the Office of Regulatory Affairs will
each briefly discuss their specific
research strategic needs and potential
areas of collaboration.
On May 12, 2021, there will be
updates from the NCTR Research
Divisions and a public comment
session. Following an open discussion
of all the information presented, the
open session of the meeting will close
so the Science Advisory Board members
can discuss personnel issues at NCTR.
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
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Frm 00024
Fmt 4703
Sfmt 4703
material on its website prior to the
meeting, the background material will
be made publicly available at https://
collaboration.fda.gov/nctr1000/, and the
recording plus transcript will be posted
on FDA’s website after the meeting.
Background material is available at
https://www.fda.gov/advisorycommittees/advisory-committeecalendar. Scroll down to the
appropriate advisory committee meeting
link.
Procedure: On May 11, 2021, from 8
a.m. to 5:55 p.m., Central Standard
Time, and May 12, 2021, from 8 a.m. to
11:30 a.m., Central Standard Time, the
meeting is open to the public. Interested
persons may present data, information,
or views, orally or in writing, on issues
pending before the committee. Written
submissions may be made to the contact
person (see FOR FURTHER INFORMATION
CONTACT) on or before May 4, 2021. Oral
presentations from the public will be
scheduled between approximately 1
p.m. and 2 p.m. Central Standard Time.
Those individuals interested in making
formal oral presentations should notify
the contact person and submit a brief
statement of the general nature of the
evidence or arguments they wish to
present, the names and addresses of
proposed participants, and an
indication of the approximate time
requested to make their presentation on
or before April 26, 2021. Time allotted
for each presentation may be limited. If
the number of registrants requesting to
speak is greater than can be reasonably
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by April 27, 2021.
Closed Committee Deliberations: On
May 12, 2021, from 11:30 a.m. to 12
p.m., Central Standard Time, the
meeting will be closed to permit
discussion where disclosure would
constitute a clearly unwarranted
invasion of personal privacy (5 U.S.C.
552b(c)(6)). This portion of the meeting
will be closed to permit discussion of
information concerning individuals
E:\FR\FM\05APN1.SGM
05APN1
]]>Agencies
[Federal Register Volume 86, Number 63 (Monday, April 5, 2021)]
[Notices]
[Pages 17607-17609]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-06933]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2017-N-6397]
Agency Information Collection Activities; Submission for Office
of Management and Budget Review; 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.
-----------------------------------------------------------------------
[[Page 17608]]
SUMMARY: The Food and Drug Administration (FDA or we) 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: Submit written comments (including recommendations) on the
collection of information by May 5, 2021.
ADDRESSES: To ensure that comments on the information collection are
received, OMB recommends that written comments be submitted to https://www.reginfo.gov/public/do/PRAMain. Find this particular information
collection by selecting ``Currently under Review--Open for Public
Comments'' or by using the search function. The OMB control number for
this information collection is 0910-0782. Also include the FDA docket
number found in brackets in the heading of this document.
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: In compliance with 44 U.S.C. 3507, FDA has
submitted the following proposed collection of information to OMB for
review and clearance.
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
(21 CFR 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.
In the Federal Register of December 4, 2020 (85 FR 78334), we
published a 60-day notice requesting public comment on the proposed
collection of information. Although some general comments were received
regarding the applicable labeling requirements, no comments suggested
we revise the information collection burden we estimate under 5 CFR
1320.5(a)(1)(B).
We estimate the burden of this collection of information as
follows:
Table 1--Estimated Annual Reporting Burden \1\
----------------------------------------------------------------------------------------------------------------
Number of Total
Activity using Form FDA 3757; 21 Number of responses per annual Average burden per Total hours
CFR section respondents respondent responses response
----------------------------------------------------------------------------------------------------------------
Initial Registration for Vending 13 1 13 2...................... 26
Machine Labeling; 101.8(d).
Registration Renewal for Vending 19 1 19 0.5 (30 minutes)....... 9.5
Machine Labeling; 101.8(d).
Initial Registration for Menu 3,559 1 3,559 2...................... 7,118
Labeling; 101.11(d).
Registration Renewal for Menu 5,340 1 5,340 0.5 (30 minutes)....... 2,670
Labeling; 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 Total
Activity; 21 CFR section Number of records per annual Average burden per Total hours
recordkeepers recordkeeper records recordkeeping
----------------------------------------------------------------------------------------------------------------
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 30,059 1 30,059 0.25 (15 minutes)..... 7,515
Analysis;
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 Total
Activity; 21 CFR section Number of disclosures annual Average burden per Total hours
respondents per respondent disclosures disclosure
----------------------------------------------------------------------------------------------------------------
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).
[[Page 17609]]
Vending Operator Contact 3,279 125 409,875 0.025 (1.5 minutes).... 10,247
Information; 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: March 30, 2021.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2021-06933 Filed 4-2-21; 8:45 am]
BILLING CODE 4164-01-P
