Uniform Compliance Date for Food Labeling Regulations, 106996-106998 [2024-31419]
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106996
Federal Register / Vol. 89, No. 250 / Tuesday, December 31, 2024 / Rules and Regulations
pass or fail. The reviewer must be
afforded the same access to the premises
previously afforded to the auditor, if
requested.
(4) If the producer disagrees with the
final audit determination, the producer
may send a request for reconsideration
to APHIS.HPAI.BCAP.audits@usda.gov
or by postal mail to: Biosecurity Audit
Reconsideration, 920 Main Campus
Drive, Raleigh, NC 27606. The request
for reconsideration must be in writing,
state all the facts and reasons upon
which the producer relies to show that
the producer wrongfully failed the
biosecurity audit, and be received by the
Biosecurity Compliance Audit Program
Manager within 14 calendar days of
communication of the reviewer’s final
audit determination. After receipt of the
reconsideration request, the process
proceeds as follows:
(i) The Biosecurity Compliance Audit
Program Manager will review the
reconsideration request, the audit
package prepared by the auditor, and
the reviewer’s final audit determination.
If the Biosecurity Compliance Audit
Program Manager determines that the
producer wrongfully failed the
biosecurity audit, he or she will change
the final audit determination from fail to
pass. The auditor will notify the
producer of the change in writing, and
the Biosecurity Compliance Audit
Program Manager will close the
reconsideration request. If the
Biosecurity Compliance Audit Program
Manager agrees that the producer failed
the biosecurity audit, the
reconsideration process will continue to
a panel review.
(ii) A panel consisting of the State
Animal Health Official of the State
where the premises is located, the
APHIS Area Veterinarian in Charge, and
the Biosecurity Compliance Audit
Program Manager will review the
reconsideration request, the audit
package prepared by the auditor, and
the reviewer’s final audit determination.
The panel’s decision is final and will be
communicated to the producer as
promptly as circumstances allow and
will state, in writing, the reasons for the
decision.
(5) A final audit determination of pass
for a premises that had a biosecurity
audit conducted in accordance with
paragraph (f)(1)(i) or (ii) of this section
will be valid for six (6) months, unless
the premises changes its poultry
biosecurity plan, biosecurity
coordinator, ownership, or
infrastructure. If such premises makes
any of the aforementioned changes, the
premises must pass a new biosecurity
audit conducted in accordance with
paragraph (f)(1)(i) or (ii) of this section,
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15:56 Dec 30, 2024
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as applicable, prior to the movement of
poultry onto the premises.
(6) The biosecurity audit tool
referenced in paragraph (f)(1) of this
section will be reviewed by APHIS on
an annual basis and revised as follows:
(i) Standard process for revising the
biosecurity audit tool: If the
Administrator determines that revisions
to the biosecurity audit tool are
necessary, APHIS will publish a notice
in the Federal Register advising the
public of the Administrator’
determination. The notice will describe
the proposed revisions and the reasons
for the proposed revisions and will
invite public comment on the proposed
revisions.
(ii) Immediate process for revising the
biosecurity audit tool: If the
Administrator determines that the
biosecurity audit tool is no longer
sufficient for auditors to use to conduct
biosecurity audits pursuant to paragraph
(f)(1)(i) or (ii) of this section, APHIS will
immediately update the biosecurity
audit tool. APHIS will publish a notice
in the Federal Register advising the
public of the Administrator’s
determination. The notice will specify
the revisions and the reasons for the
revisions, provide an effective date for
the revisions, and will invite public
comment on the revisions.
*
*
*
*
*
Done in Washington, DC, this 23rd day of
December 2024.
Jennifer Moffitt,
Undersecretary, Marketing and Regulatory
Programs, USDA.
[FR Doc. 2024–31384 Filed 12–30–24; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 101
[Docket No. FDA–2000–N–0011]
Uniform Compliance Date for Food
Labeling Regulations
Food and Drug Administration,
Department of Health and Human
Services (HHS).
ACTION: Final action; announcement of a
uniform compliance date.
AGENCY:
The Food and Drug
Administration (FDA or we) is
establishing January 1, 2028, as the
uniform compliance date for food
labeling regulations that are published
on or after January 1, 2025, and on or
before December 31, 2026. We
SUMMARY:
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Sfmt 4700
periodically announce uniform
compliance dates for new food labeling
requirements to minimize the economic
impact of labeling changes.
DATES: This final action is effective
December 31, 2024. Either electronic or
written comments on the final action
must be submitted by March 3, 2025.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. The https://
www.regulations.gov electronic filing
system will accept comments until
11:59 p.m. Eastern Time at the end of
March 3, 2025. Comments received by
mail/hand delivery/courier (for written/
paper submissions) will be considered
timely if they are received 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.’’
E:\FR\FM\31DER1.SGM
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Federal Register / Vol. 89, No. 250 / Tuesday, December 31, 2024 / Rules and Regulations
Instructions: All submissions received
must include the Docket No. FDA–
2000–N–0011 for ‘‘Uniform Compliance
Date for Food Labeling Regulations.’’
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.’’ We
will review this copy, including the
claimed confidential information, in our
consideration of comments. The 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:
Lauren Kleinman, Human Foods
Program (HFS–24), Food and Drug
Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–2378.
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
15:56 Dec 30, 2024
Jkt 265001
I. Background
We periodically issue regulations
requiring changes in the labeling of
food. If the compliance dates of these
labeling changes were not coordinated,
the cumulative economic impact on the
food industry of having to respond
separately to each change would be
substantial. Therefore, we periodically
have announced uniform compliance
dates for new food labeling
requirements (see, e.g., the Federal
Register of October 19, 1984 (49 FR
41019); December 24, 1996 (61 FR
67710); December 27, 1996 (61 FR
68145); December 23, 1998 (63 FR
71015); November 20, 2000 (65 FR
69666); December 31, 2002 (67 FR
79851); December 21, 2006 (71 FR
76599); December 8, 2008 (73 FR
74349); December 15, 2010 (75 FR
78155); November 28, 2012 (77 FR
70885); December 10, 2014 (79 FR
73201); November 25, 2016 (81 FR
85156); December 20, 2018 (83 FR
65294); January 6, 2021 (86 FR 462); and
January 3, 2023 (88 FR 6)). Use of a
uniform compliance date provides for
an orderly and economical industry
adjustment to new labeling
requirements by allowing sufficient lead
time to plan for the use of existing label
inventories and the development of new
labeling materials.
II. Analysis of Environmental Impact
We have determined under 21 CFR
25.30(k) that this action is of a type that
does not individually or cumulatively
have a significant effect on the human
environment. Therefore, neither an
environmental assessment nor an
environmental impact statement is
required.
III. Paperwork Reduction Act of 1995
This final action contains no
collections of information. Therefore,
clearance by the Office of Management
and Budget under the Paperwork
Reduction Act of 1995 is not required.
IV. Conclusion
This action does not relate to existing
requirements for compliance dates
contained in final rules published
before January 1, 2025. Therefore, the
compliance dates for all final rules
published by FDA in the Federal
Register before January 1, 2025, will be
the date stated in the respective final
rule. We generally encourage industry to
comply with new labeling regulations as
quickly as feasible, however. Thus,
when industry members voluntarily
change their labels, it is appropriate that
they incorporate any new requirements
that have been published as final
regulations up to that time.
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106997
In rulemaking that began with
publication of a proposed rule on April
15, 1996 (61 FR 16422), and ended with
a final rule on December 24, 1996 (61
FR 67710) (together ‘‘the 1996
rulemaking’’), we provided notice and
an opportunity for comment on the
practice of establishing uniform
compliance dates by issuance of a final
rule announcing the date. We received
no comments objecting to this practice
during the 1996 rulemaking, nor have
we received comments objecting to this
practice since we last published a
uniform compliance date final rule on
January 3, 2023 (88 FR 6).
We find for good cause that notice
and public procedure thereon are
unnecessary because this action is
uncontroversial and is consistent with
FDA’s past practice over many years. In
this proceeding, FDA has identified a
uniform compliance date that is
approximately 3 years after the date of
publication of this final action,
consistent with past uniform
compliance date rules. Moreover,
interested parties will have an
opportunity to comment on the
compliance date for each individual
food labeling regulation as part of the
rulemaking process for that regulation.
Consequently, FDA finds that notice
and public procedure thereon are
unnecessary for this final action.
However, under 21 CFR 10.40(e)(1), we
are providing an opportunity for
comment on whether the uniform
compliance date established by this
final action should be modified or
revoked.
In addition, we find good cause for
this final action to become effective on
the date of publication of this action. A
delayed effective date is unnecessary in
this case because this action does not
impose any new regulatory
requirements on affected parties.
Instead, this final action provides
affected parties with notice of our intent
to identify January 1, 2028, as the
compliance date for final food labeling
regulations that require changes in the
labeling of food products and that
publish on or after January 1, 2025, and
on or before December 31, 2026, unless
special circumstances justify a different
compliance date. Thus, affected parties
do not need time to prepare before the
rule takes effect. Therefore, we find
good cause for this final action to
become effective on the date of
publication of this action.
The uniform compliance date is only
relevant to final FDA food labeling
regulations that require changes in the
labeling of food products and that
publish on or after January 1, 2025, and
on or before December 31, 2026. All
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Federal Register / Vol. 89, No. 250 / Tuesday, December 31, 2024 / Rules and Regulations
food products subject to the January 1,
2028, compliance date must comply
with the appropriate regulations when
initially introduced into interstate
commerce on or after January 1, 2028.
If any food labeling regulation involves
special circumstances that justify a
compliance date other than January 1,
2028, we will determine for that
regulation an appropriate compliance
date, which will be specified when the
final regulation is published.
Dated: December 26, 2024.
P. Ritu Nalubola,
Associate Commissioner for Policy.
[FR Doc. 2024–31419 Filed 12–30–24; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HOUSING AND
URBAN DEVELOPMENT
24 CFR Parts 5, 92, 93, 570, 574, 576,
and 578
[Docket No. FR–6057–N–06]
Housing Opportunity Through
Modernization Act: Implementation of
Sections 102, 103, and 104; Extension
of Compliance Date and Safe Harbor
Implementation
Office of the Assistant
Secretary for Community Planning and
Development, U.S. Department of
Housing and Urban Development
(HUD).
ACTION: Final rule; extension of
compliance date.
AGENCY:
This document extends the
compliance date for HUD’s final rule
entitled ‘‘Housing Opportunity Through
Modernization Act of 2016:
Implementation of Sections 102, 103,
and 104’’ (HOTMA final rule) for
Community Planning and Development
(CPD) programs. Specifically, HUD is
extending the compliance date for the
HOME Investment Partnerships program
(HOME), HOME-American Rescue Plan
program, Housing Trust Fund (HTF),
Housing Opportunities for Persons With
AIDS (HOPWA), Community
Development Block Grant program
(CDBG), Emergency Solution Grants
(ESG), Continuum of Care (CoC)
programs, and CPD programs funded
through competitive processes
(Competitive Programs). HUD is
extending the compliance deadline for
all grantees and allowing grantees that
are ready to comply to set an earlier
compliance date between January 1,
2024, and January 1, 2026. In addition,
HUD is permitting the implementation
of certain income safe harbors
established in the HOTMA final rule
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SUMMARY:
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15:56 Dec 30, 2024
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prior to the extended HOTMA
compliance date. HUD is taking this
action due to delays in updating the
HUD systems to comply with HOTMA
and to allow additional time for
jurisdictions, participants, and grantees
to incorporate HUD’s income and asset
requirements into their own programs
and flexibility to transition
implementing HOTMA requirements
under their own timelines.
DATES: The compliance date for the final
rule published February 14, 2023, at 88
FR 9600, is extended. CPD participating
jurisdictions, participants, and grantees
(CPD grantees) subject to 24 CFR parts
5, 92, 93, 570, 574, 576, and 578, or who
apply the income requirements in 24
CFR part 5 pursuant to Notices of
Funding Opportunity (NOFOs), are not
required to comply with the changes
established by the HOTMA final rule
until January 1, 2026.
FOR FURTHER INFORMATION CONTACT: For
HOME and the HTF, Milagro Fisher,
Senior Affordable Housing Specialist,
Office of Affordable Housing Programs,
at telephone (202) 708–2684, Room
7160; for HOPWA, Lisa Steinhauer,
Senior Program Specialist, Office of
HIV/AIDS Housing, at telephone (215)
861–7651, Room 7248; for CDBG, B.
Cory Schwartz, Deputy Director, State &
Small Cities Division, at telephone (202)
402–4105, Room 7282. The mailing
address for each office contact is
Department of Housing and Urban
Development, 451 Seventh Street SW,
Washington, DC 20410–7000. HUD
welcomes and is prepared to receive
calls from individuals who are deaf or
hard of hearing, as well as individuals
with speech or communication
disabilities. To learn more about how to
make an accessible telephone call,
please visit: https://www.fcc.gov/
consumers/guides/telecommunicationsrelay-service-trs.
SUPPLEMENTARY INFORMATION:
I. Background
On February 14, 2023, HUD published
the HOTMA final rule (88 FR 9600). The
HOTMA final rule established a January
1, 2024, effective date for the revisions
it made to HUD’s income regulations at
24 CFR parts 5, 92, 93, 570, and 574.
These revisions also affected CPD
programs subject to 24 CFR parts 576
and 578, as well as Competitive
Programs using NOFOs that reference
the regulations at 24 CFR part 5. On
September 29, 2023, HUD’s Office of
Public and Indian Housing (PIH) and
Office of Housing (Housing) issued joint
notification PIH 2023–27/H 2023–10,
which enabled Public Housing Agencies
(PHAs) and multifamily owners to
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establish their own compliance dates for
sections 102 and 104 of HOTMA as
early as January 1, 2024, and no later
than January 1, 2025. Similarly, on
December 8, 2023, HUD published the
Housing Opportunity Through
Modernization Act: Implementation of
Sections 102, 103, and 104; Extension of
Compliance Date (88 FR 85648) to
extend the compliance date of the
HOTMA final rule to January 1, 2025,
for all CPD programs that use HUD’s 24
CFR part 5 income regulations.
II. Further Extensions of the HOTMA
Final Rule Compliance Date
On September 18, 2024, PIH
announced that PHAs were not to
implement and comply with the section
102 and 104 income and assets
provisions in the HOTMA final rule by
January 1, 2025. This extension was due
to delays in updating the HUD systems
to comply with the rule. Then, on
September 20, 2024, Housing issued
notification H 2024–09 to announce that
multifamily owners were not to
implement and comply with the
HOTMA final rule until July 1, 2025.
This was also due to delays in updating
the HUD systems to comply with the
rule. Now, HUD has determined that
CPD grantees receiving assistance
through CPD programs, which often
overlap with PIH and multifamily
programs, must be provided with
certain flexibilities. HUD is
communicating these flexibilities
through this document.
HUD’s determination that these
flexibilities are necessary was made in
light of the fact that CPD grantees may
not be able to comply with the
requirements of the HOTMA final rule
until after HUD has provided the
guidance and performed the software
updates necessary for CPD grantees to
implement the HOTMA final rule. Even
after the necessary guidance is provided
and updates to HUD systems are made,
CPD grantees will still need additional
time to incorporate this guidance into
their program policies and procedures
and to update their own systems and
software. Therefore, in recognition of
these operational issues and challenges,
HUD is allowing CPD grantees to set
their own compliance dates for the
applicable HOTMA final rule
provisions. These compliance dates may
be as early as January 1, 2024, and no
later than January 1, 2026. Until these
new compliance dates, CPD grantees
must continue to adhere, as applicable,
to the requirements found in both their
program regulations and the regulations
at 24 CFR 5.603, 24 CFR 5.609, 24 CFR
5.611, and 24 CFR 5.617 as they existed
prior to January 1, 2024. Furthermore,
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Agencies
[Federal Register Volume 89, Number 250 (Tuesday, December 31, 2024)]
[Rules and Regulations]
[Pages 106996-106998]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-31419]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 101
[Docket No. FDA-2000-N-0011]
Uniform Compliance Date for Food Labeling Regulations
AGENCY: Food and Drug Administration, Department of Health and Human
Services (HHS).
ACTION: Final action; announcement of a uniform compliance date.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is establishing
January 1, 2028, as the uniform compliance date for food labeling
regulations that are published on or after January 1, 2025, and on or
before December 31, 2026. We periodically announce uniform compliance
dates for new food labeling requirements to minimize the economic
impact of labeling changes.
DATES: This final action is effective December 31, 2024. Either
electronic or written comments on the final action must be submitted by
March 3, 2025.
ADDRESSES: You may submit comments as follows. Please note that late,
untimely filed comments will not be considered. The https://www.regulations.gov electronic filing system will accept comments until
11:59 p.m. Eastern Time at the end of March 3, 2025. Comments received
by mail/hand delivery/courier (for written/paper submissions) will be
considered timely if they are received 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.''
[[Page 106997]]
Instructions: All submissions received must include the Docket No.
FDA-2000-N-0011 for ``Uniform Compliance Date for Food Labeling
Regulations.'' 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.'' We will review
this copy, including the claimed confidential information, in our
consideration of comments. The 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: Lauren Kleinman, Human Foods Program
(HFS-24), Food and Drug Administration, 5001 Campus Dr., College Park,
MD 20740, 240-402-2378.
SUPPLEMENTARY INFORMATION:
I. Background
We periodically issue regulations requiring changes in the labeling
of food. If the compliance dates of these labeling changes were not
coordinated, the cumulative economic impact on the food industry of
having to respond separately to each change would be substantial.
Therefore, we periodically have announced uniform compliance dates for
new food labeling requirements (see, e.g., the Federal Register of
October 19, 1984 (49 FR 41019); December 24, 1996 (61 FR 67710);
December 27, 1996 (61 FR 68145); December 23, 1998 (63 FR 71015);
November 20, 2000 (65 FR 69666); December 31, 2002 (67 FR 79851);
December 21, 2006 (71 FR 76599); December 8, 2008 (73 FR 74349);
December 15, 2010 (75 FR 78155); November 28, 2012 (77 FR 70885);
December 10, 2014 (79 FR 73201); November 25, 2016 (81 FR 85156);
December 20, 2018 (83 FR 65294); January 6, 2021 (86 FR 462); and
January 3, 2023 (88 FR 6)). Use of a uniform compliance date provides
for an orderly and economical industry adjustment to new labeling
requirements by allowing sufficient lead time to plan for the use of
existing label inventories and the development of new labeling
materials.
II. Analysis of Environmental Impact
We have determined under 21 CFR 25.30(k) that this action is of a
type that does not individually or cumulatively have a significant
effect on the human environment. Therefore, neither an environmental
assessment nor an environmental impact statement is required.
III. Paperwork Reduction Act of 1995
This final action contains no collections of information.
Therefore, clearance by the Office of Management and Budget under the
Paperwork Reduction Act of 1995 is not required.
IV. Conclusion
This action does not relate to existing requirements for compliance
dates contained in final rules published before January 1, 2025.
Therefore, the compliance dates for all final rules published by FDA in
the Federal Register before January 1, 2025, will be the date stated in
the respective final rule. We generally encourage industry to comply
with new labeling regulations as quickly as feasible, however. Thus,
when industry members voluntarily change their labels, it is
appropriate that they incorporate any new requirements that have been
published as final regulations up to that time.
In rulemaking that began with publication of a proposed rule on
April 15, 1996 (61 FR 16422), and ended with a final rule on December
24, 1996 (61 FR 67710) (together ``the 1996 rulemaking''), we provided
notice and an opportunity for comment on the practice of establishing
uniform compliance dates by issuance of a final rule announcing the
date. We received no comments objecting to this practice during the
1996 rulemaking, nor have we received comments objecting to this
practice since we last published a uniform compliance date final rule
on January 3, 2023 (88 FR 6).
We find for good cause that notice and public procedure thereon are
unnecessary because this action is uncontroversial and is consistent
with FDA's past practice over many years. In this proceeding, FDA has
identified a uniform compliance date that is approximately 3 years
after the date of publication of this final action, consistent with
past uniform compliance date rules. Moreover, interested parties will
have an opportunity to comment on the compliance date for each
individual food labeling regulation as part of the rulemaking process
for that regulation. Consequently, FDA finds that notice and public
procedure thereon are unnecessary for this final action. However, under
21 CFR 10.40(e)(1), we are providing an opportunity for comment on
whether the uniform compliance date established by this final action
should be modified or revoked.
In addition, we find good cause for this final action to become
effective on the date of publication of this action. A delayed
effective date is unnecessary in this case because this action does not
impose any new regulatory requirements on affected parties. Instead,
this final action provides affected parties with notice of our intent
to identify January 1, 2028, as the compliance date for final food
labeling regulations that require changes in the labeling of food
products and that publish on or after January 1, 2025, and on or before
December 31, 2026, unless special circumstances justify a different
compliance date. Thus, affected parties do not need time to prepare
before the rule takes effect. Therefore, we find good cause for this
final action to become effective on the date of publication of this
action.
The uniform compliance date is only relevant to final FDA food
labeling regulations that require changes in the labeling of food
products and that publish on or after January 1, 2025, and on or before
December 31, 2026. All
[[Page 106998]]
food products subject to the January 1, 2028, compliance date must
comply with the appropriate regulations when initially introduced into
interstate commerce on or after January 1, 2028. If any food labeling
regulation involves special circumstances that justify a compliance
date other than January 1, 2028, we will determine for that regulation
an appropriate compliance date, which will be specified when the final
regulation is published.
Dated: December 26, 2024.
P. Ritu Nalubola,
Associate Commissioner for Policy.
[FR Doc. 2024-31419 Filed 12-30-24; 8:45 am]
BILLING CODE 4164-01-P