Food Labeling: Front-of-Package Nutrition Information; Extension of Comment Period, 19664-19665 [2025-08204]
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19664
Federal Register / Vol. 90, No. 89 / Friday, May 9, 2025 / Proposed Rules
aircraft in air commerce by prescribing
regulations for practices, methods, and
procedures the Administrator finds
necessary for safety in air commerce.
This regulation is within the scope of
that authority because it addresses an
unsafe condition that is likely to exist or
develop on products identified in this
rulemaking action.
Regulatory Findings
The FAA determined that this
proposed AD would not have federalism
implications under Executive Order
13132. This proposed AD would not
have a substantial direct effect on the
States, on the relationship between the
national government and the States, or
on the distribution of power and
responsibilities among the various
levels of government.
For the reasons discussed above, I
certify this proposed regulation:
(1) Is not a ‘‘significant regulatory
action’’ under Executive Order 12866,
(2) Would not affect intrastate
aviation in Alaska, and
(3) Would not have a significant
economic impact, positive or negative,
on a substantial number of small entities
under the criteria of the Regulatory
Flexibility Act.
List of Subjects in 14 CFR Part 39
Air transportation, Aircraft, Aviation
safety, Incorporation by reference,
Safety.
The Proposed Amendment
Accordingly, under the authority
delegated to me by the Administrator,
the FAA proposes to amend 14 CFR part
39 as follows:
PART 39—AIRWORTHINESS
DIRECTIVES
1. The authority citation for part 39
continues to read as follows:
■
Authority: 49 U.S.C. 106(g), 40113, 44701.
§ 39.13
2. The FAA amends § 39.13 by adding
the following new airworthiness
directive:
■
lotter on DSK11XQN23PROD with PROPOSALS1
Airbus Helicopters Deutschland GmbH
(AHD): Docket No. FAA–2025–0750;
Project Identifier MCAI–2022–01325–R.
(a) Comments Due Date
The FAA must receive comments on this
airworthiness directive (AD) by June 23,
2025.
(b) Affected ADs
None.
(c) Applicability
This AD applies to Airbus Helicopters
Deutschland GmbH (AHD) Model MBB–BK
117 D–3 helicopters, certificated in any
16:07 May 08, 2025
(d) Subject
Joint Aircraft Service Component (JASC)
Code: 2432, Battery/Charger System.
(e) Unsafe Condition
This AD was prompted by reports of
momentary direct current (DC) power
interruption in flight of both essential busses.
The FAA is issuing this AD to address DC
power interruption through updated
procedures. The unsafe condition, if not
addressed, could result in loss of control of
the helicopter or reduced situational
awareness.
(f) Compliance
Comply with this AD within the
compliance times specified, unless already
done.
(g) Requirements
Except as specified in paragraph (h) of this
AD: Comply with all required actions and
compliance times specified in, and in
accordance with, EASA AD 2022–0208. The
owner/operator (pilot) holding at least a
private pilot certificate may revise the
existing RFM for your helicopter and must
enter compliance with this paragraph of the
AD into the helicopter maintenance records
in accordance with 14 CFR 43.9(a) and
91.417(a)(2)(v). The record must be
maintained as required by 14 CFR 91.417,
121.380, or 135.439.
(h) Exceptions to EASA AD 2022–0208
(1) Where paragraph (1) of EASA AD 2022–
0208 specifies to inform all flight crews and
operate the helicopter accordingly, this AD
does not require those actions.
(2) Where paragraph (2) of EASA AD 2022–
0208 specifies ‘‘the RFM emergency and
malfunction procedure, is an acceptable
method’’ this AD requires replacing that text
with ‘‘the RFM emergency and malfunction
procedure, as defined in this AD, is an
acceptable method.’’
(3) This AD does not adopt the ‘‘Remarks’’
section of EASA AD 2022–0208.
(i) Special Flight Permit
Special flight permits are prohibited.
[Amended]
VerDate Sep<11>2014
category, as identified in European Union
Aviation Safety Agency AD 2022–0208, dated
October 11, 2022 (EASA AD 2022–0208).
Jkt 265001
(j) Alternative Methods of Compliance
(AMOCs)
(1) The Manager, International Validation
Branch, FAA, has the authority to approve
AMOCs for this AD, if requested using the
procedures found in 14 CFR 39.19. In
accordance with 14 CFR 39.19, send your
request to your principal inspector or local
Flight Standards District Office, as
appropriate. If sending information directly
to the manager of the International Validation
Branch, send it to the attention of the person
identified in paragraph (k) of this AD and
email to: AMOC@faa.gov.
(2) Before using any approved AMOC,
notify your appropriate principal inspector,
or lacking a principal inspector, the manager
of the local flight standards district office/
certificate holding district office.
PO 00000
Frm 00005
Fmt 4702
Sfmt 4702
(k) Related Information
For more information about this AD,
contact Dan McCully, Aviation Safety
Engineer, FAA, 1600 Stewart Avenue, Suite
410, Westbury, NY 11590; phone: (303) 342–
1080; email: william.mccully@faa.gov.
(l) Material Incorporated by Reference
(1) The Director of the Federal Register
approved the incorporation by reference of
the material listed in this paragraph under 5
U.S.C. 552(a) and 1 CFR part 51.
(2) You must use this material as
applicable to do the actions required by this
AD, unless this AD specifies otherwise.
(i) European Union Aviation Safety Agency
(EASA) AD 2022–0208, dated October 11,
2022.
(ii) [Reserved]
(3) For EASA material identified in this
AD, contact EASA, Konrad-Adenauer-Ufer 3,
50668 Cologne, Germany; phone: +49 221
8999 000; email: ADs@easa.europa.eu;
website: easa.europa.eu. You may find the
EASA material on the EASA website at
ad.easa.europa.eu.
(4) You may view this material at the FAA,
Office of the Regional Counsel, Southwest
Region, 10101 Hillwood Parkway, Room 6N–
321, Fort Worth, TX 76177. For information
on the availability of this material at the
FAA, call (817) 222–5110.
(5) You may view this material at the
National Archives and Records
Administration (NARA). For information on
the availability of this material at NARA,
visit www.archives.gov/federal-register/cfr/
ibr-locations or email fr.inspection@nara.gov.
Issued on May 5, 2025.
Steven W. Thompson,
Acting Deputy Director, Compliance &
Airworthiness Division, Aircraft Certification
Service.
[FR Doc. 2025–08075 Filed 5–8–25; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 101
[Docket No. FDA–2024–N–2910]
RIN 0910–AI80
Food Labeling: Front-of-Package
Nutrition Information; Extension of
Comment Period
AGENCY:
Food and Drug Administration,
HHS.
Proposed rule; extension of
comment period.
ACTION:
The Food and Drug
Administration (FDA or we) is
extending the comment period for the
proposed rule entitled ‘‘Food Labeling:
Front-of-Package Nutrition Information’’
that appeared in the Federal Register of
SUMMARY:
E:\FR\FM\09MYP1.SGM
09MYP1
Federal Register / Vol. 90, No. 89 / Friday, May 9, 2025 / Proposed Rules
January 16, 2025. We are taking this
action in response to requests for an
extension to allow interested parties
additional time to submit comments.
DATES: FDA is extending the comment
period on the proposed rule published
January 16, 2025 (90 FR 5426), by 60
days. Either electronic or written
comments must be submitted by July 15,
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
July 15, 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’’).
lotter on DSK11XQN23PROD with PROPOSALS1
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
VerDate Sep<11>2014
16:07 May 08, 2025
Jkt 265001
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2024–N–2910 for ‘‘Food Labeling: Frontof-Package Nutrition Information.’’
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:
Claudine Kavanaugh, Office of Nutrition
and Food Labeling, Human Foods
Program, Food and Drug
Administration, 5001 Campus Dr.,
College Park, MD 20740, 301–796–4647;
PO 00000
Frm 00006
Fmt 4702
Sfmt 4702
19665
or Deirdre Jurand or Alexandra
Beliveau, Office of Policy, Regulations,
and Information, Human Foods
Program, Food and Drug
Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–2378.
SUPPLEMENTARY INFORMATION: In the
Federal Register of January 16, 2025,
FDA published a proposed rule entitled
‘‘Food Labeling: Front-of-Package
Nutrition Information’’ (90 FR 5426)
with a 120-day period for submission of
public comments. We have received
requests to extend the comment period.
The requests expressed concern that the
current 120-day comment period does
not allow sufficient time to develop a
meaningful response to the proposed
rule.
We have considered the requests and
are extending the comment period for
the proposed rule for 60 days, until July
15, 2025. We believe that a 60-day
extension allows adequate time for
interested parties to submit comments
without significantly delaying
rulemaking on the important issues in
the proposed rule.
Dated: May 5, 2025.
Grace R. Graham,
Deputy Commissioner for Policy, Legislation,
and International Affairs.
[FR Doc. 2025–08204 Filed 5–8–25; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
33 CFR Part 165
[Docket Number USCG–2025–0210]
RIN 1625–AA87
Security Zone; Upper Mississippi
River, Saint Louis, MO
Coast Guard, DHS.
Notice of proposed rulemaking.
AGENCY:
ACTION:
The Coast Guard proposes
establishing a permanent security zone
for certain waters of the Upper
Mississippi River adjacent to the
Jefferson Barracks military installation,
Saint Louis, MO. This proposed
rulemaking would prohibit persons and
vessels from operating or anchoring
within the Security zone unless
authorized by the Captain of the Port
Sector Upper Mississippi River or a
designated representative. This action is
necessary to ensure no unauthorized
entry into the waters adjacent to the
military installation to safeguard the
installation from sabotage or other
SUMMARY:
E:\FR\FM\09MYP1.SGM
09MYP1
Agencies
[Federal Register Volume 90, Number 89 (Friday, May 9, 2025)]
[Proposed Rules]
[Pages 19664-19665]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-08204]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 101
[Docket No. FDA-2024-N-2910]
RIN 0910-AI80
Food Labeling: Front-of-Package Nutrition Information; Extension
of Comment Period
AGENCY: Food and Drug Administration, HHS.
ACTION: Proposed rule; extension of comment period.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is extending the
comment period for the proposed rule entitled ``Food Labeling: Front-
of-Package Nutrition Information'' that appeared in the Federal
Register of
[[Page 19665]]
January 16, 2025. We are taking this action in response to requests for
an extension to allow interested parties additional time to submit
comments.
DATES: FDA is extending the comment period on the proposed rule
published January 16, 2025 (90 FR 5426), by 60 days. Either electronic
or written comments must be submitted by July 15, 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 July 15, 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.''
Instructions: All submissions received must include the Docket No.
FDA-2024-N-2910 for ``Food Labeling: Front-of-Package Nutrition
Information.'' 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: Claudine Kavanaugh, Office of
Nutrition and Food Labeling, Human Foods Program, Food and Drug
Administration, 5001 Campus Dr., College Park, MD 20740, 301-796-4647;
or Deirdre Jurand or Alexandra Beliveau, Office of Policy, Regulations,
and Information, Human Foods Program, Food and Drug Administration,
5001 Campus Dr., College Park, MD 20740, 240-402-2378.
SUPPLEMENTARY INFORMATION: In the Federal Register of January 16, 2025,
FDA published a proposed rule entitled ``Food Labeling: Front-of-
Package Nutrition Information'' (90 FR 5426) with a 120-day period for
submission of public comments. We have received requests to extend the
comment period. The requests expressed concern that the current 120-day
comment period does not allow sufficient time to develop a meaningful
response to the proposed rule.
We have considered the requests and are extending the comment
period for the proposed rule for 60 days, until July 15, 2025. We
believe that a 60-day extension allows adequate time for interested
parties to submit comments without significantly delaying rulemaking on
the important issues in the proposed rule.
Dated: May 5, 2025.
Grace R. Graham,
Deputy Commissioner for Policy, Legislation, and International Affairs.
[FR Doc. 2025-08204 Filed 5-8-25; 8:45 am]
BILLING CODE 4164-01-P