Food Labeling, Infant Formula Requirements, Food Additives and Generally Recognized as Safe Substances, New Dietary Ingredient Notification; Technical Amendments; Correction, 33550 [2023-10602]
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33550
Federal Register / Vol. 88, No. 100 / Wednesday, May 24, 2023 / Rules and Regulations
List of Subjects in 14 CFR Part 25
Aircraft, Aviation safety, Reporting
and recordkeeping requirements.
Authority Citation
The authority citation for these
special conditions is as follows:
Authority: 49 U.S.C. 106(f), 106(g), 40113,
44701, 44702, and 44704.
The Special Conditions
Accordingly, pursuant to the
authority delegated to me by the
Administrator, the following special
conditions are issued as part of the type
certification basis for MHI RJ Aviation
ULC Model CL–600–2B19 airplanes, as
modified by B/E Aerospace Ltd.
The distribution system for the
passenger therapeutic oxygen system
must be designed and installed to meet
requirements as follows:
When oxygen is supplied to
passengers for both supplemental and
therapeutic purposes, the distribution
system must be designed for either—
(1) A source of supplemental oxygen
for protection following a loss of cabin
pressure, and a separate source for
therapeutic purposes; or
(2) A common source of supply with
means to separately reserve the
minimum supply required by the
passengers for supplemental use
following a loss of cabin pressure.
Issued in Kansas City, Missouri, on May
18, 2023.
Patrick R. Mullen,
Manager, Technical Policy Branch, Policy and
Standards Division, Aircraft Certification
Service.
[FR Doc. 2023–10987 Filed 5–23–23; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Mark Kantor, Office of Nutrition and
Food Labeling (HFS–830), Center for
Food Safety and Applied Nutrition,
Food and Drug Administration, 5001
Campus Dr., College Park, MD 20740,
240–402–1450; or Alexandra Jurewitz,
Office of Regulations and Policy (HFS–
024), Center for Food Safety and
Applied Nutrition, Food and Drug
Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–2378.
In the
Federal Register of Friday, March 24,
2023 (88 FR 17710 at 17718), an
incorrect abbreviation to ‘‘Potassium’’
appeared in § 101.9(j)(13)(ii)(B) of the
codified language. This document
corrects that error.
SUPPLEMENTARY INFORMATION:
List of Subjects in 21 CFR Part 101
Food Labeling, Nutrition, Reporting
and recordkeeping requirements.
1. The authority citation for part 101
continues to read as follows:
[Docket No. FDA–2022–N–2898]
Food Labeling, Infant Formula
Requirements, Food Additives and
Generally Recognized as Safe
Substances, New Dietary Ingredient
Notification; Technical Amendments;
Correction
ddrumheller on DSK120RN23PROD with RULES1
FOR FURTHER INFORMATION CONTACT:
■
21 CFR Part 101
Food and Drug Administration,
HHS.
Final rule; technical
amendments; correction.
ACTION:
The Food and Drug
Administration is correcting a final rule
entitled ‘‘Food Labeling, Infant Formula
SUMMARY:
16:25 May 23, 2023
Effective May 24, 2023.
PART 101—FOOD LABELING
Food and Drug Administration
VerDate Sep<11>2014
DATES:
For the reasons stated in the
preamble, FDA is correcting 21 CFR part
101 with the following correcting
amendment:
BILLING CODE 4910–13–P
AGENCY:
Requirements, Food Additives and
Generally Recognized as Safe
Substances, New Dietary Ingredient
Notification; Technical Amendments’’
that appeared in the Federal Register of
March 24, 2023. The final rule corrected
typographical errors, corrected errors in
sample labels, restored inadvertent
omissions, and updated office and
organization names, addresses, and
other references. The document was
published with an incorrect
abbreviation to ‘‘Potassium’’ in the
codified language. This document
corrects that error.
Jkt 259001
Authority: 15 U.S.C. 1453, 1454, 1455; 21
U.S.C. 321, 331, 342, 343, 348, 371; 42 U.S.C.
243, 264, 271.
§ 101.9
[Amended]
2. In § 101.9, amend paragraph
(j)(13)(ii)(B) by removing ‘‘Potassium—
Pot.’’ and replacing it with
‘‘Potassium—Potas.’’.
■
Dated: May 15, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023–10602 Filed 5–23–23; 8:45 am]
BILLING CODE 4164–01–P
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FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Part 27
[GN Docket No. 18–122; GN Docket No. 23–
97; DA 23–408; FR ID 141458]
Wireless Telecommunications Bureau
Announces C-Band Phase II
Certification Procedures
Federal Communications
Commission.
ACTION: Final action.
AGENCY:
In this document, the Federal
Communications Commission
(Commission) announces the
procedures related to the filing of Phase
II Certifications of Accelerated
Relocation (Certifications) and
implements the Commission’s
incremental reduction plan for Phase II
Accelerated Relocation Payments
(ARPs) as part of the ongoing transition
of the 3.7 GHz band.
DATES: Effective June 1, 2023.
ADDRESSES: Federal Communications
Commission, 45 L St. NE, Washington,
DC 20554.
FOR FURTHER INFORMATION CONTACT: For
additional information on this
proceeding, contact Susan Mort of the
Wireless Telecommunications Bureau,
at (202) 418–2429 or Susan.Mort@
fcc.gov.
SUMMARY:
This is a
summary of the document, Wireless
Telecommunications Bureau
Announces Procedures for Filing of CBand Phase II Certifications of
Accelerated Relocation and
Implementation of the Commission’s
Incremental Reduction Plan for Phase II
Accelerated Relocation Payments,
released on May 15, 2023. The full text
of this document is available for public
inspection online at https://
docs.fcc.gov/public/attachments/DA-23408A1.pdf.
1. With this document, the Bureau
adopts filing procedures for the
submission of Phase II Certifications, as
proposed in C-Band Phase II
Certification of Accelerated Relocation
Procedures and Implementation of the
Commission’s Incremental Reduction
Plan for Phase II Accelerated Relocation
Public Notice (Phase II Certification
Procedures and Incremental Reduction
Comment PN), released in March 2023
in this proceeding (88 FR 16932, Mar.
21, 2023). These procedures are
modeled after those previously adopted
for Phase I to allow eligible space
station operators to submit
Certifications, and stakeholders to file
related challenges, with respect to the
SUPPLEMENTARY INFORMATION:
E:\FR\FM\24MYR1.SGM
24MYR1
Agencies
[Federal Register Volume 88, Number 100 (Wednesday, May 24, 2023)]
[Rules and Regulations]
[Page 33550]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-10602]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 101
[Docket No. FDA-2022-N-2898]
Food Labeling, Infant Formula Requirements, Food Additives and
Generally Recognized as Safe Substances, New Dietary Ingredient
Notification; Technical Amendments; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; technical amendments; correction.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration is correcting a final rule
entitled ``Food Labeling, Infant Formula Requirements, Food Additives
and Generally Recognized as Safe Substances, New Dietary Ingredient
Notification; Technical Amendments'' that appeared in the Federal
Register of March 24, 2023. The final rule corrected typographical
errors, corrected errors in sample labels, restored inadvertent
omissions, and updated office and organization names, addresses, and
other references. The document was published with an incorrect
abbreviation to ``Potassium'' in the codified language. This document
corrects that error.
DATES: Effective May 24, 2023.
FOR FURTHER INFORMATION CONTACT: Mark Kantor, Office of Nutrition and
Food Labeling (HFS-830), Center for Food Safety and Applied Nutrition,
Food and Drug Administration, 5001 Campus Dr., College Park, MD 20740,
240-402-1450; or Alexandra Jurewitz, Office of Regulations and Policy
(HFS-024), Center for Food Safety and Applied Nutrition, Food and Drug
Administration, 5001 Campus Dr., College Park, MD 20740, 240-402-2378.
SUPPLEMENTARY INFORMATION: In the Federal Register of Friday, March 24,
2023 (88 FR 17710 at 17718), an incorrect abbreviation to ``Potassium''
appeared in Sec. 101.9(j)(13)(ii)(B) of the codified language. This
document corrects that error.
List of Subjects in 21 CFR Part 101
Food Labeling, Nutrition, Reporting and recordkeeping requirements.
For the reasons stated in the preamble, FDA is correcting 21 CFR
part 101 with the following correcting amendment:
PART 101--FOOD LABELING
0
1. The authority citation for part 101 continues to read as follows:
Authority: 15 U.S.C. 1453, 1454, 1455; 21 U.S.C. 321, 331, 342,
343, 348, 371; 42 U.S.C. 243, 264, 271.
Sec. 101.9 [Amended]
0
2. In Sec. 101.9, amend paragraph (j)(13)(ii)(B) by removing
``Potassium--Pot.'' and replacing it with ``Potassium--Potas.''.
Dated: May 15, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023-10602 Filed 5-23-23; 8:45 am]
BILLING CODE 4164-01-P