Notice2023-28512

Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use); Chromium Propionate; Correction

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
December 27, 2023

Issuing agencies

Health and Human Services DepartmentFood and Drug Administration

Abstract

The Food and Drug Administration is correcting a notice entitled "Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use)" that appeared in the Federal Register of July 27, 2023. The document announced that we filed a petition, submitted by Kemin Industries, Inc., proposing that the food additive regulations be amended to provide for the safe use of chromium propionate to be used as a source of chromium in turkey feed. The document was published with an incorrect docket number. This document corrects that error.

Full Text

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<title>Federal Register, Volume 88 Issue 247 (Wednesday, December 27, 2023)</title>
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[Federal Register Volume 88, Number 247 (Wednesday, December 27, 2023)]
[Notices]
[Page 89460]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2023-28512]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2023-F-5500]


Kemin Industries, Inc.; Filing of Food Additive Petition (Animal 
Use); Chromium Propionate; Correction

AGENCY: Food and Drug Administration, HHS

ACTION: Notification of petition; correction.

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SUMMARY: The Food and Drug Administration is correcting a notice 
entitled ``Kemin Industries, Inc.; Filing of Food Additive Petition 
(Animal Use)'' that appeared in the Federal Register of July 27, 2023. 
The document announced that we filed a petition, submitted by Kemin 
Industries, Inc., proposing that the food additive regulations be 
amended to provide for the safe use of chromium propionate to be used 
as a source of chromium in turkey feed. The document was published with 
an incorrect docket number. This document corrects that error.

FOR FURTHER INFORMATION CONTACT: Wasima Wahid, Center for Veterinary 
Medicine (HFV-221), Food and Drug Administration, 12225 Wilkins Ave., 
Rockville, MD 20852, 240-402-5857, <a href="/cdn-cgi/l/email-protection#3a4d5b4953575b144d5b52535e7a5c5e5b14525249145d554c"><span class="__cf_email__" data-cfemail="91e6f0e2f8fcf0bfe6f0f9f8f5d1f7f5f0bff9f9e2bff6fee7">[email&#160;protected]</span></a>.

SUPPLEMENTARY INFORMATION: In the Federal Register of Thursday, July 
27, 2023 (88 FR 48406) in FR Doc. 2023-15913, the following correction 
is made:
    On page 48406, in the first column, in the header of the document, 
``Docket No. FDA-2023-F-2415'' is corrected to read ``Docket No. FDA-
2023-F-5500''.

    Dated: December 21, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023-28512 Filed 12-26-23; 8:45 am]
BILLING CODE 4164-01-P


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Indexed from Federal Register on December 27, 2023.

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