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Kemin Industries Food Additive Petition for Animal Use

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Published March 4th, 2026
Detected March 5th, 2026
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Summary

The Food and Drug Administration (FDA) is seeking public comment on a food additive petition filed by Kemin Industries, Inc. for animal use. The comment period for this proposed rule closes on April 3, 2026.

What changed

The Food and Drug Administration (FDA) has published a notice regarding a food additive petition submitted by Kemin Industries, Inc. for animal use. This filing initiates a public comment period, allowing interested parties to provide input on the proposed additive. The specific details of the petition, including the nature of the additive and its intended use in animals, are subject to review during this consultation phase.

Regulated entities, particularly those in the food and animal feed industries, should review the petition and consider submitting comments by the deadline of April 3, 2026. Failure to comment may result in the FDA proceeding with the petition without considering potential concerns or objections. This action represents an opportunity to influence the regulatory approval process for new food additives intended for animal consumption.

What to do next

  1. Review the Kemin Industries food additive petition for animal use.
  2. Submit comments to the FDA by April 3, 2026, if applicable.

Source document (simplified)

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Proposed Rule

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

A Proposed Rule by the Food and Drug Administration on 03/04/2026

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  2. Document Details Published Content - Document Details Agencies Department of Health and Human Services Food and Drug Administration Agency/Docket Number Docket No. FDA-2026-F-2048 CFR 21 CFR 573 Document Citation 91 FR 10525 Document Number 2026-04284 Document Type Proposed Rule Pages 10525-10526 (2 pages) Publication Date 03/04/2026 Published Content - Document Details
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  • Document Details Published Content - Document Details Agencies Department of Health and Human Services Food and Drug Administration Agency/Docket Number Docket No. FDA-2026-F-2048 CFR 21 CFR 573 Document Citation 91 FR 10525 Document Number 2026-04284 Document Type Proposed Rule Pages 10525-10526 (2 pages) Publication Date 03/04/2026 Published Content - Document Details
  • Document Dates Published Content - Document Dates Comments Close 04/03/2026 Effective Date 2026-02-07 Dates Text The food additive petition was filed on February 7, 2026. Either electronic or written comments on the petitioner's environmental assessment must be submitted by April 3, 2026. Published Content - Document Dates
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Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use)

Comment Due Date 04/03/2026 Docket ID FDA-2026-F-2048 Supporting Documents Environmental Assessment (Phase I) Chromium Propionate in Layer and Breeding Chicken Diets Enhanced Content - Regulations.gov Data

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Published Document: 2026-04284 (91 FR 10525) This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.

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Department of Health and Human Services
Food and Drug Administration
  1. 21 CFR Part 573
  2. [Docket No. FDA-2026-F-2048]

AGENCY:

Food and Drug Administration, HHS.

ACTION:

Notification of petition.

SUMMARY:

The Food and Drug Administration (FDA or we) is announcing that we have filed a food additive petition, submitted by Kemin Industries, Inc., proposing that we amend our food additive regulations to provide for the safe use of chromium propionate as a source of chromium in food for layer and breeding chickens.

DATES:

The food additive petition was filed on February 7, 2026. Either electronic or written comments on the petitioner's environmental assessment must be submitted by April 3, 2026.

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 April 3, 2026. 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-2026-F-2048 for “Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use).” 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.” FDA will review this copy, including the claimed confidential information, in its 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.

( printed page 10526)

FOR FURTHER INFORMATION CONTACT:

Lauren LaPlace, Center for Veterinary Medicine, Food and Drug Administration, 5001 Campus Dr., College Park, MD 20740, 301-348-1819, Lauren.LaPlace@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

Under section 409(b)(5) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 348(b)(5)), we are giving notice that we have filed a food additive petition (FAP 2325), submitted by Kemin Industries, Inc, 1900 Scott Avenue, Des Moines, IA 50317. The petition proposes to amend in 21 CFR part 573 —Food Additives Permitted in Feed and Drinking Water of Animals, to provide for the safe use of chromium propionate to be used as a source of chromium in food for layer and breeding chickens.

We are reviewing the potential environmental impact of this petition. To encourage public participation consistent with regulations issued under the National Environmental Policy Act (40 CFR 1501.4(b)), we are placing the environmental assessment submitted with the petition that is the subject of this notice on public display at the Dockets Management Staff (see DATES and ADDRESSES) for public review and comment.

We will also place on public display, at the Dockets Management Staff and at https://www.regulations.gov, any amendments to, or comments on, the petitioner's environmental assessment without further announcement in the Federal Register. If, based on our review, we find that an environmental impact statement is not required, and this petition results in a regulation, we will publish the notice of availability of our finding of no significant impact and the evidence supporting that finding with the regulation in the Federal Register in accordance with 21 CFR 25.51(b).

Grace R. Graham,

Deputy Commissioner for Policy, Legislation, and International Affairs.

[FR Doc. 2026-04284 Filed 3-3-26; 8:45 am]

BILLING CODE 4164-01-P

Published Document: 2026-04284 (91 FR 10525)

Classification

Agency
Office of the Federal Register
Published
March 4th, 2026
Compliance deadline
April 3rd, 2026 (20 days)
Instrument
Consultation
Legal weight
Non-binding
Stage
Draft
Change scope
Substantive

Who this affects

Applies to
Food manufacturers Drug manufacturers Pharmaceutical companies
Geographic scope
National (US)

Taxonomy

Primary area
Food Safety
Operational domain
Compliance
Topics
Animal Feed Regulatory Submissions

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