2020-02664. LANXESS Corporation; Filing of Food Additive Petition (Animal Use)  

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    AGENCY:

    Food and Drug Administration, HHS.

    ACTION:

    Notification; petition for rulemaking.

    SUMMARY:

    The Food and Drug Administration (FDA or we) is announcing that LANXESS Corporation has filed a petition proposing that the food additive regulations be amended to provide for the safe use of calcium formate as a feed acidifying agent, to lower the pH, in complete feeds for swine or poultry.

    DATES:

    The food additive petition was filed on December 27, 2019.

    ADDRESSES:

    For access to the docket, 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.

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    FOR FURTHER INFORMATION CONTACT:

    Carissa Adams, Center for Veterinary Start Printed Page 7683Medicine, Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-402-6283, Carissa.Adams@fda.hhs.gov.

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    SUPPLEMENTARY INFORMATION:

    Under the Federal Food, Drug, and Cosmetic Act (section 409(b)(5) (21 U.S.C. 348(b)(5))), notice is given that a food additive petition (FAP 2310) has been filed by LANXESS Corporation, 111 RIDC Park West Dr., Pittsburgh, PA 15275. The petition proposes to amend Title 21 of the Code of Federal Regulations (CFR) in part 573 (21 CFR part 573) Food Additives Permitted in Feed and Drinking Water of Animals to provide for the safe use of calcium formate as a feed acidifying agent, to lower the pH, in complete feeds for swine or poultry.

    The petitioner has claimed that this action is categorically excluded under 21 CFR 25.32(r) because it is of a type that does not individually or cumulatively have a significant effect on the human environment. In addition, the petitioner has stated that, to their knowledge, no extraordinary circumstances exist. If FDA determines a categorical exclusion applies, neither an environmental assessment nor an environmental impact statement is required. If FDA determines a categorical exclusion does not apply, we will request an environmental assessment and make it available for public inspection.

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    Dated: February 5, 2020.

    Lowell J. Schiller,

    Principal Associate Commissioner for Policy.

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    [FR Doc. 2020-02664 Filed 2-10-20; 8:45 am]

    BILLING CODE 4164-01-P

Document Information

Published:
02/11/2020
Department:
Food and Drug Administration
Entry Type:
Proposed Rule
Action:
Notification; petition for rulemaking.
Document Number:
2020-02664
Dates:
The food additive petition was filed on December 27, 2019.
Pages:
7682-7683 (2 pages)
Docket Numbers:
Docket No. FDA-2020-F-0151
PDF File:
2020-02664.pdf
CFR: (1)
21 CFR 573