[Federal Register Volume 84, Number 190 (Tuesday, October 1, 2019)]
[Proposed Rules]
[Page 52055]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-20958]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 573

[Docket No. FDA-2019-F-3911]


Evonik Corp.; Filing of Food Additive Petition (Animal Use)

AGENCY: Food and Drug Administration, HHS.

ACTION: Notification; petition for rulemaking.

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SUMMARY: The Food and Drug Administration (FDA or we) is announcing 
that Evonik Corp. has filed a petition proposing that the food additive 
regulations be amended to provide for the safe use of silicon dioxide 
as an anticaking agent, grinding aid, antifoaming agent, or carrier in 
animal feed components (ingredients, intermediate premixes, premixes, 
supplements, or concentrates).

DATES: The food additive petition was filed on July 24, 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.

FOR FURTHER INFORMATION CONTACT: Chelsea Cerrito, Center for Veterinary 
Medicine, Food and Drug Administration, 7519 Standish Pl., Rockville, 
MD 20855, 240-402-6729, [email protected].

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 2308) has been filed by Evonik Corp., 1707 
Barrett Lakes Blvd. NW, Suite 340, Kennesaw, GA 30144. 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 silicon 
dioxide as an anticaking agent, grinding aid, antifoaming agent, or 
carrier in animal feed components (ingredients, intermediate premixes, 
premixes, supplements, or concentrates).
    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.

    Dated: September 23, 2019.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2019-20958 Filed 9-30-19; 8:45 am]
 BILLING CODE 4164-01-P