Food Additives Permitted in Feed and Drinking Water of Animals:
Federal Register: February 9, 2011 (Volume 76, Number 27)
Rules and Regulations
Page 7106-7107
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
DOCID:fr09fe11-6
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration 21 CFR Part 573
Docket No. FDA-2009-F-0525
Food Additives Permitted in Feed and Drinking Water of Animals;
Formic Acid
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
SUMMARY: The Food and Drug Administration (FDA) is amending the regulations for food additives permitted in feed and drinking water of animals to provide for the safe use of formic acid as an acidifying agent in swine feed. This action is in response to a food additive petition filed by Kemira Oyj of Finland.
DATES: This rule is effective February 9, 2011. Submit either electronic or written objections and requests for a hearing by March 11, 2011. See section V of this document for information on the filing of objections.
ADDRESSES: You may submit either electronic or written objections and a request for a hearing, identified by Docket No. FDA-2009-F-0525, by any of the following methods:
Electronic Submissions
Submit electronic objections in the following ways:
Federal eRulemaking Portal: http://www.regulations.gov. Follow the instructions for submitting comments.
Written Submissions
Submit written objections in the following ways:
Fax: 301-827-6870.
Mail/Hand delivery/Courier (For paper, disk, or CD-ROM submissions): Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Instructions: All submissions received must include the Agency name and Docket No. FDA-2009-F-0525 for this rulemaking. All objections received will be posted without change to http://www.regulations.gov, including any personal information provided. For additional information on submitting objections, see the ``Objections'' heading of the
SUPPLEMENTARY INFORMATION section of this document.
Docket: For access to the docket to read background documents or objections received, go to http://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 Division of
Dockets Management, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Isabel W. Pocurull, Center for
Veterinary Medicine (HFV-226), Food and Drug Administration, 7519
Standish Pl., Rockville, MD 20855, 240-453-6853, e-mail: isabel.pocurull@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
-
Background
In a notice published in the Federal Register of December 7, 2009
(74 FR 64091), FDA announced that a food additive petition (animal use)
(FAP 2262) had been filed by Kemira Oyj, Porkkalantatu 3, P.O. Box 330, 001000 Helsinki, Finland. The petition proposed to amend the food additive regulations to provide for the safe use of formic acid as an acidifying agent at levels not to exceed 1.2 percent in swine feed. The notice of filing provided for a 30-day comment period on the petitioner's environmental assessment. One comment was received that was not substantive.
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Conclusion
FDA concludes that the data establish the safety and utility of formic acid for use as proposed with modification and that the food additive regulations should be amended as set forth in this document.
-
Public Disclosure
In accordance with Sec. 571.1(h) (21 CFR 571.1(h)), the petition and the documents that FDA considered and relied upon in reaching its decision to approve the petition are available for inspection at the
Center for Veterinary Medicine by appointment with the information contact person (see FOR FURTHER INFORMATION CONTACT). As provided in
Sec. 571.1(h), the Agency will delete from the documents materials that are not available for public disclosure before making the documents available for inspection.
-
Environmental Impact
The Agency has determined under 21 CFR 25.32(r) that this action is of a type that does not individually or cumulatively have a significant effect on the human environment. Therefore, neither an environmental assessment nor an environmental impact statement is required.
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Objections and Hearing Requests
Any person who will be adversely affected by this regulation may file with the Division of Dockets Management (see ADDRESSES) either electronic or written objections (see DATES). Each objection shall be separately numbered, and each numbered objection shall specify with particularity the provision of the regulation to which objection is made and the grounds for the objection. Each numbered objection on which a hearing is requested shall specifically so state. Failure to request a hearing for any particular objection shall constitute a waiver of the right to a hearing on that objection. Each numbered objection for which a hearing is requested shall include a detailed description and analysis of the specific factual information intended to be presented in support of the objection in the event that a hearing is held. Failure to include such a description and analysis for any particular objection shall constitute a waiver of the right to a hearing on the objection. It is only necessary to send one set of documents. It is no longer necessary to send three copies of all documents. Identify documents with the docket number found in brackets in the heading of this document. Any objections received in response to the regulation may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.
List of Subjects in 21 CFR Part 573
Animal feeds, Food additives.
Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs and redelegated to the Center for Veterinary Medicine, 21 CFR part 573 is amended as follows:
PART 573--FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF
ANIMALS 0 1. The authority citation for 21 CFR part 573 continues to read as follows:
Authority: 21 U.S.C. 321, 342, 348. 0 2. Revise Sec. 573.480 to read as follows:
Sec. 573.480 Formic acid.
The food additive, formic acid, may be safely used in accordance with the following conditions:
(a) The additive is used as a preservative in hay crop silage in an amount not to exceed 2.25 percent of
Page 7107
the silage on a dry weight basis or 0.45 percent when direct cut, as follows:
(1) The top foot of silage stored should not contain formic acid and
(2) Silage should not be fed to livestock within 4 weeks of treatment.
(b) The additive is used or intended for use as a feed acidifying agent, to lower the pH, in complete swine feeds at levels not to exceed 1.2 percent of the complete feed.
(1) The additive consists of not less than 85 percent formic acid
(CAS 64-18-6).
(2) The additive meets the following specifications:
(i) Free methyl alcohol not to exceed 1,000 parts per million
(ppm);
(ii) Methyl formate not to exceed 1,000 ppm; and
(iii) Moisture not to exceed 15 percent.
(3) To assure safe use of the additive, in addition to the other information required by the Federal Food, Drug and Cosmetic Act, the label and labeling shall contain:
(i) The name of the additive.
(ii) Adequate directions for use including a statement that formic acid must be uniformly applied and thoroughly mixed into complete swine feeds and that the complete swine feeds so treated shall be labeled as containing formic acid.
(4) To assure safe use of the additive, in addition to the other information required by the Federal Food, Drug, and Cosmetic Act and paragraph (b)(3) of this section, the label and labeling shall contain:
(i) Appropriate warnings and safety precautions concerning formic acid (85 percent formic acid).
(ii) Statements identifying formic acid (85 percent formic acid) as a corrosive and possible severe irritant.
(iii) Information about emergency aid in case of accidental exposure.
(A) Statements reflecting requirements of applicable sections of the Superfund Amendments and Reauthorization Act (SARA), and the
Occupational Safety and Health Administration's (OSHA) human safety guidance regulations.
(B) Contact address and telephone number for reporting adverse reactions or to request a copy of the Material Safety Data Sheet
(MSDS).
Dated: February 3, 2011.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
FR Doc. 2011-2789 Filed 2-8-11; 8:45 am
BILLING CODE 4160-01-P
