[Federal Register Volume 75, Number 137 (Monday, July 19, 2010)]
[Rules and Regulations]
[Pages 41725-41726]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-17565]
[[Page 41725]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 573
[Docket No. FDA-2008-F-0151] (formerly Docket No. 2007F-0478)
Food Additives Permitted in Feed and Drinking Water of Animals;
Ammonium Formate
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
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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 ammonium formate 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 July 19, 2010. Submit either electronic
or written objections and requests for a hearing by August 18, 2010.
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-2008-F-0151, 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 number for this rulemaking. All objections received will be
posted without change to http://www.regulations.gov, including any
personal information provided. For detailed 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:
[email protected].
SUPPLEMENTARY INFORMATION:
I. Background
In a notice published in the Federal Register of January 11, 2008
(73 FR 2055), FDA announced that a food additive petition (animal use)
(FAP 2258) had been filed by Kemira Oyj, Porkkalantatu 3, PO Box 330,
001000 Helsinki, Finland. The petition proposed to amend the food
additive regulations to provide for the safe use of partially
ammoniated formic acid as an acidifying agent at levels not to exceed
1.2 percent in swine feed. Subsequently, it was determined that the
food additive is more accurately described as ammonium formate. The
notice of filing provided for a 60-day comment period on the
petitioner's environmental assessment. No comments have been received.
II. Conclusion
FDA concludes that the data establish the safety and utility of
ammonium formate for use as proposed with modification and that the
food additive regulations should be amended as set forth in this
document.
III. 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 any materials
that are not available for public disclosure before making the
documents available for inspection.
IV. 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.
V. Objections
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. Each objection shall be separately
numbered, and each numbered objection shall specify with particularity
the provisions 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.
0
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
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1. The authority citation for 21 CFR part 573 continues to read as
follows:
Authority: 21 U.S.C. 321, 342, 348.
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2. Add Sec. 573.170 to read as follows:
Sec. 573.170 Ammonium formate.
The food additive, partially ammonium formate, may be safely used
in the manufacture of complete swine feeds in accordance with the
following prescribed conditions:
(a) The additive is manufactured by the reaction of 99.5 percent
ammonia gas and 99 percent formic acid in a continuous loop reactor to
produce a solution made up of 37 percent ammonium salt of formic acid
and 62 percent formic acid.
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(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.
(c) To assure safe use of the additive, in addition to the other
information required by the Federal Food, Drug, and Cosmetic Act (the
act), the label and labeling shall contain:
(1) The name of the additive.
(2) Adequate directions for use including a statement that ammonium
formate must be uniformly applied and thoroughly mixed into complete
swine feeds and that the complete swine feeds so treated shall be
labeled as containing ammonium formate.
(d) To assure safe use of the additive, in addition to the other
information required by the act and paragraph (c) of this section, the
label and labeling shall contain:
(1) Appropriate warnings and safety precautions concerning ammonium
formate (37 percent ammonium salt of formic acid and 62 percent formic
acid).
(2) Statements identifying ammonium formate in formic acid (37
percent ammonium salt of formic acid and 62 percent formic acid) as a
corrosive and possible severe irritant.
(3) Information about emergency aid in case of accidental exposure
as follows:
(i) 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.
(ii) Contact address and telephone number for reporting adverse
reactions or to request a copy of the Material Safety Data Sheet
(MSDS).
Dated: July 14, 2010.
Tracey H. Forfa,
Acting Director, Center for Veterinary Medicine.
[FR Doc. 2010-17565 Filed 7-16-10; 8:45 am]
BILLING CODE 4160-01-S