[Federal Register Volume 65, Number 114 (Tuesday, June 13, 2000)]
[Notices]
[Page 37155]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 00-14906]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 00F-1332]
Ecolab, Inc.; Filing of Food Additive Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing that
Ecolab, Inc., has filed a petition proposing that the food additive
regulations be amended to provide for the safe use of a mixture of
peroxyacetic acid, octanoic acid, acetic acid, hydrogen peroxide,
peroxyoctanoic acid, and 1-hydroxyethylidene-1,1-diphosphonic acid as
an antimicrobial agent on red meat carcasses.
DATES: Submit written comments on the petitioner's environmental
assessment by July 13, 2000.
ADDRESSES: Submit written comments to the Dockets Management Branch
(HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Robert L. Martin, Center for Food
Safety and Applied Nutrition (HFS-215), Food and Drug Administration,
200 C St. SW., Washington, DC 20204-0001, 202-418-3074.
SUPPLEMENTARY INFORMATION: Under the Federal Food, Drug, and Cosmetic
Act (sec. 409(b)(5) (21 U.S.C. 348(b)(5))), notice is given that a food
additive petition (FAP 0A4720) has been filed by Ecolab, Inc., Ecolab
Center, 370 Wabasha St., St. Paul, MN 55102. The petition proposes to
amend the food additive regulations in 21 CFR part 173 (21 CFR part
173) to provide for the safe use of a mixture of peroxyacetic acid,
octanoic acid, acetic acid, hydrogen peroxide, peroxyoctanoic acid, and
1-hydroxyethylidene-1,1-diphosphonic acid as an antimicrobial agent on
red meat carcasses.
The potential environmental impact of this action is being
reviewed. To encourage public participation consistent with regulations
issued under the National Environmental Policy Act (40 CFR 1501.4(b)),
the agency is placing the environmental assessment submitted with the
petition that is the subject of this notice on public display at the
Dockets Management Branch (address above) for public review and
comment. Interested persons may submit to the Dockets Management Branch
written comments by July 13, 2000. Two copies of any comments are to be
submitted, except that individuals may submit one copy. Comments are to
be identified with the docket number found in brackets in the heading
of this document. Received comments may be seen in the Dockets
Management Branch between 9 a.m. and 4 p.m., Monday through Friday. FDA
will also place on public display any amendments to, or comments on,
the petitioner's environmental assessment without further announcement
in the Federal Register. If, based on its review, the agency finds that
an environmental impact statement is not required and this petition
results in a regulation, the notice of availability of the agency's
finding of no significant impact and the evidence supporting that
finding will be published with the regulation in the Federal Register
in accordance with 21 CFR 25.40(c).
Dated: May 30, 2000.
Alan M. Rulis,
Director, Office of Premarket Approval, Center for Food Safety and
Applied Nutrition.
[FR Doc. 00-14906 Filed 6-12-00; 8:45 am]
BILLING CODE 4160-01-F