Alcide Corp.; Filing of Food Additive Petition
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[Federal Register: May 23, 2001 (Volume 66, Number 100)]
[Notices]
[Page 28525-28526]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr23my01-98]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 01F-0233]
Alcide Corp.; 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
Alcide Corp. has filed a petition proposing that the food additive
regulations be amended to provide for the safe use of acidified sodium
chlorite solutions as an antimicrobial agent in processing waters
applied to processed fruits and vegetables.
DATES: Submit written comments on the petitioner's environmental
assessment by June 22, 2001.
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 1A4729) has been filed by Alcide Corp., 8561
154th Ave. NE., Redmond, WA 98052. The petition proposes to amend the
food additive regulations in Sec. 173.325 Acidified sodium chlorite
solutions (21 CFR 173.325) to provide for the safe use of acidified
sodium chlorite solutions as an antimicrobial agent in processing
waters applied to processed fruits and vegetables.
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 June 22, 2001. 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
[[Page 28526]]
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 4, 2001.
Alan M. Rulis,
Director, Office of Premarket Approval, Center for Food Safety and
Applied Nutrition.
[FR Doc. 01-13068 Filed 5-22-01; 8:45 am]
BILLING CODE 4160-01-S
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