[Federal Register Volume 59, Number 158 (Wednesday, August 17, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-20131]
[[Page Unknown]]
[Federal Register: August 17, 1994]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 94F-0246]
Kuraray Co.; 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
Kuraray Co. has filed a petition proposing that the food additive
regulations be amended to provide for the safe use of ethylene-vinyl
acetate-vinyl alcohol copolymers with broadened specifications that
include a decreased minimum acceptable ethylene content and an
increased maximum permitted level of migration of ethylene-vinyl
acetate-vinyl alcohol oligomers.
DATES: Written comments on petitioner's environmental assessment by
September 16, 1994
ADDRESSES: Submit written comments to the Dockets Management Branch
(HFA-305), Food and Drug Administration, rm. 1-23, 12420 Parklawn Dr.,
Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: Diane E. Robertson, Center for Food
Safety and Applied Nutrition (HFS-216), Food and Drug Administration,
200 C St. SW., Washington, DC 20204, 202-254-9511.
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 4B4421) has been filed by Kuraray Co., 1001 G
St., NW., suite 500 West, Washington, DC 20001. The petition proposes
to amend Sec. 177.1360 Ethylene-vinyl acetate-vinyl alcohol copolymers
(21 CFR 177.1360) of the food additive regulations to provide for the
safe use of ethylene-vinyl acetate-vinyl alcohol copolymers with
broadened specifications that include a decreased minimum acceptable
ethylene content and an increased maximum permitted level of migration
of ethylene-vinyl acetate-vinyl alcohol oligomers.
The potential environmental impact of this action is being
reviewed. To encourage public participation consistent with regulations
promulgated 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, on or before September 16, 1994,
submit to the Dockets Management Branch (address above) written
comments. 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 office above 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: August 5, 1994.
Fred R. Shank,
Director, Center for Food Safety and Applied Nutrition.
[FR Doc. 94-20131 Filed 8-16-94; 8:45 am]
BILLING CODE 4160-01-F
