[Federal Register Volume 61, Number 139 (Thursday, July 18, 1996)]
[Notices]
[Page 37484]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-18284]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 96F-0213]
Toyobo Co., Ltd.; 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
Toyobo Co., Ltd., has filed a petition proposing that the food additive
regulations be amended to provide for the safe use of 1,4-
benzenedicarboxylic acid, polymer with 1,4-butanediol, ()-2-
butanedioic acid, 1,2-ethanediol, ethyl-2-propenoate, hexanedioic acid
and 2-propenoic acid, graft, in nylon 6 and nylon 6 modified with nylon
MXD-6 articles intended for use in contact with food.
DATES: Written comments on petitioner's environmental assessment by
August 19, 1996.
ADDRESSES: Submit written comments to the Dockets Management Branch
(HFA-305), Food and Drug Administration, 12420 Parklawn Dr., rm. 1-23,
Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: Vir D. Anand, Center for Food Safety
and Applied Nutrition (HFS-216), Food and Drug Administration, 200 C
St. SW., Washington, DC 20204, 202-418-3081.
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 6B4511) has been filed by Toyobo Co., Ltd., 2-1-
1 Hon Katata Otsu, Shiga 520-02, Japan. The petition proposes to amend
the food additive regulations to provide for the safe use of 1,4-
benzenedicarboxylic acid, polymer with 1,4-butanediol, ()-2-
butanedioic acid, 1,2-ethanediol, ethyl 2-propenoate, hexanedioic acid
and 2-propenoic acid, graft, in nylon 6 and nylon 6 modified with nylon
MXD-6 articles intended for use in contact with food. The graft resins
of this type are generically called copolyester-graft-copolymer.
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
display at the Dockets Management Branch (address above) for public
review and comment. Interested persons may, on or before August 19,
1996, 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: June 20, 1996.
George H. Pauli,
Acting Director, Office of Premarket Approval, Center for Food Safety
and Applied Nutrition.
[FR Doc. 96-18284 Filed 7-17-96; 8:45 am]
BILLING CODE 4160-01-F
