[Federal Register Volume 62, Number 11 (Thursday, January 16, 1997)]
[Notices]
[Page 2373]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-1116]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 97F-0004]
Ciba Specialty Chemicals 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 Ciba
Specialty Chemicals Corp. has filed a petition proposing that the food
additive regulations be amended to provide for the safe use of 2-(4,6-
diphenyl-1,3,5-triazin-2-yl)-5-(hexyloxy)phenol as a light stabilizer/
ultraviolet (UV) absorber for polycarbonate resins and polyester
elastomers intended for use in contact with food.
DATES: Written comments on the petitioner's environmental assessment by
February 18, 1997.
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 7B4531) has been filed by Ciba Specialty
Chemicals Corp., 540 White Plains Rd., Tarrytown, NY 10591-9005. The
petition proposes to amend the food additive regulations in
Sec. 178.2010 Antioxidants and/or stabilizers for polymers (21 CFR
178.2010) to provide for the safe use of 2-(4,6-diphenyl-1,3,5-triazin-
2-yl)-5-(hexyloxy)phenol as a light stabilizer/UV absorber for
polycarbonate resins complying with 21 CFR 177.1580 and polyester
elastomers complying with 21 CFR 177.1590 intended for use in contact
with food.
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
February 18, 1997, 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: December 26, 1996.
Alan M. Rulis,
Director, Office of Premarket Approval, Center for Food Safety and
Applied Nutrition.
[FR Doc. 97-1116 Filed 1-15-97; 8:45 am]
BILLING CODE 4160-01-F
