[Federal Register Volume 62, Number 83 (Wednesday, April 30, 1997)]
[Notices]
[Pages 23467-23468]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-11078]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 97C-0171]
Toyo-Morton, 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
Toyo-Morton, Ltd., has filed a petition proposing that the food
additive regulations be amended to provide for the safe use of
polyester-epoxy-urethane adhesive for use as a nonfood contact layer of
laminated articles intended for use in contact with food.
DATES: Written comments on the petitioner's environmental assessment by
May 30, 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: Daniel N. Harrison, Center for Food
[[Page 23468]]
Safety and Applied Nutrition (HFS-215), Food and Drug Administration,
200 C St. SW., Washington, DC 20204, 202-418-3084.
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 7B4538) has been filed by Toyo-Morton, Ltd., c/o
Keller and Heckman LLP, 1001 G St. NW., suite 500 West, Washington, DC
20001. The petition proposes to amend the food additive regulations in
Sec. 177.1390 Laminate structures for use at temperatures of 250 deg. F
and above (21 CFR 177.1390) to provide for the safe use of polyester-
epoxy-urethane adhesive for use as a nonfood contact layer of laminated
articles 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 May 30,
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: April 17, 1997.
Alan M. Rulis,
Director, Office of Premarket Approval, Center for Food Safety and
Applied Nutrition.
[FR Doc. 97-11078 Filed 4-29-97; 8:45 am]
BILLING CODE 4160-01-F