[Federal Register Volume 61, Number 92 (Friday, May 10, 1996)]
[Notices]
[Pages 21473-21474]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-11789]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 96F-0136]
Johnson Matthey Chemicals; Filing of Food Additive Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that
Johnson Matthey Chemicals has filed a petition proposing that the food
additive regulations be amended to provide for the safe use of silver
chloride-coated titanium dioxide as a preservative in polymeric
coatings for polyolefin films intended for use in contact with food.
DATES: Written comments on petitioner's environmental assessment by
June 10, 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 6B4503) has been filed on behalf of Johnson
Matthey Chemicals, c/o Technical Assessment Systems, Inc., The Flour
Mill, 1000 Potomac St. NW., Washington, DC 20007. The petition proposes
to amend the food additive regulations in Sec. 175.320 Resinous and
polymeric coatings for polyolefin films (21 CFR 175.320) to provide for
the safe use of silver chloride-coated titanium dioxide as a
preservative in polymeric coatings for polyolefin films 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
display at the Dockets Management Branch (address above) for public
review and comment. Interested persons may, on or before June 10, 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).
[[Page 21474]]
Dated: April 23, 1996.
Eugene C. Coleman,
Acting Director, Office of Premarket Approval, Center for Food Safety
and Applied Nutrition.
[FR Doc. 96-11789 Filed 5-9-96; 8:45 am]
BILLING CODE 4160-01-F
