[Federal Register Volume 60, Number 120 (Thursday, June 22, 1995)]
[Notices]
[Page 32526]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-15348]



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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration
[Docket No. 95F-0122]


Hempel Coatings (USA), Inc.; 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 
Hempel Coatings (USA), Inc., has filed a petition proposing that the 
food additive regulations be amended to provide for the safe use of 
meta-xylylenediamine and 3-diethylaminopropylamine as components of 
articles intended for food-contact use.

DATES: Written comments on the petitioner's environmental assessment by 
July 24, 1995.

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: Julius Smith, Center for Food Safety 
and Applied Nutrition (HFS-216), Food and Drug Administration, 200 C 
St. SW., Washington, DC 20204, 202-254-9500.

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 5B4457) has been filed by Hempel Coatings (USA), 
Inc., 6901 Cavalcade St., Houston, TX 77028. The petition proposes to 
amend the food additive regulations in Sec. 175.300 Resinous and 
polymeric coatings (21 CFR 175.300) to provide for the safe use of 
meta-xylylenediamine and 3-diethylaminopropylamine as components of 
articles intended for food-contact use.
    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 July 
24, 1995, 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 evidence supporting that finding 
will be published with the regulation in the Federal Register in 
accordance with 21 CFR 25.40(c).

    Dated: June 13, 1995.
Alan M. Rulis,
 Acting Director, Office of Premarket Approval, Center for Food Safety 
and Applied Nutrition.
[FR Doc. 95-15348 Filed 6-21-95; 8:45 am]
BILLING CODE 4160-01-F