[Federal Register Volume 60, Number 29 (Monday, February 13, 1995)]
[Notices]
[Pages 8243-8244]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-3556]



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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 95F-0017]


Robinson Brothers 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 
Robinson Brothers Ltd., has filed a petition proposing that the food 
additive regulations be amended to provide for the safe use of 
diisopropyl xanthogen polysulfide as a component of rubber articles 
intended for repeated use in contact with food.

DATES: Written comments on the petitioner's environmental assessment by 
March 15, 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: Diane E. Robertson, Center for Food 
Safety and Applied Nutrition (HFS-216), Food and Drug Administration, 
200 C St. SW., Washington, DC 20204, 202-418-3089.

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 5B4437) has been filed by Robinson Brothers 
Ltd., Phoenix St., West Bromwich, West Midland, B70 OAH, England. The 
petition proposes to amend the food additive regulations in 
[[Page 8244]] Sec. 177.2600 Rubber articles intended for repeated use 
(21 CFR 177.2600) to provide for the safe use of diisopropyl xanthogen 
polysulfide as a component of rubber articles intended for repeated 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 March 
15, 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 the evidence supporting that 
finding will be published with the regulation in the Federal Register 
in accordance with 21 CFR 25.40(c).

    Dated: February 3, 1995.
Alan M. Rulis,
Acting Director, Office of Premarket Approval, Center for Food Safety 
and Applied Nutrition.
[FR Doc. 95-3556 Filed 2-10-95; 8:45 am]
BILLING CODE 4160-01-F