[Federal Register Volume 60, Number 137 (Tuesday, July 18, 1995)]
[Notices]
[Page 36811]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-17639]



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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 95F-0174]


H.B. Fuller Co.; 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 H.B. 
Fuller Co. has filed a petition proposing that the food additive 
regulations be amended to provide for the safe use of nonanoic acid, 
lactic acid, citric acid, sodium 1-octane sulfonate, tertiary 
butylhydroquinone, and the sodium salt of tetrapropylene-1,1-oxybis-
benzenesulfonic acid as components of a sanitizing solution intended 
for general use on food-contact surfaces.

DATES: Written comments on the petitioner's environmental assessment by 
August 17, 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 5B4462) has been filed by H.B. Fuller Co., c/o 
SRS International Corp., 1625 K St. NW., suite 1000, Washington, DC 
20006-1604. The petition proposes to amend the food additive 
regulations in Sec. 178.1010 Sanitizing solutions (21 CFR 178.1010) to 
provide for the safe use of nonanoic acid, lactic acid, citric acid, 
sodium 1-octane sulfonate, tertiary butylhydroquinone, and the sodium 
salt of tetrapropylene-1,1-oxybis-benzenesulfonic acid as components of 
a sanitizing solution intended for general use on food-contact 
surfaces.
    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 August 
17, 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: July 5, 1995.
Alan M. Rulis,
Acting Director, Office of Premarket Approval, Center for Food Safety 
and Applied Nutrition.
[FR Doc. 95-17639 Filed 7-17-95; 8:45 am]
BILLING CODE 4160-01-F