[Federal Register Volume 61, Number 166 (Monday, August 26, 1996)]
[Notices]
[Page 43772]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-21727]



[[Page 43772]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 96F-0291]


ICI Americas 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 ICI 
Americas Inc., has filed a petition proposing that the food additive 
regulations be amended to provide for the safe use of 12-hydroxystearic 
acid-polyethylene glycol (minimum MW 200) block copolymer as an 
surfactant in the manufacture of paper and paperboard intended for use 
in contact with food.
DATES: Written comments on the petitioner's environmental assessment by 
September 25, 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 6B4519) has been filed by ICI Americas Inc., 
3411 Silverside Rd., Wilmington, DE 19850. The petition proposes to 
amend the food additive regulations to provide for the safe use of 12-
hydroxystearic acid-polyethylene glycol (minimum MW 200) block 
copolymer as a surfactant in the manufacture of paper and paperboard 
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 
September 25, 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).

    Dated: August 8, 1996.
Alan M. Rulis,
Director, Office of Premarket Approval, Center for Food Safety and 
Applied Nutrition.
[FR Doc. 96-21727 Filed 8-23-96; 8:45 am]
BILLING CODE 4160-01-F