[Federal Register Volume 59, Number 160 (Friday, August 19, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-20450]
[[Page Unknown]]
[Federal Register: August 19, 1994]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 94F-0257]
Betz Laboratories; Filing of Food Additive Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that Betz
Laboratories has filed a petition proposing that the food additive
regulations be amended to provide for the safe use of the copolymer of
the sodium salt of acrylic acid with polyethyleneglycol allyl ether in
paper mill boilers.
DATES: Written comments on the petitioner's environmental assessment by
September 19, 1994.
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 4B4426) has been filed by Betz Laboratories,
4636 Somerton Rd., Trevose, PA 19053. The petition proposes that the
food additive regulations in Sec. 176.170 Components of paper and
paperboard in contact with aqueous and fatty foods (21 CFR 176.170) be
amended to provide for the safe use of the copolymer of the sodium salt
of acrylic acid with polyethyleneglycol allyl ether in paper mill
boilers.
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 (insert date 30 days
after date of publication in the Federal Register), 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 11, 1994.
Fred R. Shank,
Director, Center for Food Safety and Applied Nutrition.
[FR Doc. 94-20450 Filed 8-18-94; 8:45 am]
BILLING CODE 4160-01-F
