[Federal Register Volume 61, Number 98 (Monday, May 20, 1996)]
[Notices]
[Page 25228]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-12568]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 96F-0145]
Albright & Wilson, 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
Albright & Wilson, Ltd., has filed a petition proposing that the food
additive regulations be amended to provide for the safe use of
tetrakis(hydroxymethyl)phosphonium sulfate as a slimicide for use in
the manufacture of paper and paperboard intended to contact food.
DATES: Written comments on the petitioner's environmental assessment by
June 19, 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: Daniel N. Harrison, Center for Food
Safety and Applied Nutrition (HFS-216), Food and Drug Administration,
200 C St. SW., Washington, DC 20204-0002, 202-418-3080.
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 5B4472) has been filed by Albright & Wilson,
Ltd., c/o Delta Analytical Corp., 7910 Woodmont Ave., suite 1000,
Bethesda, MD 20814. The petition proposes to amend the food additive
regulations in Sec. 176.300 Slimicides (21 CFR 176.300) to provide for
the safe use of tetrakis(hydroxymethyl)phosphonium sulfate as a
slimicide in the manufacture of paper and paperboard intended to
contact 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 June
19, 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: April 30, 1996.
Alan M. Rulis,
Director, Office of Premarket Approval, Center for Food Safety and
Applied Nutrition.
[FR Doc. 96-12568 File6d 5-17-96; 8:45 am]
BILLING CODE 4160-01-F
