[Federal Register Volume 59, Number 101 (Thursday, May 26, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-12855]
[[Page Unknown]]
[Federal Register: May 26, 1994]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 94F-0153]
Kuraray International Corp.; Filing of Food Additive Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that
Kuraray International Corp. has filed a petition proposing that the
food additive regulations be amended to provide for the safe use of n-
octanol produced by a new manufacturing process, the hydrodimerization
of 1,3-butadiene.
DATES: Written comments on the petitioner's environmental assessment by
June 27, 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: Rosalie M. Angeles, Center for Food
Safety and Applied Nutrition (HFS-207), Food and Drug Administration,
200 C St. SW., Washington, DC 20204, 202-254-9528.
SUPPLEMENTARY INFORMATION: Under the Federal Food, Drug, and Cosmetic
Act (secs. 201(s), 409(b)(5) (21 U.S.C. 321(s), 348(b)(5))), notice is
given that a food additive petition (FAP 4A4419) has been filed by
Kuraray International Corp., c/o 1001 G St. NW., Washington, DC 20001.
The petition proposes that the food additive regulations in
Sec. 172.864 Synthetic fatty alcohols (21 CFR 172.864) be amended to
provide for the safe use of n-octanol produced by a new manufacturing
process, the hydrodimerization of 1,3-butadiene.
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
27, 1994, 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: May 18, 1994.
Fred R. Shank,
Director, Center for Food Safety and Applied Nutrition.
[FR Doc. 94-12855 Filed 5-25-94; 8:45 am]
BILLING CODE 4160-01-F
