[Federal Register Volume 62, Number 186 (Thursday, September 25, 1997)]
[Notices]
[Page 50387]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-25368]
[[Page 50387]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 97F-0388]
Cultor Food Science, Inc.; Filing of Food Additive Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that
Cultor Food Science, Inc., has filed a petition proposing that the food
additive regulations be amended to permit aqueous transition metal
catalytic hydrogenation in the production of polydextrose and to adopt
the specifications for polydextrose of the Food Chemicals Codex, 4th
ed., 1996.
DATES: Written comments on the petitioner's environmental assessment by
October 27, 1997.
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: Rosalie M. Angeles, Center for Food
Safety and Applied Nutrition (HFS-206), Food and Drug Administration,
200 C St. SW., Washington, DC 20204, 202-418-3107.
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 7A4556) has been filed by Cultor Food Science,
Inc., 205 East 42d St., New York, NY 10017. The petition proposes to
amend the food additive regulations in Sec. 172.841 Polydextrose (21
CFR 172.841) to permit aqueous transition metal catalytic hydrogenation
in the production of polydextrose and to adopt the specifications for
polydextrose of the Food Chemicals Codex, 4th ed., 1996, pp. 297-300.
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 October
27, 1997 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: September 9, 1997.
Alan M. Rulis,
Director, Office of Premarket Approval, Center for Food Safety and
Applied Nutrition.
[FR Doc. 97-25368 Filed 9-24-97; 8:45 am]
BILLING CODE 4160-01-F