[Federal Register Volume 61, Number 141 (Monday, July 22, 1996)]
[Notices]
[Pages 37905-37906]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-18439]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 96F-0248]
Life Technologies, 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 Life
Technologies, Inc., has filed a
[[Page 37906]]
petition proposing that the food additive regulations be amended to
provide for a change in the limitations for sulphopropyl cellulose ion-
exchange resin for the recovery and purification of proteins for food
use.
DATES: Written comments on the petitioner's environmental assessment by
August 21, 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: Andrew D. Laumbach, -Center for Food
Safety and Applied Nutrition (HFS-217), Food and Drug Administration,
200 C St. SW., Washington, DC 20204, 202-418-3071.
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 6A4502) has been filed by Life Technologies,
Inc., 8400 Helgerman Ct., Gaithersburg, MD 20874. The petition proposes
to amend the food additive regulations in Sec. 173.25(b)(5) Ion-
exchange resins (21 CFR 173.25(b)(5)) to provide for a change in the
temperature and pH limitations for sulphopropyl cellulose ion-exchange
resin for the recovery and purification of proteins for food use.
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 August
21, 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: July 10, 1996.
George H. Pauli,
Acting Director, Office of Premarket Approval, Center for Food Safety
and Applied Nutrition.
[FR Doc. 96-18439 Filed 7-19-96; 8:45 am]
BILLING CODE 4160-01-F
