Danisco USA, Inc.; Filing of Food Additive Petition, 7975 [E6-2130]
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Federal Register / Vol. 71, No. 31 / Wednesday, February 15, 2006 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Food and Drug Administration
[Docket No. 2006F–0059]
[Docket No. 2006F–0058]
ARCH Chemicals, Inc.; Filing of Food
Additive Petition
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
AGENCY:
Notice.
FOR FURTHER INFORMATION CONTACT:
Elizabeth R. Sanchez, Center for Food
Safety and Applied Nutrition (HFS 275),
Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD
20740–3835, 301–436–1239.
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 6B4764) has been filed by
ARCH Chemicals, Inc., 1955 Lake Park
Dr., suite 100, Smyrna, GA 30080. The
petition proposes to amend the food
additive regulations in § 176.170
Components of paper and paperboard
in contact with aqueous and fatty foods
and § 176.180 Components of paper and
paperboard in contact with dry food to
provide for the safe use of poly
(iminoimidocarbonyliminoimidocarbonyliminohexamethylene)
hydrochloride (CAS Reg. No. 32289–58–
0) as an antimicrobial agent in the
manufacture of food-contact paper and
paperboard.
The agency has determined under 21
CFR 25.32(q) that this action is of a type
that does not individually or
cumulatively have a significant effect on
the human environment. Therefore,
neither an environmental assessment
nor an environmental impact statement
is required.
SUPPLEMENTARY INFORMATION:
Dated: January 25, 2006.
Laura M. Tarantino,
Director, Office of Food Safety, Center for
Food Safety and Applied Nutrition.
[FR Doc. E6–2137 Filed 2–14–06; 8:45 am]
BILLING CODE 4160–01–S
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Jkt 208001
Food and Drug Administration,
HHS.
ACTION:
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that ARCH Chemicals, Inc., has filed a
petition proposing that the food additive
regulations be amended to provide for
the safe use of poly
(iminoimidocarbonyliminoimidocarbonyliminohexamethylene)
hydrochloride (CAS Reg. No. 32289–58–
0) as an antimicrobial agent in the
manufacture of food-contact paper and
paperboard.
cprice-sewell on PROD1PC66 with NOTICES
Danisco USA, Inc.; Filing of Food
Additive Petition
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that Danisco USA, Inc., has filed a
petition proposing that the food additive
regulations be amended to provide for
the safe use of polydextrose as a bulking
agent, formulation aid, humectant and
texturizer in all foods, except meat and
poultry.
DATES: Submit written or electronic
comments on the petitioner’s
environmental assessment by March 17,
2006.
ADDRESSES: Submit written comments
to the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments to https://
www.fda.gov/dockets/ecomments.
FOR FURTHER INFORMATION CONTACT: Paul
C. DeLeo, Center for Food Safety and
Applied Nutrition (HFS–265), Food and
Drug Administration, 5100 Paint Branch
Pkwy., College Park, MD 20740–3835,
301–436–1302.
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 6A4763) has been filed by
Danisco USA, Inc., 440 Saw Mill River
Rd., Ardsley, NY 10502–2605. The
petition proposes to amend the food
additive regulations in § 172.841
Polydextrose (21 CFR 172.841) to
provide for the safe use of polydextrose
as a bulking agent, formulation aid,
humectant, and texturizer in all foods,
except meat and poultry. The proposed
amendment would consolidate all
existing food use categories and permit
additional uses not allowed by the
existing regulation.
The potential environmental impact
of this action is being reviewed. To
encourage public participation
consistent with regulations issued 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 Division of Dockets Management
(see ADDRESSES) for public review and
PO 00000
Frm 00064
Fmt 4703
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7975
comment. Interested persons may
submit to the Division of Dockets
Management written or electronic
comments by March 17, 2006. Two
copies of any written 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 Division of Dockets
Management 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 25.51(b).
Dated: January 25, 2006.
Laura M. Tarantino,
Director, Office of Food Additive Safety,
Center for Food Safety and Applied Nutrition.
[FR Doc. E6–2130 Filed 2–14–06; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005D–0505]
Guidance for Industry and Food and
Drug Administration; Class II Special
Controls Guidance Document:
Implantable Intra-Aneurysm Pressure
Measurement System; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of the guidance entitled
‘‘Class II Special Controls Guidance
Document: Implantable Intra-Aneurysm
Pressure Measurement System.’’ This
guidance document describes a means
by which the implantable intraaneurysm pressure measurement system
may comply with the requirement of
special controls for class II devices.
Elsewhere in this issue of the Federal
Register, FDA is publishing a final rule
to classify these device types into class
II (special controls). This guidance
document is immediately in effect as the
special control for implantable intraaneurysm pressure measurement
E:\FR\FM\15FEN1.SGM
15FEN1
Agencies
[Federal Register Volume 71, Number 31 (Wednesday, February 15, 2006)]
[Notices]
[Page 7975]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-2130]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006F-0059]
Danisco USA, Inc.; Filing of Food Additive Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that
Danisco USA, Inc., has filed a petition proposing that the food
additive regulations be amended to provide for the safe use of
polydextrose as a bulking agent, formulation aid, humectant and
texturizer in all foods, except meat and poultry.
DATES: Submit written or electronic comments on the petitioner's
environmental assessment by March 17, 2006.
ADDRESSES: Submit written comments to the Division of Dockets
Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane,
rm. 1061, Rockville, MD 20852. Submit electronic comments to https://
www.fda.gov/dockets/ecomments.
FOR FURTHER INFORMATION CONTACT: Paul C. DeLeo, Center for Food Safety
and Applied Nutrition (HFS-265), Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD 20740-3835, 301-436-1302.
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 6A4763) has been filed by Danisco USA, Inc., 440
Saw Mill River Rd., Ardsley, NY 10502-2605. The petition proposes to
amend the food additive regulations in Sec. 172.841 Polydextrose (21
CFR 172.841) to provide for the safe use of polydextrose as a bulking
agent, formulation aid, humectant, and texturizer in all foods, except
meat and poultry. The proposed amendment would consolidate all existing
food use categories and permit additional uses not allowed by the
existing regulation.
The potential environmental impact of this action is being
reviewed. To encourage public participation consistent with regulations
issued 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
Division of Dockets Management (see ADDRESSES) for public review and
comment. Interested persons may submit to the Division of Dockets
Management written or electronic comments by March 17, 2006. Two copies
of any written 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 Division of Dockets Management 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 25.51(b).
Dated: January 25, 2006.
Laura M. Tarantino,
Director, Office of Food Additive Safety, Center for Food Safety and
Applied Nutrition.
[FR Doc. E6-2130 Filed 2-14-06; 8:45 am]
BILLING CODE 4160-01-S