Rodenticides; Proposed Risk Mitigation Decision; Extension of Comment Period, 11871-11872 [E7-4648]
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Federal Register / Vol. 72, No. 49 / Wednesday, March 14, 2007 / Notices
through use of products, and the general
protection of the environment and
special ecosystems from potential risks
posed by pesticides. The PPDC was
established under the Federal Advisory
Committee Act (FACA), Public Law 92463, in September 1995 for a 2 year–
term and has been renewed every 2
years since that time. The PPDC
provides advice and recommendations
to OPP on a broad range of pesticide
regulatory, policy, and program
implementation issues that are
associated with evaluating and reducing
risks from the use of pesticides. The
following sectors are represented on the
PPDC: Pesticide industry and trade
associations; environmental/public
interest and consumer groups; farm
worker organizations; pesticide user,
grower and commodity groups; Federal
and State/local/Tribal governments; the
general public; academia; and public
health organizations. Copies of the
PPDC charter are filed with appropriate
committees of Congress and the Library
of Congress and are available upon
request.
III. How Can I Request to Participate in
this Meeting?
This meeting will be open to the
public and seating is available on a firstcome basis. Persons interested in
attending do not need to register in
advance of the meeting. Opportunity
will be provided for questions and
comments by the public. Any person
who wishes to file a written statement
may do so before or after the meeting by
giving a copy of the statement to the
person listed under FOR FURTHER
INFORMATION CONTACT. These statements
will become part of the permanent
record and will be available for public
inspection at the address listed under
Unit 1.B.1. Do not submit any
information in your request that is
considered CBI.
To request accommodation of a
disability, please contact the person
listed under FOR FURTHER INFORMATION
CONTACT, preferably at least 10 days
prior to the meeting, to give EPA as
much time as possible to process your
request.
cprice-sewell on PROD1PC66 with NOTICES
List of Subjects
Environmental protection.
Dated: March 7, 2007.
James Jones,
Director, Office of Pesticide Programs.
[FR Doc. E7–4647 Filed 3–13–07 8:45 am]
BILLING CODE 6560–50–S
VerDate Aug<31>2005
15:03 Mar 13, 2007
Jkt 211001
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2006–0955-FRL–8119–1]
Rodenticides; Proposed Risk
Mitigation Decision; Extension of
Comment Period
Environmental Protection
Agency (EPA).
ACTION: Notice; extension of comment
period.
AGENCY:
SUMMARY: EPA issued a notice in the
Federal Register of January 17, 2007,
concerning the availability of the
Proposed Risk Mitigation Decision for
nine rodenticides. The nine
rodenticides covered by the Proposed
Risk Mitigation Decision are
brodifacoum, bromadiolone,
difethialone, chlorophacinone,
diphacinone, warfarin, zinc phosphide,
bromethalin, and cholecalciferol. This
document is extending the comment
period for 60 days, from March 19,
2007, to May 18, 2007.
DATES: Comments, identified by docket
identification (ID) number EPA–HQ–
OPP–2006–0955, must be received on or
before May 18, 2007.
ADDRESSES: Follow the detailed
instructions as provided under
ADDRESSES in the Federal Register
document of January 17, 2007.
FOR FURTHER INFORMATION CONTACT:
Kelly Sherman, Special Review and
Reregistration Division (7508P), Office
of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001;
telephone number: (703) 305-8401; email address: sherman.kelly@epa.gov or
Laura Parsons, Special Review and
Reregistration Division (7508P), Office
of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001;
telephone number: (703) 305-5776; email address: parsons.laura@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
The Agency included in the notice a
list of those who may be potentially
affected by this action. If you have
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
B. What Should I Consider as I Prepare
My Comments for EPA?
1. Submitting CBI. Do not submit this
information to EPA through
regulations.gov or e-mail. Clearly mark
the part or all of the information that
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11871
you claim to be CBI. For CBI
information in a disk or CD ROM that
you mail to EPA, mark the outside of the
disk or CD ROM as CBI and then
identify electronically within the disk or
CD ROM the specific information that is
claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2.
2. Tips for preparing your comments.
When submitting comments, remember
to:
i. Identify the document by docket ID
number and other identifying
information (subject heading, Federal
Register date and page number).
ii. Follow directions. The Agency may
ask you to respond to specific questions
or organize comments by referencing a
Code of Federal Regulations (CFR) part
or section number.
iii. Explain why you agree or disagree;
suggest alternatives and substitute
language for your requested changes.
iv. Describe any assumptions and
provide any technical information and/
or data that you used.
v. If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
vi. Provide specific examples to
illustrate your concerns and suggest
alternatives.
vii. Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
viii. Make sure to submit your
comments by the comment period
deadline identified.
C. How and to Whom Do I Submit
Comments?
To submit comments, or access the
official public docket, please follow the
detailed instructions as provided in
SUPPLEMENTARY INFORMATION of the
January 17, 2007, Federal Register
document. If you have questions,
consult the person listed under FOR
FURTHER INFORMATION CONTACT.
II. What Action is EPA Taking?
This document extends the public
comment period established in the
Federal Register of January 17, 2007 (72
FR 1992) (FRL–8104–7). In that
document, EPA announced the
availability of the availability of the
Proposed Risk Mitigation Decision for
nine rodenticides. The nine
rodenticides covered by the Proposed
E:\FR\FM\14MRN1.SGM
14MRN1
11872
Federal Register / Vol. 72, No. 49 / Wednesday, March 14, 2007 / Notices
Risk Mitigation Decision are
brodifacoum, bromadiolone,
difethialone, chlorophacinone,
diphacinone, warfarin, zinc phosphide,
bromethalin, and cholecalciferol. EPA is
hereby extending the comment period,
which was set to end on March 19,
2007, to May 18, 2007.
III. What is the Agency’s Authority for
Taking this Action?
Section 4(g)(2) of FIFRA, as amended,
directs that, after submission of all data
concerning a pesticide active ingredient,
the Administrator shall determine
whether pesticides containing such
active ingredient are eligible for
reregistration. Further provisions are
made to allow a public comment period.
However, the Administrator may extend
the comment period, if additional time
for comment is requested. In this case,
several stakeholders have requested
additional time to develop comments
due to the complexity of the issues
raised by the proposed mitigation
decision. In addition, the Rodenticide
Registrants Task Force (RRTF) has
requested additional time to develop
comments using information recently
placed in the docket and provided to the
RRTF.
List of Subjects
Environmental protection, Pesticides
and Pests.
Dated: March 2, 2007.
Debra Edwards,
Director, Special Review and Reregistration,
Division, Office of Pesticide Programs]
[FR Doc. E7–4648 Filed 3–13–07; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2007–0168; FRL–8117–8]
Pesticide Product Registrations;
Conditional Approval – Beauveria
bassiana HF23
Environmental Protection
Agency (EPA).
ACTION: Notice.
cprice-sewell on PROD1PC66 with NOTICES
AGENCY:
SUMMARY: This notice announces
Agency approval of applications
submitted by Jabb of the Carolinas, to
conditionally register the pesticide
products Beauveria bassiana HF23
(Technical) and the End-use Product,
balEnce containing a new active
ingredient not included in any
previously registered products pursuant
to the provisions of section 3(c)(7)(C) of
the Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA), as amended.
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FOR FURTHER INFORMATION CONTACT:
Shanaz Bacchus, Biopesticides and
Pollution Prevention Division (7511P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460-0001; telephone number:
(703) 308-8097; e-mail address:
bacchus.shanaz@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. Potentially
affected entities may include, but are
not limited to:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
assist you and others in determining
whether this action might apply to
certain entities. To determine whether
you or your business may be affected by
this action, you should carefully
examine the applicability provisions. If
you have any questions regarding the
applicability of this action to a
particular entity, consult the person
listed under FOR FURTHER INFORMATION
CONTACT.
B. How Can I Get Copies of this
Document and Other Related
Information?
1. Docket. EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPPT–2007–0168. Publicly available
docket materials are available either in
the electronic docket at https://
www.regulations.gov, or, if only
available in hard copy, at the Office of
Pesticide Programs (OPP) Regulatory
Public Docket in Rm. S-4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. The hours of
operation of this Docket Facility are
from 8:30 a.m. to 4 p.m., Monday
through Friday, excluding legal
holidays. The Docket telephone number
is (703) 305-5805.
In accordance with section 3(c)(2) of
FIFRA, a copy of the approved label, the
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list of data references, the data and other
scientific information used to support
registration, except for material
specifically protected by section 10 of
FIFRA, are also available for public
inspection. Requests for data must be
made in accordance with the provisions
of the Freedom of Information Act and
must be addressed to the Freedom of
Information Office (A-101), 1200
Pennsylvania Ave., NW., Washington,
DC 20460-0001. Such requests should:
Identify the product name and
registration number and specify the data
or information desired.
A paper copy of the fact sheet, which
provides more detail on this
registration, may be obtained from the
National Technical Information Service
(NTIS), 5285 Port Royal Rd.,
Springfield, VA 22161.
2. Electronic access. You may access
this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr.
II. Did EPA Conditionally Approve the
Application?
A conditional registration may be
granted under section 3(c)(7)(C) of
FIFRA for a new active ingredient where
certain data are lacking, on condition
that such data are received by the end
of the conditional registration period
and do not meet or exceed the risk
criteria set forth in 40 CFR 154.7; that
use of the pesticide during the
conditional registration period will not
cause unreasonable adverse effects; and
that use of the pesticide is in the public
interest. The Agency has considered the
available data on the risks associated
with the proposed use of Beauveria
bassiana HF23, and information on
social, economic, and environmental
benefits to be derived from such use.
Specifically, the Agency has considered
the nature and its pattern of use,
application methods and rates, and level
and extent of potential exposure. Based
on these reviews, the Agency was able
to make basic health and safety
determinations which show that use of
Beauveria bassiana HF23 during the
period of conditional registration will
not cause any unreasonable adverse
effect on the environment, and that use
of the pesticide is, in the public interest.
Consistent with section 3(c)(7)(C) of
FIFRA, the Agency has determined that
these conditional registrations are in the
public interest. Use of the pesticides are
of significance to the user community,
and appropriate labeling, use directions,
and other measures have been taken to
ensure that use of the pesticides will not
result in unreasonable adverse effects to
man and the environment.
E:\FR\FM\14MRN1.SGM
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Agencies
[Federal Register Volume 72, Number 49 (Wednesday, March 14, 2007)]
[Notices]
[Pages 11871-11872]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-4648]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2006-0955-FRL-8119-1]
Rodenticides; Proposed Risk Mitigation Decision; Extension of
Comment Period
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice; extension of comment period.
-----------------------------------------------------------------------
SUMMARY: EPA issued a notice in the Federal Register of January 17,
2007, concerning the availability of the Proposed Risk Mitigation
Decision for nine rodenticides. The nine rodenticides covered by the
Proposed Risk Mitigation Decision are brodifacoum, bromadiolone,
difethialone, chlorophacinone, diphacinone, warfarin, zinc phosphide,
bromethalin, and cholecalciferol. This document is extending the
comment period for 60 days, from March 19, 2007, to May 18, 2007.
DATES: Comments, identified by docket identification (ID) number EPA-
HQ-OPP-2006-0955, must be received on or before May 18, 2007.
ADDRESSES: Follow the detailed instructions as provided under
ADDRESSES in the Federal Register document of January 17, 2007.
FOR FURTHER INFORMATION CONTACT: Kelly Sherman, Special Review and
Reregistration Division (7508P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: (703) 305-8401; e-mail
address: sherman.kelly@epa.gov or Laura Parsons, Special Review and
Reregistration Division (7508P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: (703) 305-5776; e-mail
address: parsons.laura@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
The Agency included in the notice a list of those who may be
potentially affected by this action. If you have questions regarding
the applicability of this action to a particular entity, consult the
person listed under FOR FURTHER INFORMATION CONTACT.
B. What Should I Consider as I Prepare My Comments for EPA?
1. Submitting CBI. Do not submit this information to EPA through
regulations.gov or e-mail. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD ROM that you mail to EPA, mark the outside of the disk or CD ROM as
CBI and then identify electronically within the disk or CD ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
2. Tips for preparing your comments. When submitting comments,
remember to:
i. Identify the document by docket ID number and other identifying
information (subject heading, Federal Register date and page number).
ii. Follow directions. The Agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section number.
iii. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
iv. Describe any assumptions and provide any technical information
and/or data that you used.
v. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
vi. Provide specific examples to illustrate your concerns and
suggest alternatives.
vii. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
viii. Make sure to submit your comments by the comment period
deadline identified.
C. How and to Whom Do I Submit Comments?
To submit comments, or access the official public docket, please
follow the detailed instructions as provided in SUPPLEMENTARY
INFORMATION of the January 17, 2007, Federal Register document. If you
have questions, consult the person listed under FOR FURTHER INFORMATION
CONTACT.
II. What Action is EPA Taking?
This document extends the public comment period established in the
Federal Register of January 17, 2007 (72 FR 1992) (FRL-8104-7). In that
document, EPA announced the availability of the availability of the
Proposed Risk Mitigation Decision for nine rodenticides. The nine
rodenticides covered by the Proposed
[[Page 11872]]
Risk Mitigation Decision are brodifacoum, bromadiolone, difethialone,
chlorophacinone, diphacinone, warfarin, zinc phosphide, bromethalin,
and cholecalciferol. EPA is hereby extending the comment period, which
was set to end on March 19, 2007, to May 18, 2007.
III. What is the Agency's Authority for Taking this Action?
Section 4(g)(2) of FIFRA, as amended, directs that, after
submission of all data concerning a pesticide active ingredient, the
Administrator shall determine whether pesticides containing such active
ingredient are eligible for reregistration. Further provisions are made
to allow a public comment period. However, the Administrator may extend
the comment period, if additional time for comment is requested. In
this case, several stakeholders have requested additional time to
develop comments due to the complexity of the issues raised by the
proposed mitigation decision. In addition, the Rodenticide Registrants
Task Force (RRTF) has requested additional time to develop comments
using information recently placed in the docket and provided to the
RRTF.
List of Subjects
Environmental protection, Pesticides and Pests.
Dated: March 2, 2007.
Debra Edwards,
Director, Special Review and Reregistration, Division, Office of
Pesticide Programs]
[FR Doc. E7-4648 Filed 3-13-07; 8:45 am]
BILLING CODE 6560-50-S