Tralomethrin and Fenarimol Registration Review Final Decisions; Notice of Availability, 69839-69840 [2012-28213]
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Federal Register / Vol. 77, No. 225 / Wednesday, November 21, 2012 / Notices
in the proposed EUP include
Cry1A.105, Cry2Ab2, Cry IF, Vip3Aa20,
Cry3Bb1, Cry34Abl/Cry35Abl and
eCry3.1Ab. The environmental and
human health safety of these proteins
has been demonstrated, and they are
exempted from the requirement of a
tolerance (40 CFR 174.501, 174.502,
174.506, 174.518, 174.519, 174.520,
174.528, 174.532). A permanent
tolerance exemption has been
established for nucleic acids including
the dsRNA that is part of the PIPs (40
CFR 174.507). Other marker proteins
PAT, CP4 EPSPS, and PMI are also
exempt from the requirement of a
tolerance (40 CFR 174.522, 174.523,
174.527).
The tests will be conducted in the
U.S. territory of Puerto Rico and in the
U.S. in twenty two (22) states as follows:
Arkansas (AR), California (CA),
Colorado (CO), Georgia (GA), Hawaii
(HI), Idaho (ID), Illinois (IL), Indiana
(IN), Iowa (IA), Kansas (KS), Michigan
(MI), Minnesota (MN), Mississippi (MS),
Missouri (MO), Nebraska (NE), North
Carolina (NC), Ohio (OH), Pennsylvania
(PA), South Carolina (SC), South Dakota
(SD), Tennessee (TN), Wisconsin (WI).
The two protocols in the EUP include:
(1) Seed development and increase for
future testing including nursery
observations of traits in various genetic
backgrounds; and (2) product
characterization work including
phenotypic and agronomic observations,
efficacy, yield benefit evaluations and
regulatory data generation.
A copy of the application and any
information submitted is available for
public review in the docket established
for this EUP application.
Following the review of the
application and any comments and data
received in response to this solicitation,
EPA will decide whether to issue or
deny the EUP request, and if issued, the
conditions under which it is to be
conducted. Any issuance of an EUP will
be announced in the Federal Register.
List of Subjects
srobinson on DSK4SPTVN1PROD with
Dated: November 8, 2012,
Keith Matthews,
Director, Biopesticides and Pollution
Prevention Division, Office of Pesticide
Programs.
[FR Doc. 2012–28215 Filed 11–20–12; 8:45 am]
BILLING CODE 6560–50–P
16:56 Nov 20, 2012
[EPA–HQ–OPP–2012–0425; FRL–9368–9]
Tralomethrin and Fenarimol
Registration Review Final Decisions;
Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of EPA’s final registration
review decision for the pesticides
tralomethrin and fenarimol. Registration
review is EPA’s periodic review of
pesticide registrations to ensure that
each pesticide continues to satisfy the
statutory standard for registration, that
is, that the pesticide can perform its
intended function without causing
unreasonable adverse effects on human
health or the environment. Through this
program, EPA is ensuring that each
pesticide’s registration is based on
current scientific and other knowledge,
including its effects on human health
and the environment.
FOR FURTHER INFORMATION CONTACT: For
pesticide specific information, contact:
Wilhelmena Livingston (tralomethrin),
telephone number: (703) 308–8025; fax
number: (703) 308–8005; email address:
livingston.wilhelmena@epa.gov, or
Garland Waleko (fenarimol), telephone
number: (703) 308–8049; fax number:
(703) 308–8005; email address:
waleko.garland@epa.gov., Pesticide Reevaluation Division (7508P), Office of
Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460–
0001.
For general information on the
registration review program, contact:
Kevin Costello, Pesticide Re-evaluation
Division (7508P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460–0001; telephone
number: (703) 305–5026; fax number:
(703) 308–8005; email address:
costello.kevin@epa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. General Information
Environmental protection,
Experimental use permits.
VerDate Mar<15>2010
ENVIRONMENTAL PROTECTION
AGENCY
Jkt 229001
A. Does this action apply to me?
This action is directed to the public
in general, and may be of interest to a
wide range of stakeholders including
environmental, human health, farm
worker and agricultural advocates; the
chemical industry; pesticide users; and
members of the public interested in the
sale, distribution, or use of pesticides.
Since others also may be interested, the
Agency has not attempted to describe all
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
69839
the specific entities that may be affected
by this action. If you have any questions
regarding the applicability of this action
to a particular entity, consult the
pesticide specific contact person listed
under FOR FURTHER INFORMATION
CONTACT.
B. How can I get copies of this document
and other related information?
The docket for this action, identified
by docket identification (ID) number
EPA–HQ–OPP–2012–0425, is available
at https://www.regulations.gov or at the
Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the
Environmental Protection Agency
Docket Center (EPA/DC), EPA West
Bldg., Rm. 3334, 1301 Constitution Ave.
NW., Washington, DC 20460–0001. The
Public Reading Room is open from 8:30
a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The
telephone number for the Public
Reading Room is (202) 566–1744, and
the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
II. Background
A. What action is the agency taking?
Pursuant to 40 CFR 155.58(c), this
notice announces the availability of
EPA’s registration review final decisions
for tralomethrin, Case Number 7400,
and fenarimol, Case Number 7001.
Tralomethrin was a broad-spectrum
Type II systemic pyrethroid ester
insecticide that was registered for use in
a variety of residential and commercial
settings, and on a small number of
agricultural crops including broccoli,
cauliflower, cotton, lettuce, peanuts,
and sunflowers. Tralomethrin technical
was cancelled in a product cancellation
order issued in the Federal Register of
February 25, 2011. The effective date of
the cancellation is February 25, 2011 (76
FR 10587, February 25, 2011).
Fenarimol is a member of the
pyrimidine class of fungicides used for
control of such pests as scab, powdery
mildew, rusts, and leaf spot. Fenarimol
inhibits fungal growth by adversely
affecting the formation of the fungal
sterol ergosterol, and is currently
registered for use on fruit and nut crops
such as apples, cherries, filberts
(nonbearing), grapes, hops, pears, and
pecans, as well as on ornamental plants,
trees, and grasses and turf lawns. The
fenarimol technical and end use
products are voluntarily canceled as of
July 31, 2013.
Pursuant to 40 CFR 155.57, a
registration review decision is the
E:\FR\FM\21NON1.SGM
21NON1
69840
Federal Register / Vol. 77, No. 225 / Wednesday, November 21, 2012 / Notices
Agency’s determination whether a
pesticide meets, or does not meet, the
standard for registration in FIFRA. EPA
has considered tralomethrin and
fenarimol in light of the FIFRA standard
for registration. The tralomethrin and
fenarimol final decision documents in
the docket describe the Agency’s
rationale for issuing a registration
review final decision for these
pesticides.
In addition to the final registration
review decision documents, the
registration review docket for
tralomethrin and fenarimol also
includes other relevant documents
related to the registration review of
these cases. The proposed registration
review decisions were posted to the
docket and the public was invited to
submit any comments or new
information. During the 60-day
comment period, no public comments
were received. Pursuant to 40 CFR
155.58(c), the registration review case
docket for tralomethrin and fenarimol
will remain open until all actions
required in the final decision have been
completed.
Background on the registration review
program is provided at: https://
www.epa.gov/oppsrrd1/
registration_review. Links to earlier
documents related to the registration
review of these pesticides are provided
at: https://www.epa.gov/pesticides/
chemicalsearch/.
B. What is the agency’s authority for
taking this action?
Section 3(g) of FIFRA and 40 CFR part
155, subpart C, provide authority for
this action.
List of Subjects
Environmental protection,
Registration review, Pesticides and
pests, Tralomethrin and Fenarimol.
Dated: November 9, 2012.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2012–28213 Filed 11–20–12; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
srobinson on DSK4SPTVN1PROD with
Iodomethane; Notice of Receipt of
Request to Voluntarily Cancel
Iodomethane Pesticide Registrations
and Amend a Registration
Environmental Protection
Agency (EPA).
ACTION: Notice.
VerDate Mar<15>2010
16:56 Nov 20, 2012
Jkt 229001
Comments must be received on
or before December 21, 2012.
DATES:
Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2005–0252, by
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW., Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.htm.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
[EPA–HQ–OPP–2005–0252; FRL–9370–2]
AGENCY:
In accordance with the
Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA), EPA is issuing
a notice of receipt of a request by the
registrant to voluntarily cancel the
registrations of products containing the
pesticide iodomethane. In addition, the
registrant has amended the terms and
conditions of registration for their
iodomethane technical product so that
as of January 1, 2013, Arysta LifeScience
North America, LLC (Arysta) will not
sell or distribute this product unless it
bears a label statement. The registrant’s
request would terminate the last
iodomethane products registered for use
in the United States. EPA intends to
grant this request at the close of the
comment period for this announcement
unless the Agency receives substantive
comments within the comment period
that would merit its further review of
the request. If EPA issues a final order
granting this request, the sale,
distribution, or use of the products
listed in this notice will be permitted
only in accordance with the terms as
described in the final order.
SUMMARY:
Andrea Mojica, Pesticide Re-evaluation
Division (7508P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460–0001; telephone
number: (703) 308–0122; fax number:
(703) 308–8090; email address:
mojica.andrea@epa.gov.
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00052
Fmt 4703
Sfmt 4703
I. General Information
A. Does this action apply to me?
This action is directed to the public
in general, and may be of interest to a
wide range of stakeholders including
environmental, human health, and
agricultural advocates; the chemical
industry; pesticide users; and members
of the public interested in the sale,
distribution, or use of pesticides. Since
others also may be interested, the
Agency has not attempted to describe all
the specific entities that may be affected
by this action.
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 email. 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.
E:\FR\FM\21NON1.SGM
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Agencies
[Federal Register Volume 77, Number 225 (Wednesday, November 21, 2012)]
[Notices]
[Pages 69839-69840]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-28213]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2012-0425; FRL-9368-9]
Tralomethrin and Fenarimol Registration Review Final Decisions;
Notice of Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the availability of EPA's final
registration review decision for the pesticides tralomethrin and
fenarimol. Registration review is EPA's periodic review of pesticide
registrations to ensure that each pesticide continues to satisfy the
statutory standard for registration, that is, that the pesticide can
perform its intended function without causing unreasonable adverse
effects on human health or the environment. Through this program, EPA
is ensuring that each pesticide's registration is based on current
scientific and other knowledge, including its effects on human health
and the environment.
FOR FURTHER INFORMATION CONTACT: For pesticide specific information,
contact: Wilhelmena Livingston (tralomethrin), telephone number: (703)
308-8025; fax number: (703) 308-8005; email address:
livingston.wilhelmena@epa.gov, or Garland Waleko (fenarimol), telephone
number: (703) 308-8049; fax number: (703) 308-8005; email address:
waleko.garland@epa.gov., Pesticide Re-evaluation Division (7508P),
Office of Pesticide Programs, Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington, DC 20460-0001.
For general information on the registration review program,
contact: Kevin Costello, Pesticide Re-evaluation Division (7508P),
Office of Pesticide Programs, Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington, DC 20460-0001; telephone number:
(703) 305-5026; fax number: (703) 308-8005; email address:
costello.kevin@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public in general, and may be of
interest to a wide range of stakeholders including environmental, human
health, farm worker and agricultural advocates; the chemical industry;
pesticide users; and members of the public interested in the sale,
distribution, or use of pesticides. Since others also may be
interested, the Agency has not attempted to describe all the specific
entities that may be affected by this action. If you have any questions
regarding the applicability of this action to a particular entity,
consult the pesticide specific contact person listed under FOR FURTHER
INFORMATION CONTACT.
B. How can I get copies of this document and other related information?
The docket for this action, identified by docket identification
(ID) number EPA-HQ-OPP-2012-0425, is available at https://www.regulations.gov or at the Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the Environmental Protection Agency
Docket Center (EPA/DC), EPA West Bldg., Rm. 3334, 1301 Constitution
Ave. NW., Washington, DC 20460-0001. The Public Reading Room is open
from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal
holidays. The telephone number for the Public Reading Room is (202)
566-1744, and the telephone number for the OPP Docket is (703) 305-
5805. Please review the visitor instructions and additional information
about the docket available at https://www.epa.gov/dockets.
II. Background
A. What action is the agency taking?
Pursuant to 40 CFR 155.58(c), this notice announces the
availability of EPA's registration review final decisions for
tralomethrin, Case Number 7400, and fenarimol, Case Number 7001.
Tralomethrin was a broad-spectrum Type II systemic pyrethroid ester
insecticide that was registered for use in a variety of residential and
commercial settings, and on a small number of agricultural crops
including broccoli, cauliflower, cotton, lettuce, peanuts, and
sunflowers. Tralomethrin technical was cancelled in a product
cancellation order issued in the Federal Register of February 25, 2011.
The effective date of the cancellation is February 25, 2011 (76 FR
10587, February 25, 2011). Fenarimol is a member of the pyrimidine
class of fungicides used for control of such pests as scab, powdery
mildew, rusts, and leaf spot. Fenarimol inhibits fungal growth by
adversely affecting the formation of the fungal sterol ergosterol, and
is currently registered for use on fruit and nut crops such as apples,
cherries, filberts (nonbearing), grapes, hops, pears, and pecans, as
well as on ornamental plants, trees, and grasses and turf lawns. The
fenarimol technical and end use products are voluntarily canceled as of
July 31, 2013.
Pursuant to 40 CFR 155.57, a registration review decision is the
[[Page 69840]]
Agency's determination whether a pesticide meets, or does not meet, the
standard for registration in FIFRA. EPA has considered tralomethrin and
fenarimol in light of the FIFRA standard for registration. The
tralomethrin and fenarimol final decision documents in the docket
describe the Agency's rationale for issuing a registration review final
decision for these pesticides.
In addition to the final registration review decision documents,
the registration review docket for tralomethrin and fenarimol also
includes other relevant documents related to the registration review of
these cases. The proposed registration review decisions were posted to
the docket and the public was invited to submit any comments or new
information. During the 60-day comment period, no public comments were
received. Pursuant to 40 CFR 155.58(c), the registration review case
docket for tralomethrin and fenarimol will remain open until all
actions required in the final decision have been completed.
Background on the registration review program is provided at:
https://www.epa.gov/oppsrrd1/registration_review. Links to earlier
documents related to the registration review of these pesticides are
provided at: https://www.epa.gov/pesticides/chemicalsearch/.
B. What is the agency's authority for taking this action?
Section 3(g) of FIFRA and 40 CFR part 155, subpart C, provide
authority for this action.
List of Subjects
Environmental protection, Registration review, Pesticides and
pests, Tralomethrin and Fenarimol.
Dated: November 9, 2012.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2012-28213 Filed 11-20-12; 8:45 am]
BILLING CODE 6560-50-P