Difenzoquat; Data Call-in Order for Pesticide Tolerances, 75037-75039 [2012-30617]
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Federal Register / Vol. 77, No. 244 / Wednesday, December 19, 2012 / Rules and Regulations
75037
AIR POLLUTION CONTROL REGULATIONS FOR SOUTH CAROLINA—Continued
State
effective date
State citation
Title/subject
Section 8–13–730 ...........................................
Membership on or employment by regulatory
agency of person associated with regulated business.
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[FR Doc. 2012–30437 Filed 12–18–12; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2012–0441; FRL–9372–9]
Difenzoquat; Data Call-in Order for
Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final order.
AGENCY:
This order requires the
submission of various data to support
the continuation of the tolerances for
the pesticide, difenzoquat. Pesticide
tolerances are established under the
Federal Food, Drug, and Cosmetic Act
(FFDCA). Following publication of this
order, persons who are interested in the
continuation of the difenzoquat
tolerances must notify the Agency by
completing and submitting the required
section 408(f) Order Response Form
(available in the docket) within 90 days.
If the Agency does not receive within 90
days after publication of the final order
a section 408(f) Response Form
identifying a person who agrees to
submit the required data, EPA will
revoke the difenzoquat tolerances.
DATES: This final order is effective
December 19, 2012. A section 408(f)
Order Response Form must be received
on or before March 19, 2013.
ADDRESSES: EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPP–2012–0441. All documents in the
docket are listed in the docket index
available at https://www.regulations.gov.
Although listed in the index, some
information is not publicly available,
e.g., Confidential Business Information
(CBI) or other information whose
disclosure is restricted by statute.
Certain other material, such as
copyrighted material, is not placed on
the Internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available in the electronic docket at
https://www.regulations.gov, or, if only
wreier-aviles on DSK5TPTVN1PROD with
SUMMARY:
VerDate Mar<15>2010
15:12 Dec 18, 2012
Jkt 229001
available in hard copy, at the OPP
Regulatory Public 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.
Submit your section 408(f) Order
Response Form, identified by docket
identification (ID) number EPA–HQ–
OPP–2012–0441, by one of the
following methods:
• Federal eRulemaking Portal: Follow
the on-line instructions for submitting
comments.
• 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.
FOR FURTHER INFORMATION CONTACT:
Christina Scheltema, Pesticide Reevaluation Division (7508P), Office of
Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW., Washington, DC 20460–0001;
telephone number: (703) 308–2201;
email address:
scheltema.christina@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).
PO 00000
Frm 00031
Fmt 4700
Sfmt 4700
EPA
approval date
Federal Register notice
1/1/1992
8/1/2012
77 FR 45492
• 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. 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 electronic access to
other related information?
You may access a frequently updated
electronic version of 40 CFR part 180
through the Government Printing
Office’s e-CFR site at https://
ecfr.gpoaccess.gov/cgi/t/text/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl. To access the harmonized
test guidelines referenced in this
document electronically, please go to
https://www.epa.gov/ocspp and select
‘‘Test Methods and Guidelines,’’ which
is listed under ‘‘Documents related to
our mission.’’
II. Background
A. What action is the agency taking?
In this document EPA is issuing an
order requiring the submission of
various data to support the continuation
of the difenzoquat tolerances at 40 CFR
180.369, under section 408 of FFDCA,
21 U.S.C. 346a. Difenzoquat is not
currently registered under the Federal
Insecticide, Fungicide, and Rodenticide
Act (FIFRA), 7 U.S.C. 136 et seq. The
last FIFRA registration for difenzoquat
was canceled in 2010. However, 25
FFDCA tolerances remain for residues of
difenzoquat on the following
commodities: Barley, cattle, goat, hog,
horse, poultry, sheep, and wheat (40
CFR 180.369). Because there are
currently no domestic registrations for
difenzoquat, these tolerances are
referred to as ‘‘import tolerances.’’ It is
these tolerances that are addressed by
the Data Call-In order.
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75038
Federal Register / Vol. 77, No. 244 / Wednesday, December 19, 2012 / Rules and Regulations
B. What is the agency’s authority for
taking this action?
Under section 408(f) of the FFDCA,
EPA is authorized to require, by order,
submission of data ‘‘reasonably required
to support the continuation of a
tolerance’’ when such data cannot be
obtained under the Data Call-In
authority of FIFRA section 3(c)(2)(B), or
section 4 of the Toxic Substances
Control Act (‘‘TSCA’’), 15 U.S.C. 2603.
A FFDCA section 408 Data Call-In order
may only be issued following
publication of notice of the order and a
60-day public comment provision.
A section 408(f) Data Call-In order
must contain the following elements:
1. A requirement that one or more
persons submit to EPA a notice
identifying the person(s) who commit to
submit the data required in the order.
2. A description of the required data
and the required reports connected to
such data;
3. An explanation of why the required
data could not be obtained under
section 3(c)(2)(B) of FIFRA or section 4
of TSCA.
4. The required submission date for
the notice identifying one or more
interested persons who commit to
submit the required data and the
required submission dates for all the
data and reports required in the order
(21 U.S.C. 346a(f)(1)(C)).
EPA may by order modify or revoke
the affected tolerances if any one of the
following submissions is not made in a
timely manner:
1. A notice identifying the one or
more interested persons who commit to
submit the data.
2. The data itself.
3. The reports required under a
section 408(f) order are not submitted by
the date specified in the order (21 U.S.C.
346a(f)(2)).
C. What preliminary steps were taken by
EPA prior to issuing this final order?
On July 6, 2012 (77 FR 44181) (FRL–
9352–9), EPA issued a proposed Data
Call-In order for the pesticide
difenzoquat in connection with
tolerances for that pesticide under
section 408 of the Federal Food, Drug,
and Cosmetic Act (FFDCA), 21 U.S.C.
346a. The proposed Data Call-In order
included the following studies:
• Neurotoxicity Screening Battery
(870.6200).
• Immunotoxicity Study (870.7800).
• Crop Field Trials (860.1500)—
(wheat hay, wheat forage, and barley
hay).
III. Summary of Public Comments
Received and Agency Response to
Comments
EPA received no comments in
response to the July 6, 2012, Federal
Register notice announcing the
Agency’s proposed Data Call-In order
for difenzoquat. In addition, the Agency
has not received any of the data
identified in the proposed order as
needed to support the difenzoquat
tolerances.
IV. Final Data Call-in Order
Because no comments were submitted
on the proposal and the data
deficiencies identified in the proposed
order remain, EPA is issuing this final
Data Call-In order under FFDCA section
408(f)(1)(C) for difenzoquat in the same
form as the proposed order and for the
reasons set forth in that proposed order.
Specifically, this order:
1. Requires notice of intent to submit
data. A notice identifying the person or
persons who commit to submit the data
and reports in accordance with Unit
IV.2. must be submitted to EPA if any
person wishes to support the
difenzoquat tolerances. The notice must
be submitted on a section 408(f) Order
Response Form which is available in the
electronic docket, https://
www.regulations.gov, under docket ID
number EPA–HQ–OPP–2012–0441.
2. Establishes a deadline for
submission of notice identifying data
submitters. The notice described in Unit
IV.1., identifying data submitters, must
be submitted to and received by EPA on
or before March 19, 2013. Instructions
on methods for responding to this order
(referred to in this order as a ‘‘section
408(f) Order Response Form’’) are set
out under the ADDRESSES section above.
3. Describes data and reports required
to support continuation of the
difenzoquat tolerances, requires
submission of those data and reports,
and establishes deadlines for
submission. The table in this Unit
describes the data and reports required
to be submitted on difenzoquat under
this order and the deadlines for the
submission of each study and report.
The required submission date is
calculated from March 19, 2013. Thus,
for example, if EPA generally allows 12
months to complete a study, the
required submission date for such a
study under this order would be 15
months from the date of publication of
the order in the Federal Register.
Studies, study protocols, and reports
should be submitted to the person listed
under FOR FURTHER INFORMATION
CONTACT.
TABLE—DATA AND REPORTS REQUIRED TO BE SUBMITTED ON DIFENZOQUAT
OCSPP
harmonized guideline No.
Study title
Timeframe for protocol
report submission
870.6200 ...............................
870.7800 ...............................
860.1500 ...............................
Neurotoxicity Screening Battery ........................................
Immunotoxicity Study .........................................................
Crop Field Trials (wheat hay, wheat forage, and barley
hay).
Not Required .......................
6 months ..............................
Not Required .......................
wreier-aviles on DSK5TPTVN1PROD with
EPA provided a description of why
the required data could not be obtained
under section 3(c)(2)(B) of FIFRA or
section 4 of TSCA in the proposed order
and relies on that description in this
final order.
V. Failure to Submit Notice of Intent to
Submit Data or Data and Reports
If, by March 19, 2013 the Agency does
not receive a section 408(f) Order
Response Form identifying a person
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15:12 Dec 18, 2012
Jkt 229001
who agrees to submit the required data,
EPA will revoke the difenzoquat
tolerances at 40 CFR 180.369. Such
revocation is subject to the objection
and hearing procedure in FFDCA
section 408(g)(2) but the only material
issue in such a procedure is whether a
submission required by the order was
made in a timely fashion.
Additional events that may be the
basis for modification or revocation of
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Fmt 4700
Sfmt 4700
Timeframe for data
submission
March 19, 2015.
March 19, 2014.
March 19, 2015.
difenzoquat tolerances include, but are
not limited to the following:
1. No person submits on the required
schedule an acceptable protocol report
when such report is required to be
submitted to the Agency for review.
2. No person submits on the required
schedule acceptable data as required by
the final order.
E:\FR\FM\19DER1.SGM
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Federal Register / Vol. 77, No. 244 / Wednesday, December 19, 2012 / Rules and Regulations
VI. Statutory and Executive Order
Reviews
This action, which requires the
submission of data in support of
tolerances in accordance with FFDCA
section 408, is in the form of an order
and not a rule (21 U.S.C. 346a(f)(1)(C)).
Under the Administrative Procedures
Act (APA), orders are expressly
excluded from the definition of a rule (5
U.S.C. 551(4)). Accordingly, the
regulatory assessment requirements
imposed on a rulemaking do not apply
to this action, as explained further in
the following discussion.
A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
Because this order is not a ‘‘regulatory
action’’ as that term is defined in
Executive Order 12866 (58 FR 51735,
October 4, 1993), this action is not
subject to review by the Office of
Management and Budget (OMB) under
Executive Orders 12866 and 13563 (76
FR 3821, January 21, 2011).
B. Paperwork Reduction Act
This action does not impose
additional burdens that require approval
by OMB under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et
seq.). The information collection
activities associated with the order
requesting data from any party
interested in supporting certain
tolerances are already approved by OMB
under OMB Control No. 2070–0174, and
are identified by EPA ICR No. 2288.01.
Burden is defined at 5 CFR 1320.3(b).
Under the PRA, an Agency may not
conduct or sponsor, and a person is not
required to respond to a collection of
information that requires OMB approval
under PRA, unless it has been approved
by OMB and displays a currently valid
OMB control number. The OMB control
numbers for EPA’s regulations in title 40
of the CFR, after appearing in the
Federal Register, are listed in 40 CFR
part 9, and included on the related
collection instrument, or form, if
applicable.
wreier-aviles on DSK5TPTVN1PROD with
Since this order is not a rule under
the APA (5 U.S.C. 551(4)), and does not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.) do not apply.
VerDate Mar<15>2010
15:12 Dec 18, 2012
D. Unfunded Mandates Reform Act;
Executive Order 13132: Federalism; and
Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
VII. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq. does not apply
because this action is not a rule as that
term is defined in 5 U.S.C. 804(3).
This order requests data from any
party interested in supporting certain
tolerances and does not impose
obligations on any person or entity
including States or tribes; nor does this
action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of section
408(n)(4) of FFDCA. As such, the
Agency has determined that this action
will not have a substantial direct effect
on States or tribal governments, on the
relationship between the national
government and the States or tribal
governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, the Agency has determined
that Executive Order 13132 (64 FR
43255, August 10, 1999) and Executive
Order 13175 (65 FR 67249, November 9,
2000) do not apply to this order. In
addition, this order does not impose any
enforceable duty or contain any
unfunded mandate as described under
Title II of the Unfunded Mandates
Reform Act (UMRA) (2 U.S.C. 1531–
1538).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Difenzoquat,
Pesticides and pests, Reporting and
recordkeeping requirements.
E. Executive Orders 13045: Protection of
Children From Environmental Health
Risks and Safety Risks; Executive Order
13211: Actions Concerning Regulations
That Significantly Affect Energy Supply,
Distribution, or Use, and Executive
Order 12898: Federal Actions To
Address Environmental Justice in
Minority Populations and Low Income
Populations
As indicated previously, this action is
not a ‘‘regulatory action’’ as defined by
Executive Order 12866. As a result, this
action is not subject to Executive Order
13045 (62 FR 19885, April 23, 1997) and
Executive Order 13211 (66 FR 28355,
May 22, 2001). In addition, this order
also does not require any special
considerations under Executive Order
12898 (59 FR 7629, February 16, 1994).
F. National Technology Transfer and
Advancement Act
C. Regulatory Flexibility Act
Jkt 229001
75039
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA), (15 U.S.C. 272 note).
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Dated: December 12, 2012.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2012–30617 Filed 12–18–12; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2011–0772; FRL–9369–5]
Propiconazole; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
tolerances for residues of propiconazole
in or on sugarcane, cane. Syngenta Crop
Protection, LLC requested these
tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective
December 19, 2012. Objections and
requests for hearings must be received
on or before February 19, 2013, and
must be filed in accordance with the
instructions provided in 40 CFR part
178 (see also Unit I.C. of the
SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2011–0772, 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.
FOR FURTHER INFORMATION CONTACT: Erin
Malone, Registration Division (7505P),
SUMMARY:
E:\FR\FM\19DER1.SGM
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Agencies
[Federal Register Volume 77, Number 244 (Wednesday, December 19, 2012)]
[Rules and Regulations]
[Pages 75037-75039]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-30617]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2012-0441; FRL-9372-9]
Difenzoquat; Data Call-in Order for Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final order.
-----------------------------------------------------------------------
SUMMARY: This order requires the submission of various data to support
the continuation of the tolerances for the pesticide, difenzoquat.
Pesticide tolerances are established under the Federal Food, Drug, and
Cosmetic Act (FFDCA). Following publication of this order, persons who
are interested in the continuation of the difenzoquat tolerances must
notify the Agency by completing and submitting the required section
408(f) Order Response Form (available in the docket) within 90 days. If
the Agency does not receive within 90 days after publication of the
final order a section 408(f) Response Form identifying a person who
agrees to submit the required data, EPA will revoke the difenzoquat
tolerances.
DATES: This final order is effective December 19, 2012. A section
408(f) Order Response Form must be received on or before March 19,
2013.
ADDRESSES: EPA has established a docket for this action under docket
identification (ID) number EPA-HQ-OPP-2012-0441. All documents in the
docket are listed in the docket index available at https://www.regulations.gov. Although listed in the index, some information is
not publicly available, e.g., Confidential Business Information (CBI)
or other information whose disclosure is restricted by statute. Certain
other material, such as copyrighted material, is not placed on the
Internet and will be publicly available only in hard copy form.
Publicly available docket materials are available in the electronic
docket at https://www.regulations.gov, or, if only available in hard
copy, at the OPP Regulatory Public 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.
Submit your section 408(f) Order Response Form, identified by
docket identification (ID) number EPA-HQ-OPP-2012-0441, by one of the
following methods:
Federal eRulemaking Portal: Follow the on-line
instructions for submitting comments.
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.
FOR FURTHER INFORMATION CONTACT: Christina Scheltema, Pesticide Re-
evaluation Division (7508P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460-0001; telephone number: (703) 308-2201; email
address: scheltema.christina@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. 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 electronic access to other related information?
You may access a frequently updated electronic version of 40 CFR
part 180 through the Government Printing Office's e-CFR site at https://ecfr.gpoaccess.gov/cgi/t/text/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl. To access the harmonized test guidelines referenced in
this document electronically, please go to https://www.epa.gov/ocspp and
select ``Test Methods and Guidelines,'' which is listed under
``Documents related to our mission.''
II. Background
A. What action is the agency taking?
In this document EPA is issuing an order requiring the submission
of various data to support the continuation of the difenzoquat
tolerances at 40 CFR 180.369, under section 408 of FFDCA, 21 U.S.C.
346a. Difenzoquat is not currently registered under the Federal
Insecticide, Fungicide, and Rodenticide Act (FIFRA), 7 U.S.C. 136 et
seq. The last FIFRA registration for difenzoquat was canceled in 2010.
However, 25 FFDCA tolerances remain for residues of difenzoquat on the
following commodities: Barley, cattle, goat, hog, horse, poultry,
sheep, and wheat (40 CFR 180.369). Because there are currently no
domestic registrations for difenzoquat, these tolerances are referred
to as ``import tolerances.'' It is these tolerances that are addressed
by the Data Call-In order.
[[Page 75038]]
B. What is the agency's authority for taking this action?
Under section 408(f) of the FFDCA, EPA is authorized to require, by
order, submission of data ``reasonably required to support the
continuation of a tolerance'' when such data cannot be obtained under
the Data Call-In authority of FIFRA section 3(c)(2)(B), or section 4 of
the Toxic Substances Control Act (``TSCA''), 15 U.S.C. 2603. A FFDCA
section 408 Data Call-In order may only be issued following publication
of notice of the order and a 60-day public comment provision.
A section 408(f) Data Call-In order must contain the following
elements:
1. A requirement that one or more persons submit to EPA a notice
identifying the person(s) who commit to submit the data required in the
order.
2. A description of the required data and the required reports
connected to such data;
3. An explanation of why the required data could not be obtained
under section 3(c)(2)(B) of FIFRA or section 4 of TSCA.
4. The required submission date for the notice identifying one or
more interested persons who commit to submit the required data and the
required submission dates for all the data and reports required in the
order (21 U.S.C. 346a(f)(1)(C)).
EPA may by order modify or revoke the affected tolerances if any
one of the following submissions is not made in a timely manner:
1. A notice identifying the one or more interested persons who
commit to submit the data.
2. The data itself.
3. The reports required under a section 408(f) order are not
submitted by the date specified in the order (21 U.S.C. 346a(f)(2)).
C. What preliminary steps were taken by EPA prior to issuing this final
order?
On July 6, 2012 (77 FR 44181) (FRL-9352-9), EPA issued a proposed
Data Call-In order for the pesticide difenzoquat in connection with
tolerances for that pesticide under section 408 of the Federal Food,
Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 346a. The proposed Data Call-
In order included the following studies:
Neurotoxicity Screening Battery (870.6200).
Immunotoxicity Study (870.7800).
Crop Field Trials (860.1500)--(wheat hay, wheat forage,
and barley hay).
III. Summary of Public Comments Received and Agency Response to
Comments
EPA received no comments in response to the July 6, 2012, Federal
Register notice announcing the Agency's proposed Data Call-In order for
difenzoquat. In addition, the Agency has not received any of the data
identified in the proposed order as needed to support the difenzoquat
tolerances.
IV. Final Data Call-in Order
Because no comments were submitted on the proposal and the data
deficiencies identified in the proposed order remain, EPA is issuing
this final Data Call-In order under FFDCA section 408(f)(1)(C) for
difenzoquat in the same form as the proposed order and for the reasons
set forth in that proposed order. Specifically, this order:
1. Requires notice of intent to submit data. A notice identifying
the person or persons who commit to submit the data and reports in
accordance with Unit IV.2. must be submitted to EPA if any person
wishes to support the difenzoquat tolerances. The notice must be
submitted on a section 408(f) Order Response Form which is available in
the electronic docket, https://www.regulations.gov, under docket ID
number EPA-HQ-OPP-2012-0441.
2. Establishes a deadline for submission of notice identifying data
submitters. The notice described in Unit IV.1., identifying data
submitters, must be submitted to and received by EPA on or before March
19, 2013. Instructions on methods for responding to this order
(referred to in this order as a ``section 408(f) Order Response Form'')
are set out under the ADDRESSES section above.
3. Describes data and reports required to support continuation of
the difenzoquat tolerances, requires submission of those data and
reports, and establishes deadlines for submission. The table in this
Unit describes the data and reports required to be submitted on
difenzoquat under this order and the deadlines for the submission of
each study and report. The required submission date is calculated from
March 19, 2013. Thus, for example, if EPA generally allows 12 months to
complete a study, the required submission date for such a study under
this order would be 15 months from the date of publication of the order
in the Federal Register. Studies, study protocols, and reports should
be submitted to the person listed under FOR FURTHER INFORMATION
CONTACT.
Table--Data and Reports Required To Be Submitted on Difenzoquat
----------------------------------------------------------------------------------------------------------------
Timeframe for
OCSPP harmonized guideline No. Study title protocol report Timeframe for data submission
submission
----------------------------------------------------------------------------------------------------------------
870.6200......................... Neurotoxicity Screening Not Required....... March 19, 2015.
Battery.
870.7800......................... Immunotoxicity Study.... 6 months........... March 19, 2014.
860.1500......................... Crop Field Trials (wheat Not Required....... March 19, 2015.
hay, wheat forage, and
barley hay).
----------------------------------------------------------------------------------------------------------------
EPA provided a description of why the required data could not be
obtained under section 3(c)(2)(B) of FIFRA or section 4 of TSCA in the
proposed order and relies on that description in this final order.
V. Failure to Submit Notice of Intent to Submit Data or Data and
Reports
If, by March 19, 2013 the Agency does not receive a section 408(f)
Order Response Form identifying a person who agrees to submit the
required data, EPA will revoke the difenzoquat tolerances at 40 CFR
180.369. Such revocation is subject to the objection and hearing
procedure in FFDCA section 408(g)(2) but the only material issue in
such a procedure is whether a submission required by the order was made
in a timely fashion.
Additional events that may be the basis for modification or
revocation of difenzoquat tolerances include, but are not limited to
the following:
1. No person submits on the required schedule an acceptable
protocol report when such report is required to be submitted to the
Agency for review.
2. No person submits on the required schedule acceptable data as
required by the final order.
[[Page 75039]]
VI. Statutory and Executive Order Reviews
This action, which requires the submission of data in support of
tolerances in accordance with FFDCA section 408, is in the form of an
order and not a rule (21 U.S.C. 346a(f)(1)(C)). Under the
Administrative Procedures Act (APA), orders are expressly excluded from
the definition of a rule (5 U.S.C. 551(4)). Accordingly, the regulatory
assessment requirements imposed on a rulemaking do not apply to this
action, as explained further in the following discussion.
A. Executive Order 12866: Regulatory Planning and Review and Executive
Order 13563: Improving Regulation and Regulatory Review
Because this order is not a ``regulatory action'' as that term is
defined in Executive Order 12866 (58 FR 51735, October 4, 1993), this
action is not subject to review by the Office of Management and Budget
(OMB) under Executive Orders 12866 and 13563 (76 FR 3821, January 21,
2011).
B. Paperwork Reduction Act
This action does not impose additional burdens that require
approval by OMB under the Paperwork Reduction Act (PRA) (44 U.S.C. 3501
et seq.). The information collection activities associated with the
order requesting data from any party interested in supporting certain
tolerances are already approved by OMB under OMB Control No. 2070-0174,
and are identified by EPA ICR No. 2288.01. Burden is defined at 5 CFR
1320.3(b). Under the PRA, an Agency may not conduct or sponsor, and a
person is not required to respond to a collection of information that
requires OMB approval under PRA, unless it has been approved by OMB and
displays a currently valid OMB control number. The OMB control numbers
for EPA's regulations in title 40 of the CFR, after appearing in the
Federal Register, are listed in 40 CFR part 9, and included on the
related collection instrument, or form, if applicable.
C. Regulatory Flexibility Act
Since this order is not a rule under the APA (5 U.S.C. 551(4)), and
does not require the issuance of a proposed rule, the requirements of
the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et seq.) do not
apply.
D. Unfunded Mandates Reform Act; Executive Order 13132: Federalism; and
Executive Order 13175: Consultation and Coordination With Indian Tribal
Governments
This order requests data from any party interested in supporting
certain tolerances and does not impose obligations on any person or
entity including States or tribes; nor does this action alter the
relationships or distribution of power and responsibilities established
by Congress in the preemption provisions of section 408(n)(4) of FFDCA.
As such, the Agency has determined that this action will not have a
substantial direct effect on States or tribal governments, on the
relationship between the national government and the States or tribal
governments, or on the distribution of power and responsibilities among
the various levels of government or between the Federal Government and
Indian tribes. Thus, the Agency has determined that Executive Order
13132 (64 FR 43255, August 10, 1999) and Executive Order 13175 (65 FR
67249, November 9, 2000) do not apply to this order. In addition, this
order does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
(UMRA) (2 U.S.C. 1531-1538).
E. Executive Orders 13045: Protection of Children From Environmental
Health Risks and Safety Risks; Executive Order 13211: Actions
Concerning Regulations That Significantly Affect Energy Supply,
Distribution, or Use, and Executive Order 12898: Federal Actions To
Address Environmental Justice in Minority Populations and Low Income
Populations
As indicated previously, this action is not a ``regulatory action''
as defined by Executive Order 12866. As a result, this action is not
subject to Executive Order 13045 (62 FR 19885, April 23, 1997) and
Executive Order 13211 (66 FR 28355, May 22, 2001). In addition, this
order also does not require any special considerations under Executive
Order 12898 (59 FR 7629, February 16, 1994).
F. National Technology Transfer and Advancement Act
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA), (15 U.S.C. 272 note).
VII. Congressional Review Act
The Congressional Review Act, 5 U.S.C. 801 et seq. does not apply
because this action is not a rule as that term is defined in 5 U.S.C.
804(3).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Difenzoquat, Pesticides and pests, Reporting
and recordkeeping requirements.
Dated: December 12, 2012.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2012-30617 Filed 12-18-12; 8:45 am]
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