Pesticide Registration Review; Interim Decisions and Case Closures for Several Pesticides; Notice of Availability, 58656-58658 [2021-23041]
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58656
Federal Register / Vol. 86, No. 202 / Friday, October 22, 2021 / Notices
TABLE 1—PROPOSED INTERIM DECISIONS—Continued
Registration review case name
and No.
lotter on DSK11XQN23PROD with NOTICES1
Tetraconazole, Case Number
7043.
Docket ID No.
EPA–HQ–OPP–2015–0061 .............................
The registration review docket for a
pesticide includes earlier documents
related to the registration review case.
For example, the review opened with a
Preliminary Work Plan, for public
comment. A Final Work Plan was
placed in the docket following public
comment on the Preliminary Work Plan.
The documents in the dockets
describe EPA’s rationales for conducting
additional risk assessments for the
registration review of the pesticides
included in the tables in Unit IV, as well
as the Agency’s subsequent risk findings
and consideration of possible risk
mitigation measures. These proposed
interim registration review decisions are
supported by the rationales included in
those documents. Following public
comment, the Agency will issue interim
or final registration review decisions for
the pesticides listed in Table 1 in Unit
IV.
The registration review final rule at 40
CFR 155.58(a) provides for a minimum
60-day public comment period on all
proposed interim registration review
decisions. This comment period is
intended to provide an opportunity for
public input and a mechanism for
initiating any necessary amendments to
the proposed interim decision. All
comments should be submitted using
the methods in ADDRESSES and must be
received by EPA on or before the closing
date. These comments will become part
of the docket for the pesticides included
in the Tables in Unit IV. Comments
received after the close of the comment
period will be marked ‘‘late.’’ EPA is not
required to consider these late
comments.
The Agency will carefully consider all
comments received by the closing date
and may provide a ‘‘Response to
Comments Memorandum’’ in the
docket. The interim registration review
decision will explain the effect that any
comments had on the interim decision
and provide the Agency’s response to
significant comments.
Background on the registration review
program is provided at: https://
www.epa.gov/pesticide-reevaluation.
17:47 Oct 21, 2021
Veronica Dutch, dutch.veronica@epa.gov, (703) 308–8585.
Dated: October 18, 2021.
Mary Elissa Reaves,
Director, Pesticide Re-Evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2021–23043 Filed 10–21–21; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2017–0751; FRL–9076–01–
OCSPP]
Pesticide Registration Review; Interim
Decisions and Case Closures for
Several Pesticides; Notice of
Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of EPA’s interim registration
review decisions for the following
chemicals: Amicarbazone;
aminopyralid; azadirachtin, cold
pressed neem oil and clarified
hydrophobic neem oil; benzoic acid;
endothall and salts; ethofumesate;
fluoxastrobin; forchlorfenuron; gammacyhalothrin; inorganic halides;
ipconazole; L-lactic acid; lambdacyhalothrin; metam/MITC; metconazole;
myclobutanil; novaluron; picloram;
prometon; prothioconazole; and
pyrasulfotole. In addition, it announces
the closure of the registration review
case for propazine.
FOR FURTHER INFORMATION CONTACT: For
pesticide specific information, contact:
The Chemical Review Manager for the
pesticide of interest identified in the
Table in Unit IV.
For general information on the
registration review program, contact:
Melanie Biscoe, Pesticide Re-evaluation
Division (7508P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; telephone
number: (703) 305–7106; email address:
biscoe.melanie@epa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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
(Authority: 7 U.S.C. 136 et seq.)
VerDate Sep<11>2014
Chemical review manager and contact information
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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
in the Table in Unit IV.
B. How can I get copies of this document
and other related information?
The dockets these cases, identified by
the docket identification (ID) number for
the specific pesticide of interest
provided in the Table in Unit IV., are
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), West William
Jefferson Clinton 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.
Due to the public health concerns
related to COVID–19, the EPA Docket
Center (EPA/DC) and Reading Room is
closed to visitors with limited
exceptions. The staff continues to
provide remote customer service via
email, phone, and webform. For the
latest status information on EPA/DC
services and docket access, visit https://
www.epa.gov/dockets.
II. Background
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, the pesticide can
perform its intended function without
unreasonable adverse effects on human
health or the environment. As part of
the registration review process, the
Agency has completed interim decisions
for all pesticides listed in the Table in
Unit IV. Through this program, EPA is
ensuring that each pesticide’s
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Federal Register / Vol. 86, No. 202 / Friday, October 22, 2021 / Notices
registration is based on current
scientific and other knowledge,
including its effects on human health
and the environment.
III. Authority
EPA is conducting its registration
review of the chemicals listed in the
Table in Unit IV pursuant to section 3(g)
of the Federal Insecticide, Fungicide,
and Rodenticide Act (FIFRA) and the
Procedural Regulations for Registration
Review at 40 CFR part 155, subpart C.
Section 3(g) of FIFRA provides, among
other things, that the registrations of
pesticides are to be reviewed every 15
years. Under FIFRA, a pesticide product
may be registered or remain registered
only if it meets the statutory standard
for registration given in FIFRA section
3(c)(5) (7 U.S.C. 136a(c)(5)). When used
in accordance with widespread and
commonly recognized practice, the
pesticide product must perform its
intended function without unreasonable
adverse effects on the environment; that
is, without any unreasonable risk to
58657
man or the environment, or a human
dietary risk from residues that result
from the use of a pesticide in or on food.
IV. What action is the Agency taking?
Pursuant to 40 CFR 155.58, this notice
announces the availability of EPA’s
interim registration review decisions for
the pesticides shown in the following
table. The interim registration review
decisions are supported by rationales
included in the docket established for
each chemical.
lotter on DSK11XQN23PROD with NOTICES1
TABLE—REGISTRATION REVIEW INTERIM DECISIONS BEING ISSUED
Registration review case name and No.
Docket ID No.
Chemical review manager and contact information
Amicarbazone, Case Number 7262 .................................
EPA–HQ–OPP–2015–0400
Aminopyralid, Case Number 7267 ...................................
EPA–HQ–OPP–2013–0749
Azadirachtin, Cold Pressed Neem Oil, and Clarified Hydrophobic Neem Oil, Case Number 6021.
Benzoic Acid, Case Number 5107 ...................................
EPA–HQ–OPP–2008–0632
Endothall and Salts, Case Number 2245 ........................
Ethofumesate, Case Number 2265 ..................................
EPA–HQ–OPP–2015–0591
EPA–HQ–OPP–2015–0406
Fluoxastrobin, Case Number 7044 ..................................
EPA–HQ–OPP–2015–0295
Forchlorfenuron, Case Number 7057 ..............................
EPA–HQ–OPP–2014–0641
Gamma-cyhalothrin, Case Number 7437 ........................
EPA–HQ–OPP–2010–0479
Inorganic halides, Case Number 4051 ............................
EPA–HQ–OPP–2009–0168
Ipconazole, Case Number 7041 ......................................
EPA–HQ–OPP–2015–0590
L-lactic Acid, Case Number 6062 ....................................
EPA–HQ–OPP–2020–0552
Lambda-cyhalothrin, Case number 7408 .........................
EPA–HQ–OPP–2010–0480
Metam/MITC, Case Number 2390 & 2405 ......................
Metconazole, Case Number 7049 ...................................
EPA–HQ–OPP–2013–0140
& EPA–HQ–OPP–2013–
0242
EPA–HQ–OPP–2015–0013
Samantha Thomas, thomas.samantha@epa.gov, (703)
347–0514.
Rachel Stephenson, stephenson.rachel@epa.gov, (703)
347–8904.
Joseph Mabon, mabon.joseph@epa.gov, (703) 347–
0177.
Megan Snyderman, snyderman.megan@epa.gov, (703)
347–0671.
Robert Little, little.robert@epa.gov, (703) 347–8156.
James Douglass, douglass.james@epa.gov, (703) 347–
8630.
Rachel Fletcher, fletcher.rachel@epa.gov, (703) 347–
0512.
Srijana Shrestha, shrestha.srijana@epa.gov, (703) 305–
6471.
Darius Stanton, stanton.darius@epa.gov, (703) 347–
0433.
Erin Dandridge, dandridge.erin@epa.gov, (703) 347–
0185.
Alex Hazlehurst, hazlehurst.alexander@epa.gov, (703)
347–0221.
SanYvette Williams, williams.sanyvette@epa.gov, (703)
305–7702.
Darius Stanton, stanton.darius@epa.gov, (703) 347–
0433.
Tiffany Green, green.tiffany@epa.gov, (703) 347–0314.
Myclobutanil, Case Number 7006 ....................................
EPA–HQ–OPP–2015–0053
Novaluron Case Number 7615 ........................................
Picloram, Case Number 0096 ..........................................
EPA–HQ–OPP–2015–0171
EPA–HQ–OPP–2013–0740
Prometon, Case Number 2545 ........................................
EPA–HQ–OPP–2013–0068
Prothioconazole, Case Number 7054 ..............................
EPA–HQ–OPP–2015–0474
Pyrasulfotole, Case Number 7272 ...................................
EPA–HQ–OPP–2016–0391
The proposed interim registration
review decisions for the chemicals in
the table above were posted to the
docket and the public was invited to
submit any comments or new
information. EPA addressed the
comments or information received
during the 60-day comment period for
the proposed interim decisions in the
discussion for each pesticide listed in
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17:47 Oct 21, 2021
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EPA–HQ–OPP–2010–0692
Samantha Thomas, thomas.samantha@epa.gov, (703)
347–0514.
Anitha Kisanga, kisanga.anitha@epa.gov, (703) 347–
0540.
Robert Little, little.robert@epa.gov, (703) 347–8156.
Andy Muench, muench.andrew@epa.gov, (703) 347–
8263.
Carolyn Smith, smith.carolyn@epa.gov, (703) 347–
8325.
Rachel Eberius, eberius.rachel@epa.gov, (703) 347–
0492.
James Douglass, douglass.james@epa.gov, (703) 347–
8630.
the table. Comments from the 60-day
comment period that were received may
or may not have affected the Agency’s
interim decision. Pursuant to 40 CFR
155.58(c), the registration review case
docket for the chemicals listed in the
Table will remain open until all actions
required in the interim decision have
been completed.
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This document also announces the
closure of the registration review case
for propazine (Case Number 0230,
Docket ID Number EPA–HQ–OPP–
2013–0250) because the last U.S.
registrations for these pesticides have
been canceled.
Background on the registration review
program is provided at: https://
www.epa.gov/pesticide-reevaluation.
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58658
Federal Register / Vol. 86, No. 202 / Friday, October 22, 2021 / Notices
(Authority: 7 U.S.C. 136 et seq.)
Dated: October 18, 2021.
Mary Elissa Reaves,
Director, Pesticide Re-Evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2021–23041 Filed 10–21–21; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2021–0068; FRL–8732–04–
OCSPP]
Certain New Chemicals; Receipt and
Status Information for September 2021
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
EPA is required under the
Toxic Substances Control Act (TSCA) to
make information publicly available and
to publish information in the Federal
Register pertaining to submissions
under TSCA Section 5, including notice
of receipt of a Premanufacture notice
(PMN), Significant New Use Notice
(SNUN) or Microbial Commercial
Activity Notice (MCAN), including an
amended notice or test information; an
exemption application (Biotech
exemption); an application for a test
marketing exemption (TME), both
pending and/or concluded; a notice of
commencement (NOC) of manufacture
(including import) for new chemical
substances; and a periodic status report
on new chemical substances that are
currently under EPA review or have
recently concluded review. This
document covers the period from 09/01/
2021 to 09/30/2021.
DATES: Comments identified by the
specific case number provided in this
document must be received on or before
November 22, 2021.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2021–0068,
and the specific case number for the
chemical substance related to your
comment, through the Federal
eRulemaking Portal at 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. Additional
instructions on commenting or visiting
the docket, along with more information
about dockets generally, is available at
https://www.epa.gov/dockets.
Due to the public health concerns
related to COVID–19, the EPA Docket
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:47 Oct 21, 2021
Jkt 256001
Center (EPA/DC) and Reading Room is
closed to visitors with limited
exceptions. The staff continues to
provide remote customer service via
email, phone, and webform. For the
latest status information on EPA/DC
services and docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: For
technical information contact: Jim
Rahai, Project Management and
Operations Division (MC 7407M), Office
of Pollution Prevention and Toxics,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; telephone number: (202)
564–8593; email address: rahai.jim@
epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; email address: TSCA-Hotline@
epa.gov.
SUPPLEMENTARY INFORMATION:
I. Executive Summary
A. What action is the Agency taking?
This document provides the receipt
and status reports for the period from
09/01/2021 to 09/30/2021. The Agency
is providing notice of receipt of PMNs,
SNUNs and MCANs (including
amended notices and test information);
an exemption application under 40 CFR
part 725 (Biotech exemption); TMEs,
both pending and/or concluded; NOCs
to manufacture a new chemical
substance; and a periodic status report
on new chemical substances that are
currently under EPA review or have
recently concluded review.
EPA is also providing information on
its website about cases reviewed under
the amended TSCA, including the
section 5 PMN/SNUN/MCAN and
exemption notices received, the date of
receipt, the final EPA determination on
the notice, and the effective date of
EPA’s determination for PMN/SNUN/
MCAN notices on its website at: https://
www.epa.gov/reviewing-new-chemicalsunder-toxic-substances-control-act-tsca/
status-pre-manufacture-notices. This
information is updated on a weekly
basis.
B. What is the Agency’s authority for
taking this action?
Under the Toxic Substances Control
Act (TSCA), 15 U.S.C. 2601 et seq., a
chemical substance may be either an
‘‘existing’’ chemical substance or a
‘‘new’’ chemical substance. Any
chemical substance that is not on EPA’s
TSCA Inventory of Chemical Substances
(TSCA Inventory) is classified as a ‘‘new
chemical substance,’’ while a chemical
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substance that is listed on the TSCA
Inventory is classified as an ‘‘existing
chemical substance.’’ (See TSCA section
3(11).) For more information about the
TSCA Inventory please go to: https://
www.epa.gov/tsca-inventory.
Any person who intends to
manufacture (including import) a new
chemical substance for a non-exempt
commercial purpose, or to manufacture
or process a chemical substance in a
non-exempt manner for a use that EPA
has determined is a significant new use,
is required by TSCA section 5 to
provide EPA with a PMN, MCAN or
SNUN, as appropriate, before initiating
the activity. EPA will review the notice,
make a risk determination on the
chemical substance or significant new
use, and take appropriate action as
described in TSCA section 5(a)(3).
TSCA section 5(h)(1) authorizes EPA
to allow persons, upon application and
under appropriate restrictions, to
manufacture or process a new chemical
substance, or a chemical substance
subject to a significant new use rule
(SNUR) issued under TSCA section
5(a)(2), for ‘‘test marketing’’ purposes,
upon a showing that the manufacture,
processing, distribution in commerce,
use, and disposal of the chemical will
not present an unreasonable risk of
injury to health or the environment.
This is referred to as a test marketing
exemption, or TME. For more
information about the requirements
applicable to a new chemical go to:
https://www.epa.gov/oppt/newchems.
Under TSCA sections 5 and 8 and
EPA regulations, EPA is required to
publish in the Federal Register certain
information, including notice of receipt
of a PMN/SNUN/MCAN (including
amended notices and test information);
an exemption application under 40 CFR
part 725 (biotech exemption); an
application for a TME, both pending
and concluded; NOCs to manufacture a
new chemical substance; and a periodic
status report on the new chemical
substances that are currently under EPA
review or have recently concluded
review.
C. Does this action apply to me?
This action provides information that
is directed to the public in general.
D. Does this action have any
incremental economic impacts or
paperwork burdens?
No.
E. What should I consider as I prepare
my comments for EPA?
1. Submitting confidential business
information (CBI). Do not submit this
information to EPA through
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Agencies
[Federal Register Volume 86, Number 202 (Friday, October 22, 2021)]
[Notices]
[Pages 58656-58658]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-23041]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2017-0751; FRL-9076-01-OCSPP]
Pesticide Registration Review; Interim Decisions and Case
Closures for Several Pesticides; Notice of Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the availability of EPA's interim
registration review decisions for the following chemicals:
Amicarbazone; aminopyralid; azadirachtin, cold pressed neem oil and
clarified hydrophobic neem oil; benzoic acid; endothall and salts;
ethofumesate; fluoxastrobin; forchlorfenuron; gamma-cyhalothrin;
inorganic halides; ipconazole; L-lactic acid; lambda-cyhalothrin;
metam/MITC; metconazole; myclobutanil; novaluron; picloram; prometon;
prothioconazole; and pyrasulfotole. In addition, it announces the
closure of the registration review case for propazine.
FOR FURTHER INFORMATION CONTACT: For pesticide specific information,
contact: The Chemical Review Manager for the pesticide of interest
identified in the Table in Unit IV.
For general information on the registration review program,
contact: Melanie Biscoe, Pesticide Re-evaluation Division (7508P),
Office of Pesticide Programs, Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC 20460-0001; telephone number:
(703) 305-7106; email address: [email protected].
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 in the Table in
Unit IV.
B. How can I get copies of this document and other related information?
The dockets these cases, identified by the docket identification
(ID) number for the specific pesticide of interest provided in the
Table in Unit IV., are 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), West
William Jefferson Clinton 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.
Due to the public health concerns related to COVID-19, the EPA
Docket Center (EPA/DC) and Reading Room is closed to visitors with
limited exceptions. The staff continues to provide remote customer
service via email, phone, and webform. For the latest status
information on EPA/DC services and docket access, visit https://www.epa.gov/dockets.
II. Background
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, the pesticide can perform
its intended function without unreasonable adverse effects on human
health or the environment. As part of the registration review process,
the Agency has completed interim decisions for all pesticides listed in
the Table in Unit IV. Through this program, EPA is ensuring that each
pesticide's
[[Page 58657]]
registration is based on current scientific and other knowledge,
including its effects on human health and the environment.
III. Authority
EPA is conducting its registration review of the chemicals listed
in the Table in Unit IV pursuant to section 3(g) of the Federal
Insecticide, Fungicide, and Rodenticide Act (FIFRA) and the Procedural
Regulations for Registration Review at 40 CFR part 155, subpart C.
Section 3(g) of FIFRA provides, among other things, that the
registrations of pesticides are to be reviewed every 15 years. Under
FIFRA, a pesticide product may be registered or remain registered only
if it meets the statutory standard for registration given in FIFRA
section 3(c)(5) (7 U.S.C. 136a(c)(5)). When used in accordance with
widespread and commonly recognized practice, the pesticide product must
perform its intended function without unreasonable adverse effects on
the environment; that is, without any unreasonable risk to man or the
environment, or a human dietary risk from residues that result from the
use of a pesticide in or on food.
IV. What action is the Agency taking?
Pursuant to 40 CFR 155.58, this notice announces the availability
of EPA's interim registration review decisions for the pesticides shown
in the following table. The interim registration review decisions are
supported by rationales included in the docket established for each
chemical.
Table--Registration Review Interim Decisions Being Issued
----------------------------------------------------------------------------------------------------------------
Chemical review manager
Registration review case name and No. Docket ID No. and contact information
----------------------------------------------------------------------------------------------------------------
Amicarbazone, Case Number 7262......... EPA-HQ-OPP-2015-0400 Samantha Thomas,
[email protected],
(703) 347-0514.
Aminopyralid, Case Number 7267......... EPA-HQ-OPP-2013-0749 Rachel Stephenson,
[email protected], (703) 347-8904.
Azadirachtin, Cold Pressed Neem Oil, EPA-HQ-OPP-2008-0632 Joseph Mabon,
and Clarified Hydrophobic Neem Oil, [email protected],
Case Number 6021. (703) 347-0177.
Benzoic Acid, Case Number 5107......... EPA-HQ-OPP-2010-0692 Megan Snyderman,
[email protected],
(703) 347-0671.
Endothall and Salts, Case Number 2245.. EPA-HQ-OPP-2015-0591 Robert Little,
[email protected],
(703) 347-8156.
Ethofumesate, Case Number 2265......... EPA-HQ-OPP-2015-0406 James Douglass,
[email protected],
(703) 347-8630.
Fluoxastrobin, Case Number 7044........ EPA-HQ-OPP-2015-0295 Rachel Fletcher,
[email protected],
(703) 347-0512.
Forchlorfenuron, Case Number 7057...... EPA-HQ-OPP-2014-0641 Srijana Shrestha,
[email protected]
, (703) 305-6471.
Gamma-cyhalothrin, Case Number 7437.... EPA-HQ-OPP-2010-0479 Darius Stanton,
[email protected],
(703) 347-0433.
Inorganic halides, Case Number 4051.... EPA-HQ-OPP-2009-0168 Erin Dandridge,
[email protected],
(703) 347-0185.
Ipconazole, Case Number 7041........... EPA-HQ-OPP-2015-0590 Alex Hazlehurst,
[email protected], (703) 347-0221.
L-lactic Acid, Case Number 6062........ EPA-HQ-OPP-2020-0552 SanYvette Williams,
[email protected], (703) 305-7702.
Lambda-cyhalothrin, Case number 7408... EPA-HQ-OPP-2010-0480 Darius Stanton,
[email protected],
(703) 347-0433.
Metam/MITC, Case Number 2390 & 2405.... EPA-HQ-OPP-2013-0140 & EPA-HQ-OPP-2013-0242 Tiffany Green,
[email protected],
(703) 347-0314.
Metconazole, Case Number 7049.......... EPA-HQ-OPP-2015-0013 Samantha Thomas,
[email protected],
(703) 347-0514.
Myclobutanil, Case Number 7006......... EPA-HQ-OPP-2015-0053 Anitha Kisanga,
[email protected],
(703) 347-0540.
Novaluron Case Number 7615............. EPA-HQ-OPP-2015-0171 Robert Little,
[email protected],
(703) 347-8156.
Picloram, Case Number 0096............. EPA-HQ-OPP-2013-0740 Andy Muench,
[email protected],
(703) 347-8263.
Prometon, Case Number 2545............. EPA-HQ-OPP-2013-0068 Carolyn Smith,
[email protected],
(703) 347-8325.
Prothioconazole, Case Number 7054...... EPA-HQ-OPP-2015-0474 Rachel Eberius,
[email protected],
(703) 347-0492.
Pyrasulfotole, Case Number 7272........ EPA-HQ-OPP-2016-0391 James Douglass,
[email protected],
(703) 347-8630.
----------------------------------------------------------------------------------------------------------------
The proposed interim registration review decisions for the
chemicals in the table above were posted to the docket and the public
was invited to submit any comments or new information. EPA addressed
the comments or information received during the 60-day comment period
for the proposed interim decisions in the discussion for each pesticide
listed in the table. Comments from the 60-day comment period that were
received may or may not have affected the Agency's interim decision.
Pursuant to 40 CFR 155.58(c), the registration review case docket for
the chemicals listed in the Table will remain open until all actions
required in the interim decision have been completed.
This document also announces the closure of the registration review
case for propazine (Case Number 0230, Docket ID Number EPA-HQ-OPP-2013-
0250) because the last U.S. registrations for these pesticides have
been canceled.
Background on the registration review program is provided at:
https://www.epa.gov/pesticide-reevaluation.
[[Page 58658]]
(Authority: 7 U.S.C. 136 et seq.)
Dated: October 18, 2021.
Mary Elissa Reaves,
Director, Pesticide Re-Evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2021-23041 Filed 10-21-21; 8:45 am]
BILLING CODE 6560-50-P