Pesticide Registration Review; Draft Human Health and/or Ecological Risk Assessments for Several Pesticides; Notice of Availability, 6154-6155 [2020-02041]
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6154
Federal Register / Vol. 85, No. 23 / Tuesday, February 4, 2020 / Notices
Dated: January 29, 2020.
Kimberly D. Bose,
Secretary.
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; telephone
number: (703) 305–7106; email address:
biscoe.melanie@epa.gov.
SUPPLEMENTARY INFORMATION:
[FR Doc. 2020–02106 Filed 2–3–20; 8:45 am]
BILLING CODE 6717–01–P
I. General Information
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2017–0720; FRL–10004–40]
Pesticide Registration Review; Draft
Human Health and/or Ecological Risk
Assessments for Several Pesticides;
Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of EPA’s draft human health
and/or ecological risk assessments for
the registration review of carboxin,
famoxadone (ecological assessment
only), fenpropimorph, irgarol,
naphthalene acetic acid (also known as
NAA), propargite, telone (1,3-D),
triallate, and triticonazole.
DATES: Comments must be received on
or before April 6, 2020.
ADDRESSES: Submit your comments, to
the docket identification (ID) number for
the specific pesticide of interest
provided in the Table in Unit IV, 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.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, are available at https://
www.epa.gov/dockets.
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 questions on the
registration review program, contact:
Melanie Biscoe, Pesticide Re-Evaluation
Division (7508P), Office of Pesticide
Programs, Environmental Protection
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:48 Feb 03, 2020
Jkt 250001
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
Chemical Review Manager identified in
the Table in Unit IV.
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 preparing and submitting your
comments, see the commenting tips at
https://www.epa.gov/dockets/
comments.html.
3. Environmental justice. EPA seeks to
achieve environmental justice, the fair
treatment and meaningful involvement
of any group, including minority and/or
low income populations, in the
development, implementation, and
enforcement of environmental laws,
regulations, and policies. To help
address potential environmental justice
issues, the Agency seeks information on
any groups or segments of the
population who, as a result of their
location, cultural practices, or other
factors, may have atypical or
disproportionately high and adverse
human health impacts or environmental
PO 00000
Frm 00014
Fmt 4703
Sfmt 4703
effects from exposure to the pesticides
discussed in this document, compared
to the general population.
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 comprehensive
draft human health and/or ecological
risk assessments for all pesticides listed
in the Table in Unit IV. After reviewing
comments received during the public
comment period, EPA may issue a
revised risk assessment, explain any
changes to the draft risk assessment, and
respond to comments and may request
public input on risk mitigation before
completing a proposed registration
review decision for the pesticides listed
in the Table in Unit IV. 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.
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
human health and/or ecological risk
assessments for the pesticides shown in
the following table and opens a 60-day
public comment period on the risk
assessments.
E:\FR\FM\04FEN1.SGM
04FEN1
Federal Register / Vol. 85, No. 23 / Tuesday, February 4, 2020 / Notices
6155
khammond on DSKJM1Z7X2PROD with NOTICES
TABLE—DRAFT RISK ASSESSMENTS BEING MADE AVAILABLE FOR PUBLIC COMMENT
Registration review case name and
No.
Docket ID No.
Carboxin/Oxycarboxin, Case 0012 ....
Famoxadone, Case 7038 ...................
Fenpropimorph, Case 5112 ...............
Irgarol, Case 5031 ..............................
Naphthalene Acetic Acid and its
Salts, Ester, and Acetamide (NAA),
Case 0379.
Propargite, Case 0243 .......................
Telone (1,3-D), Case 0328 ................
Triallate, Case 2695 ...........................
Triticonazole, Case 7036 ...................
EPA–HQ–OPP–2004–0124
EPA–HQ–OPP–2015–0094
EPA–HQ–OPP–2014–0404
EPA–HQ–OPP–2010–0003
EPA–HQ–OPP–2014–0773
Tiffany Green, green.tiffany@epa.gov, (703) 347–0314.
Christina Scheltema, scheltema.christina@epa.gov, (703) 305–8401.
Peter Bergquist, bergquist.peter@epa.gov, (703) 347–8563.
SanYvette Williams, williams.sanyvette@epa.gov, (703) 305–7702.
Linsey Walsh, walsh.linsey@epa.gov, (703) 347–0588.
EPA–HQ–OPP–2014–0131
EPA–HQ–OPP–2013–0154
EPA–HQ–OPP–2014–0573
EPA–HQ–OPP–2015–0602
Wilhelmena Livingston, livingston.wilhelmena@epa.gov, (703) 308–8025.
Michelle Nolan, nolan.michelle@epa.gov, (703) 347–0258.
Katherine St. Clair, stclair.Katherine@epa.gov, (703) 347–8778.
Christian Bongard, bongard.christian@epa.gov, (703) 347–0337.
Pursuant to 40 CFR 155.53(c), EPA is
providing an opportunity, through this
notice of availability, for interested
parties to provide comments and input
concerning the Agency’s draft human
health and/or ecological risk
assessments for the pesticides listed in
the Table in Unit IV. The Agency will
consider all comments received during
the public comment period and make
changes, as appropriate, to a draft
human health and/or ecological risk
assessment. EPA may then issue a
revised risk assessment, explain any
changes to the draft risk assessment, and
respond to comments.
Information submission requirements.
Anyone may submit data or information
in response to this document. To be
considered during a pesticide’s
registration review, the submitted data
or information must meet the following
requirements:
• To ensure that EPA will consider
data or information submitted,
interested persons must submit the data
or information during the comment
period. The Agency may, at its
discretion, consider data or information
submitted at a later date.
• The data or information submitted
must be presented in a legible and
useable form. For example, an English
translation must accompany any
material that is not in English and a
written transcript must accompany any
information submitted as an
audiographic or videographic record.
Written material may be submitted in
paper or electronic form.
• Submitters must clearly identify the
source of any submitted data or
information.
• Submitters may request the Agency
to reconsider data or information that
the Agency rejected in a previous
review. However, submitters must
explain why they believe the Agency
should reconsider the data or
information in the pesticide’s
registration review.
VerDate Sep<11>2014
17:48 Feb 03, 2020
Jkt 250001
Chemical review manager and
contact information
As provided in 40 CFR 155.58, the
registration review docket for each
pesticide case will remain publicly
accessible through the duration of the
registration review process; that is, until
all actions required in the final decision
on the registration review case have
been completed.
Authority: 7 U.S.C. 136 et seq.
Dated: January 27, 2020.
Mary Reaves,
Acting Director, Pesticide Re-Evaluation
Division, Office of Pesticide Programs.
[FR Doc. 2020–02041 Filed 2–3–20; 8:45 am]
BILLING CODE 6560–50–P
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.html.
Additional instructions on commenting
or visiting the docket, along with more
information about dockets generally, are
available at https://www.epa.gov/
dockets.
For
pesticide specific information, contact:
The Chemical Review Manager for the
pesticide of interest identified in Unit
IV.
For general questions 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:
FOR FURTHER INFORMATION CONTACT:
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2017–0720; FRL–10004–43]
Pesticide Registration Review;
Pesticide Dockets Opened for Review
and Comment; Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of the EPA’s preliminary
work plans for the following chemicals:
Methoprene, pyridalyl, and
spirotetramat. With this document, the
EPA is opening the public comment
period for registration review for these
chemicals.
DATES: Comments must be received on
or before April 6, 2020.
ADDRESSES: Submit your comments, to
the docket identification (ID) number for
the specific pesticide of interest
provided in the Table in Unit IV, 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)
SUMMARY:
PO 00000
Frm 00015
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, 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
Chemical Review Manager identified in
the Table in Unit IV.
E:\FR\FM\04FEN1.SGM
04FEN1
Agencies
[Federal Register Volume 85, Number 23 (Tuesday, February 4, 2020)]
[Notices]
[Pages 6154-6155]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-02041]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2017-0720; FRL-10004-40]
Pesticide Registration Review; Draft Human Health and/or
Ecological Risk Assessments for Several Pesticides; Notice of
Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the availability of EPA's draft human
health and/or ecological risk assessments for the registration review
of carboxin, famoxadone (ecological assessment only), fenpropimorph,
irgarol, naphthalene acetic acid (also known as NAA), propargite,
telone (1,3-D), triallate, and triticonazole.
DATES: Comments must be received on or before April 6, 2020.
ADDRESSES: Submit your comments, to the docket identification (ID)
number for the specific pesticide of interest provided in the Table in
Unit IV, 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.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, are available at https://www.epa.gov/dockets.
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 questions 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 Chemical Review Manager identified in the Table in Unit IV.
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 preparing and submitting
your comments, see the commenting tips at https://www.epa.gov/dockets/comments.html.
3. Environmental justice. EPA seeks to achieve environmental
justice, the fair treatment and meaningful involvement of any group,
including minority and/or low income populations, in the development,
implementation, and enforcement of environmental laws, regulations, and
policies. To help address potential environmental justice issues, the
Agency seeks information on any groups or segments of the population
who, as a result of their location, cultural practices, or other
factors, may have atypical or disproportionately high and adverse human
health impacts or environmental effects from exposure to the pesticides
discussed in this document, compared to the general population.
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 comprehensive draft human health and/or
ecological risk assessments for all pesticides listed in the Table in
Unit IV. After reviewing comments received during the public comment
period, EPA may issue a revised risk assessment, explain any changes to
the draft risk assessment, and respond to comments and may request
public input on risk mitigation before completing a proposed
registration review decision for the pesticides listed in the Table in
Unit IV. 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.
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 human health and/or ecological risk assessments for the
pesticides shown in the following table and opens a 60-day public
comment period on the risk assessments.
[[Page 6155]]
Table--Draft Risk Assessments Being Made Available for Public Comment
----------------------------------------------------------------------------------------------------------------
Chemical review manager and
Registration review case name and No. Docket ID No. contact information
----------------------------------------------------------------------------------------------------------------
Carboxin/Oxycarboxin, Case 0012...... EPA-HQ-OPP-2004-0124 Tiffany Green,
[email protected], (703)
347-0314.
Famoxadone, Case 7038................ EPA-HQ-OPP-2015-0094 Christina Scheltema,
[email protected],
(703) 305-8401.
Fenpropimorph, Case 5112............. EPA-HQ-OPP-2014-0404 Peter Bergquist,
[email protected],
(703) 347-8563.
Irgarol, Case 5031................... EPA-HQ-OPP-2010-0003 SanYvette Williams,
[email protected],
(703) 305-7702.
Naphthalene Acetic Acid and its EPA-HQ-OPP-2014-0773 Linsey Walsh,
Salts, Ester, and Acetamide (NAA), [email protected], (703)
Case 0379. 347-0588.
Propargite, Case 0243................ EPA-HQ-OPP-2014-0131 Wilhelmena Livingston,
[email protected], (703) 308-8025.
Telone (1,3-D), Case 0328............ EPA-HQ-OPP-2013-0154 Michelle Nolan,
[email protected],
(703) 347-0258.
Triallate, Case 2695................. EPA-HQ-OPP-2014-0573 Katherine St. Clair,
[email protected],
(703) 347-8778.
Triticonazole, Case 7036............. EPA-HQ-OPP-2015-0602 Christian Bongard,
[email protected],
(703) 347-0337.
----------------------------------------------------------------------------------------------------------------
Pursuant to 40 CFR 155.53(c), EPA is providing an opportunity,
through this notice of availability, for interested parties to provide
comments and input concerning the Agency's draft human health and/or
ecological risk assessments for the pesticides listed in the Table in
Unit IV. The Agency will consider all comments received during the
public comment period and make changes, as appropriate, to a draft
human health and/or ecological risk assessment. EPA may then issue a
revised risk assessment, explain any changes to the draft risk
assessment, and respond to comments.
Information submission requirements. Anyone may submit data or
information in response to this document. To be considered during a
pesticide's registration review, the submitted data or information must
meet the following requirements:
To ensure that EPA will consider data or information
submitted, interested persons must submit the data or information
during the comment period. The Agency may, at its discretion, consider
data or information submitted at a later date.
The data or information submitted must be presented in a
legible and useable form. For example, an English translation must
accompany any material that is not in English and a written transcript
must accompany any information submitted as an audiographic or
videographic record. Written material may be submitted in paper or
electronic form.
Submitters must clearly identify the source of any
submitted data or information.
Submitters may request the Agency to reconsider data or
information that the Agency rejected in a previous review. However,
submitters must explain why they believe the Agency should reconsider
the data or information in the pesticide's registration review.
As provided in 40 CFR 155.58, the registration review docket for
each pesticide case will remain publicly accessible through the
duration of the registration review process; that is, until all actions
required in the final decision on the registration review case have
been completed.
Authority: 7 U.S.C. 136 et seq.
Dated: January 27, 2020.
Mary Reaves,
Acting Director, Pesticide Re-Evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2020-02041 Filed 2-3-20; 8:45 am]
BILLING CODE 6560-50-P