Pesticide Registration Review; Draft Human Health and/or Ecological Risk Assessments for Several Pesticides; Notice of Availability, 6171-6173 [2022-02198]
Download as PDF
khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 87, No. 23 / Thursday, February 3, 2022 / Notices
can be viewed online at
www.regulations.gov or in person at the
EPA Docket Center, WJC West, Room
3334, 1301 Constitution Ave. NW,
Washington, DC. The telephone number
for the Docket Center is 202–566–1744.
For additional information about EPA’s
public docket, visit https://www.epa.gov/
dockets.
Abstract: This Information Collection
Request (ICR) renews the National
Pollutant Discharge Elimination System
(NPDES) Program ICR and consolidates
the information collection burden and
costs associated with activities
previously reported in 18 of the NPDES
program or NPDES-related ICRs. It
calculates the information collection
burden and costs associated with the
NPDES program, identifies the types of
activities regulated under the NPDES
program, describes the roles and
responsibilities of state governments
and the Agency, and presents the
program areas that address the various
types of regulated activities. This
renewal documents the addition of the
burden and costs for the four existing
NPDES ICRs listed below. Once this
renewal ICR is approved, the following
ICRs will be discontinued: Public
Notification Requirements for Combined
Sewer Overflows (CSOs) in the Great
Lakes Basin (OMB control no. 2040–
0293, EPA ICR 2562.03, expiration date
04/30/24); Effluent Limitation
Guidelines and Standards for the Dental
Category (OMB control no. 2040–0287,
EPA ICR no. 2514.03, expiration 11/30/
23); 2020 NPDES Multi-Sector General
Permit (MSGP) for Industrial
Stormwater Discharges (OMB control
no. 2040–0300, EPA ICR no. 2612.02,
expiration 03/31/24); and NPDES
Electronic Reporting Rule—Phase 2
Extension (OMB Control No.: 2020–
0037, EPA ICR No. 2617.02, expiration
12/31/2023).
The Clean Water Act (CWA) provides
that NPDES permits are required for the
discharge of pollutants to waters of the
United States. The CWA requires EPA to
develop and implement the NPDES
permit program. CWA section 402(b)
allows states to acquire authority to
administer the NPDES program,
enabling them to issue NPDES permits
for discharges within the state. At
present, 47 states and the U.S. Virgin
Islands are authorized to administer the
NPDES permit program. In states that do
not have authority for these programs,
the Agency administers the program and
issues NPDES permits. Because some
permit applications are processed by
states and some by EPA, this ICR
calculates government burden and cost
for both authorized states and EPA. See
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Appendix F.1 for a copy of the
authorizing regulation.
Form Numbers: EPA Form 3510–1;
EPA Form 3510–2A; EPA Form 3510–
2B; EPA Form 3510–2C; EPA Form
3510–2D; EPA Form 3510–2E; EPA
Form 3510–2F; EPA Form 3510–2S.
Respondents/affected entities: Any
point source discharger of pollutants,
publicly owned and privately owned
treatment works (POTWs and PrOTWs),
industrial dischargers to POTWs and
PrOTWs, industrial and commercial
dischargers to water of the United
States, sewage sludge management and
disposal operations, large vessels,
dischargers of stormwater, construction
sites, municipalities, pesticide
applicators, local and state
governments.
Respondent’s obligation to respond:
Mandatory, sections 301, 302, 304, 306,
307, 308, 316(b), 401, 402, 403, 405, and
510 of the CWA; the 1987 Water Quality
Act (WQA) revisions to CWA section
402(p); 40 CFR parts 122, 123, 124, and
125 (and parts 501 and 503 for
Biosolids); and the Great Lakes Critical
Programs Act (CPA).
Estimated number of respondents:
827,180 (total). (Includes 637 States/
Tribes/Territories).
Frequency of response: Varies
depending on the specific response
activity and can range from ongoing and
monthly to once every five years.
Total estimated burden: 31,143,503
hours (per year). Burden is defined at 5
CFR 1320.03(b).
Total estimated cost: $1,732,287,018
(per year), includes $22,999,181
annualized capital or operation &
maintenance costs.
Changes in the estimates: The
majority of the burden hour increase
occurred as a result of an increase in
EPA’s estimates of permittee
respondents, which is largely attributed
to improvements in the NPDES
Integrated Compliance Information
System (ICIS–NPDES) database,
implementation of the Electronic
Reporting Rule Phase 1, and refined
estimates. This ICR eliminates the initial
permit application and compliance
activities for existing Cooling Water
Intake Structure (CWIS) facilities, as
these actions have been completed by
all existing CWIS facilities. The
compliance and administration of small
vessels general permit (sVGP) has been
removed, which lowered the number of
vessel respondents significantly.
Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2022–02169 Filed 2–2–22; 8:45 am]
BILLING CODE 6560–50–P
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6171
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2017–0720; FRL–9450–01–
OCSPP]
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 1,3Propanediamine, N-(3-aminopropyl)-Ndodecyl- (1,3–PAD).
DATES: Comments must be received on
or before April 4, 2022.
ADDRESSES: Submit your comments, to
the docket identification (ID) number for
the specific pesticide of interest
provided in the Table in Unit IV., using
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, are available at
https://www.epa.gov/dockets.
Due to the public health concerns
related to COVID–19, the EPA Docket
Center (EPA/DC) and Reading Room is
open to visitors by appointment only.
For the latest status information on
EPA/DC services and access, visit
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
Table 1 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:
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
wide range of stakeholders including
environmental, human health, farm
worker, and agricultural advocates; the
E:\FR\FM\03FEN1.SGM
03FEN1
6172
Federal Register / Vol. 87, No. 23 / Thursday, February 3, 2022 / Notices
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
Table 1 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/
commenting-epa-dockets.
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 Table 1 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 Table 1 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 Table
1 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
Table 1 and opens a 60-day public
comment period on the risk
assessments.
TABLE 1—DRAFT RISK ASSESSMENTS BEING MADE AVAILABLE FOR PUBLIC COMMENT
Registration review case name and No.
Docket ID No.
khammond on DSKJM1Z7X2PROD with NOTICES
1,3-Propanediamine, N-(3-aminopropyl)-N-dodecyl(1,3 PAD) Case 5109.
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
Table 1 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
VerDate Sep<11>2014
18:08 Feb 02, 2022
Jkt 256001
Chemical review manager and contact information
EPA–HQ–OPP–2014–0406 .......
Megan Snyderman, snyderman.megan@epa.gov,
(202) 566–0639.
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 video-graphic record. Written
PO 00000
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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
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Federal Register / Vol. 87, No. 23 / Thursday, February 3, 2022 / Notices
on the registration review case have
been completed.
Authority: 7 U.S.C. 136 et seq.
Dated: January 27, 2022.
Mary Reaves,
Director, Pesticide Re-Evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2022–02198 Filed 2–2–22; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9535–01–OA]
Notification of Public Meeting
Environmental Protection
Agency (EPA).
ACTION: Notification of public meeting.
AGENCY:
Pursuant to the Federal
Advisory Committee Act (FACA), EPA
hereby provides notice of a meeting of
the Local Government Advisory
Committee (LGAC) and the Small
Communities Advisory Subcommittee
(SCAS) on the date and times described
below. This meeting will be open to the
public. For information on public
attendance and participation, please see
the registration information under
SUPPLEMENTARY INFORMATION section.
DATES: The SCAS will meet virtually
February 17th, 2022, starting at 11:30
a.m. through 1:00 p.m. Eastern Time.
The LGAC will meet virtually February
17th, 2022, starting at 2:00 p.m. through
4:30 p.m. Eastern Time.
FOR FURTHER INFORMATION CONTACT:
Paige Lieberman, Designated Federal
Officer (DFO), at LGAC@epa.gov or 202–
564–9957.
Information on Accessibility: For
information on access or services for
individuals requiring accessibility
accommodations, please contact Paige
Lieberman by email at LGAC@epa.gov.
To request accommodation, please do so
five (5) business days prior to the
meeting, to give EPA as much time as
possible to process your request.
SUPPLEMENTARY INFORMATION:
SUMMARY:
khammond on DSKJM1Z7X2PROD with NOTICES
I. General Information
Following the passage of the historic
Bipartisan Infrastructure Law (BIL), the
U.S. Environmental Protection Agency
(EPA) will be making significant
investments in the health, equity, and
resilience of American communities.
With unprecedented funding to support
our national infrastructure, EPA will
improve people’s health and safety, help
create good-paying jobs, and increase
climate resilience throughout the
country.
VerDate Sep<11>2014
18:08 Feb 02, 2022
Jkt 256001
As EPA works to implement the law,
EPA has asked the LGAC for their input
on the following:
• How can we ensure that
investments in water infrastructure
promote sustainable and healthy
communities?
• Are there specific recommendations
for how EPA can prioritize equity,
environmental justice, and the lived
experience of those most impacted by
water pollution?
• Are there technical resources or
assistance that EPA can provide to help
local governments upgrade their water
and wastewater infrastructure?
• How can EPA make funding more
accessible to local governments and
more adaptable to the unique needs a
community faces—particularly
underserved communities?
• Are there specific recommendations
for how EPA can include workforce
development as part of the
implementation of this bill?
• Do you have specific
recommendations for how EPA can
encourage consideration of climate
impacts (e.g., GHG mitigation,
adaptation, resilience) in the projects
funded?
• Is there specific technical assistance
that EPA should offer local governments
to ensure they plan for, develop and
build infrastructure that supports
multiple community goals, including
improving environmental and economic
outcomes, supporting equity and
environmental justice, and increasing
communities’ abilities to create climate
resilience?
• Is there specific input you have for
EPA as it develops the Clean School Bus
program the in BIL?
During this meeting the LGAC will
present, finalize and formally adopt
final recommendations for charge
questions noted above.
Prior to the LGAC meeting, the SCAS
will convene to discuss and provide
input from their perspective on the
LGAC’s draft recommendations for
implementation of the Bipartisan
Infrastructure Law (BIL).
All interested persons are invited to
attend and participate. The SCAS will
hear comments from the public from
12:45–1:00 p.m. (EST). The LGAC will
hear comments from the public from
3:15–3:30 p.m. (EST). Individuals or
organizations wishing to address the
Committee or Subcommittee will be
allowed a maximum of five (5) minutes
to present their point of view. Also,
written comments should be submitted
electronically to LGAC@epa.gov for the
LGAC and SCAS. Please contact the
DFO at the email listed under FOR
FURTHER INFORMATION CONTACT to
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6173
schedule a time on the agenda by
February 14, 2022. Time will be allotted
on a first-come first-served basis, and
the total period for comments may be
extended if the number of requests for
appearances requires it.
Registration: The meeting will be held
virtually through an online audio and
video platform. Members of the public
who wish to participate should register
by contacting the Designated Federal
Officer (DFO) at LGAC@epa.gov by
February 11, 2022. The agenda and
other supportive meeting materials will
be available online at https://
www.epa.gov/ocir/local-governmentadvisory-committee-lgac and can be
obtained by written request to the DFO.
In the event of cancellation for
unforeseen circumstances, please
contact the DFO or check the website
above for reschedule information.
Julian Bowles,
Director, State and Local Relations, Office
of Congressional and Intergovernmental
Relations.
[FR Doc. 2022–02300 Filed 2–2–22; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL MARITIME COMMISSION
[Docket No. 20–10; Petition No. P1–20]
Investigation Into Conditions Created
by Canadian Ballast Water Regulations
in the U.S./Canada Great Lakes Trade
Federal Maritime Commission.
Request for comments.
AGENCY:
ACTION:
Because of developments
within Canada and the United States,
the Federal Maritime Commission
(Commission) is seeking additional
public comments on a petition filed by
the Lake Carriers’ Association
(Petitioner) alleging that conditions
created by the Government of Canada
(Canada) are unfavorable to shipping in
the United States/Canada trade.
DATES: Submit comments on or before
March 7, 2022.
ADDRESSES: You may submit comments,
identified by Docket No. 20–10, by the
following method:
• Email: secretary@fmc.gov. For
comments, include in the subject line:
‘‘Docket No. 20–10, Comments on
Conditions Created by Canadian Ballast
Water Regulations in the U.S./Canada
Great Lakes Trade.’’ Comments should
be attached to the email as a Microsoft
Word or text searchable PDF document.
Docket: For access to the docket to
read background documents or public
comments received, go to the
Commission’s Electronic Reading Room
SUMMARY:
E:\FR\FM\03FEN1.SGM
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Agencies
[Federal Register Volume 87, Number 23 (Thursday, February 3, 2022)]
[Notices]
[Pages 6171-6173]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-02198]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2017-0720; FRL-9450-01-OCSPP]
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 1,3-Propanediamine, N-(3-aminopropyl)-N-dodecyl- (1,3-PAD).
DATES: Comments must be received on or before April 4, 2022.
ADDRESSES: Submit your comments, to the docket identification (ID)
number for the specific pesticide of interest provided in the Table in
Unit IV., using 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, are available at https://www.epa.gov/dockets.
Due to the public health concerns related to COVID-19, the EPA
Docket Center (EPA/DC) and Reading Room is open to visitors by
appointment only. For the latest status information on EPA/DC services
and access, visit 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 Table 1 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
[[Page 6172]]
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
Table 1 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/commenting-epa-dockets.
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 Table 1 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 Table 1 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 Table 1 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 Table 1 and opens a 60-day public comment period on
the risk assessments.
Table 1--Draft Risk Assessments Being Made Available for Public Comment
------------------------------------------------------------------------
Chemical review
Registration review case name manager and
and No. Docket ID No. contact
information
------------------------------------------------------------------------
1,3-Propanediamine, N-(3- EPA-HQ-OPP-2014-04 Megan Snyderman,
aminopropyl)-N-dodecyl- (1,3 06. [email protected]
PAD) Case 5109. pa.gov, (202) 566-
0639.
------------------------------------------------------------------------
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 Table 1 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 audio-graphic or video-
graphic 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
[[Page 6173]]
on the registration review case have been completed.
Authority: 7 U.S.C. 136 et seq.
Dated: January 27, 2022.
Mary Reaves,
Director, Pesticide Re-Evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2022-02198 Filed 2-2-22; 8:45 am]
BILLING CODE 6560-50-P