Certain New Chemicals or Significant New Uses; Statements of Findings for May, June, and July 2022, 51412-51413 [2022-18011]
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51412
Federal Register / Vol. 87, No. 161 / Monday, August 22, 2022 / Notices
o. Final amendments to the
application must be filed with the
Commission no later than 30 days from
the issuance date of the notice of ready
for environmental analysis.
Dated: August 16, 2022.
Kimberly D. Bose,
Secretary.
[FR Doc. 2022–18067 Filed 8–19–22; 8:45 am]
BILLING CODE 6717–01–P
and Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; telephone
number: (202) 564–1667; email address:
edelstein.rebecca@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:
ENVIRONMENTAL PROTECTION
AGENCY
I. Executive Summary
[EPA–HQ–OPPT–2022–0116; FRL–9412–16–
OCSPP]
Certain New Chemicals or Significant
New Uses; Statements of Findings for
May, June, and July 2022
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The Toxic Substances Control
Act (TSCA) requires EPA to publish in
the Federal Register a statement of its
findings after its review of certain TSCA
submissions when EPA makes a finding
that a new chemical substance or
significant new use is not likely to
present an unreasonable risk of injury to
health or the environment. Such
statements apply to premanufacture
notices (PMNs), microbial commercial
activity notices (MCANs), and
significant new use notices (SNUNs)
submitted to EPA under TSCA. This
document presents statements of
findings made by EPA on such
submissions during the period from
May 1, 2022 to July 31, 2022.
ADDRESSES: The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPPT–2022–0116, is
available online at https://
www.regulations.gov or in-person at the
Office of Pollution Prevention and
Toxics Docket (OPPT Docket),
Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC.
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 OPPT
Docket is (202) 566–0280. 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: Rebecca
Edelstein, New Chemical Division
(7405M), Office of Pollution Prevention
jspears on DSK121TN23PROD with NOTICES
SUMMARY:
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A. Does this action apply to me?
This action provides information that
is directed to the public in general.
B. What action is the Agency taking?
This document lists the statements of
findings made by EPA after review of
submissions under TSCA section 5(a)
that certain new chemical substances or
significant new uses are not likely to
present an unreasonable risk of injury to
health or the environment. This
document presents statements of
findings made by EPA during the
reporting period.
C. What is the Agency’s authority for
taking this action?
TSCA section 5(a)(3) requires EPA to
review a submission under TSCA
section 5(a) and make one of the
following specific findings:
• The chemical substance or
significant new use presents an
unreasonable risk of injury to health or
the environment;
• The information available to EPA is
insufficient to permit a reasoned
evaluation of the health and
environmental effects of the chemical
substance or significant new use;
• The information available to EPA is
insufficient to permit a reasoned
evaluation of the health and
environmental effects and the chemical
substance or significant new use may
present an unreasonable risk of injury to
health or the environment;
• The chemical substance is or will
be produced in substantial quantities,
and such substance either enters or may
reasonably be anticipated to enter the
environment in substantial quantities or
there is or may be significant or
substantial human exposure to the
substance; or
• The chemical substance or
significant new use is not likely to
present an unreasonable risk of injury to
health or the environment.
Under TSCA, the unreasonable risk
findings must be made without
consideration of costs or other non-risk
factors, including an unreasonable risk
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to a potentially exposed or susceptible
subpopulation identified as relevant
under the conditions of use. The term
‘‘conditions of use’’ is defined in TSCA
section 3 to mean ‘‘the circumstances, as
determined by the Administrator, under
which a chemical substance is intended,
known, or reasonably foreseen to be
manufactured, processed, distributed in
commerce, used, or disposed of.’’
TSCA section 5(g) requires EPA to
publish in the Federal Register a
statement of its findings after its review
of a submission under TSCA section
5(a) when EPA makes a finding that a
new chemical substance or significant
new use is not likely to present an
unreasonable risk of injury to health or
the environment. Such statements apply
to PMNs, MCANs, and SNUNs
submitted to EPA under TSCA section
5.
Anyone who plans to manufacture
(which includes import) a new chemical
substance for a non-exempt commercial
purpose and any manufacturer or
processor wishing to engage in a use of
a chemical substance designated by EPA
as a significant new use must submit a
notice to EPA at least 90 days before
commencing manufacture of the new
chemical substance or before engaging
in the significant new use.
The submitter of a notice to EPA for
which EPA has made a finding of ‘‘not
likely to present an unreasonable risk of
injury to health or the environment’’
may commence manufacture of the
chemical substance or manufacture or
processing for the significant new use
notwithstanding any remaining portion
of the applicable review period.
II. Statements of Findings Under TSCA
Section 5(a)(3)(C)
In this unit, EPA provides the
following information (to the extent that
such information is not claimed as
Confidential Business Information
(CBI)) on the PMNs, MCANs and
SNUNs for which, during this period,
EPA has made findings under TSCA
section 5(a)(3)(C) that the new chemical
substances or significant new uses are
not likely to present an unreasonable
risk of injury to health or the
environment:
The following list provides the EPA
case number assigned to the TSCA
section 5(a) submission and the
chemical identity (generic name if the
specific name is claimed as CBI).
• J–22–0012, J–22–0013, Genetically
modified microorganism for the
production of a chemical substance
(Generic Name).
To access EPA’s decision document
describing the basis of the ‘‘not likely to
present an unreasonable risk’’ finding
E:\FR\FM\22AUN1.SGM
22AUN1
Federal Register / Vol. 87, No. 161 / Monday, August 22, 2022 / Notices
made by EPA under TSCA section
5(a)(3)(C), look up the specific case
number at https://www.epa.gov/
reviewing-new-chemicals-under-toxicsubstances-control-act-tsca/chemicalsdetermined-not-likely.
Authority: 15 U.S.C. 2601 et seq.
Dated: August 15, 2022.
Madison Le,
Director, New Chemicals Division, Office of
Pollution Prevention and Toxics.
telephone number: (202) 566–1030;
email address: RDFRNotices@epa.gov.
The mailing address for each contact
person: Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001. As part of the mailing
address, include the contact person’s
name, division, and mail code.
SUPPLEMENTARY INFORMATION:
I. General Information
[FR Doc. 2022–18011 Filed 8–19–22; 8:45 am]
A. Does this action apply to me?
BILLING CODE 6560–50–P
This action provides information that
is directed to the public in general.
ENVIRONMENTAL PROTECTION
AGENCY
B. What should I consider as I prepare
my comments for EPA?
jspears on DSK121TN23PROD with NOTICES
[EPA–HQ–OPP–2022–0160; FRL–9409–04–
OCSPP]
1. Submitting CBI. Do not submit CBI
information to EPA through https://
www.regulations.gov/ or email. Clearly
Pesticide Product Registration;
mark the part or all of the information
Receipt of Applications for New Active
that you claim to be CBI. For CBI
Ingredients—July 2022
information in a disk or CD–ROM that
you mail to EPA, mark the outside of the
AGENCY: Environmental Protection
disk or CD–ROM as CBI and then
Agency (EPA).
identify electronically within the disk or
ACTION: Notice.
CD–ROM the specific information that
SUMMARY: EPA has received applications is claimed as CBI. In addition to one
to register pesticide products containing complete version of the comment that
includes information claimed as CBI, a
active ingredients not included in any
copy of the comment that does not
currently registered pesticide products.
contain the information claimed as CBI
Pursuant to the Federal Insecticide,
must be submitted for inclusion in the
Fungicide, and Rodenticide Act
(FIFRA), EPA is hereby providing notice public docket. Information so marked
will not be disclosed except in
of receipt and opportunity to comment
accordance with procedures set forth in
on these applications.
40 CFR part 2.
DATES: Comments must be received on
2. Tips for preparing your comments.
or before September 21, 2022.
When preparing and submitting your
ADDRESSES: Submit your comments,
comments, see the commenting tips at
identified by the docket identification
https://www.epa.gov/dockets/epa(ID) number and the EPA File Symbol or
dockets.
the EPA Registration Number of interest
3. Environmental justice. EPA seeks to
as shown in the body of this document,
achieve environmental justice, the fair
through the Federal eRulemaking Portal
treatment and meaningful involvement
at https://www.regulations.gov. Follow
of any group, including minority and/or
the online instructions for submitting
low-income populations, in the
comments. Do not submit electronically
development, implementation, and
any information you consider to be
enforcement of environmental laws,
Confidential Business Information (CBI)
regulations, and policies. To help
or other information whose disclosure is
address potential environmental justice
restricted by statute. For the latest status
issues, the Agency seeks information on
information on EPA/DC services and
any groups or segments of the
access, visit https://www.epa.gov/
population who, as a result of their
dockets.
location, cultural practices, or other
FOR FURTHER INFORMATION CONTACT:
factors, may have atypical or
Each application summary in Unit II
disproportionately high and adverse
specifies a contact division. The
human health impacts or environmental
appropriate division contacts are
effects from exposure to the pesticides
identified as follows:
discussed in this document, compared
• BPPD (Biopesticides and Pollution
to the general population.
Prevention Division) (Mail Code
7511M); Charles Smith; main telephone II. Registration Applications
EPA has received applications to
number: (202) 566–1400; email address:
register pesticide products containing
BPPDFRNotices@epa.gov.
active ingredients not included in any
• RD (Registration Division) (Mail
Code 7505T); Marietta Echeverria; main currently registered pesticide products.
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51413
Pursuant to the provisions of FIFRA
section 3(c)(4) (7 U.S.C. 136a(c)(4)), and
40 CFR 152.102, EPA is hereby
providing notice of receipt and
opportunity to comment on these
applications. Notice of receipt of these
applications does not imply a decision
by the Agency on these applications.
For actions being evaluated under EPA’s
public participation process for
registration actions, there will be an
additional opportunity for public
comment on the proposed decisions.
Please see EPA’s public participation
website for additional information on
this process (https://www.epa.gov/
pesticide-registration/publicparticipation-process-registrationactions).
New Active Ingredients
File Symbols: 11603–AG, 66222–EOI,
and 66222–EOT. Docket ID number:
EPA–HQ–OPP–2022–0575. Applicant:
ADAMA AGAN c/o Makhteshim Agan
of North America, Inc. (d/b/a ADAMA),
3120 Highwoods Blvd., Suite 100
Raleigh, NC 27604. Product name:
Metamitron Technical, ADA 46701 SC,
and ADA 46343 SG. Active ingredient:
herbicide—metamitron at 98.66%,
14.41%, and 15%, respectively.
Proposed use: Pome Fruit (Crop Group
11–10). Contact: RD.
File Symbol: 52991–UU. Docket ID
number: EPA–HQ–OPP–2022–0659.
Applicant: Bedoukian Research, Inc., 6
Commerce Drive, Danbury, CT 06810.
Product name: Bedoukian Tuta
Absoluta Technical Pheromone. Active
ingredients: Insecticide—(e,z,z)-3,8,11Tetradecatrienyl acetate at 76.50% and
(e,z)-3,8-Tetradecadienyl acetate at
9.30%. Proposed use: For use to
manufacture end-use products intended
to control the tomato leaf miner (Tuta
absoluta). Contact: BPPD.
Dated: August 10, 2022.
Brian Bordelon,
Acting Director, Information Technology and
Resources Management Division, Office of
Program Support.
[FR Doc. 2022–18021 Filed 8–19–22; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–10131–01–R9]
Revision of Approved State Primacy
Program for the State of Hawaii
Environmental Protection
Agency (EPA).
ACTION: Notice of approval.
AGENCY:
Notice is hereby given that
the State of Hawaii revised its approved
SUMMARY:
E:\FR\FM\22AUN1.SGM
22AUN1
Agencies
[Federal Register Volume 87, Number 161 (Monday, August 22, 2022)]
[Notices]
[Pages 51412-51413]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-18011]
=======================================================================
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2022-0116; FRL-9412-16-OCSPP]
Certain New Chemicals or Significant New Uses; Statements of
Findings for May, June, and July 2022
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Toxic Substances Control Act (TSCA) requires EPA to
publish in the Federal Register a statement of its findings after its
review of certain TSCA submissions when EPA makes a finding that a new
chemical substance or significant new use is not likely to present an
unreasonable risk of injury to health or the environment. Such
statements apply to premanufacture notices (PMNs), microbial commercial
activity notices (MCANs), and significant new use notices (SNUNs)
submitted to EPA under TSCA. This document presents statements of
findings made by EPA on such submissions during the period from May 1,
2022 to July 31, 2022.
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPPT-2022-0116, is available online
at https://www.regulations.gov or in-person at the Office of Pollution
Prevention and Toxics Docket (OPPT Docket), Environmental Protection
Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg.,
Rm. 3334, 1301 Constitution Ave. NW, Washington, DC. 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 OPPT Docket is
(202) 566-0280. 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:
Rebecca Edelstein, New Chemical Division (7405M), Office of Pollution
Prevention and Toxics, Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC 20460-0001; telephone number:
(202) 564-1667; email address: [email protected].
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; email address: [email protected].
SUPPLEMENTARY INFORMATION:
I. Executive Summary
A. Does this action apply to me?
This action provides information that is directed to the public in
general.
B. What action is the Agency taking?
This document lists the statements of findings made by EPA after
review of submissions under TSCA section 5(a) that certain new chemical
substances or significant new uses are not likely to present an
unreasonable risk of injury to health or the environment. This document
presents statements of findings made by EPA during the reporting
period.
C. What is the Agency's authority for taking this action?
TSCA section 5(a)(3) requires EPA to review a submission under TSCA
section 5(a) and make one of the following specific findings:
The chemical substance or significant new use presents an
unreasonable risk of injury to health or the environment;
The information available to EPA is insufficient to permit
a reasoned evaluation of the health and environmental effects of the
chemical substance or significant new use;
The information available to EPA is insufficient to permit
a reasoned evaluation of the health and environmental effects and the
chemical substance or significant new use may present an unreasonable
risk of injury to health or the environment;
The chemical substance is or will be produced in
substantial quantities, and such substance either enters or may
reasonably be anticipated to enter the environment in substantial
quantities or there is or may be significant or substantial human
exposure to the substance; or
The chemical substance or significant new use is not
likely to present an unreasonable risk of injury to health or the
environment.
Under TSCA, the unreasonable risk findings must be made without
consideration of costs or other non-risk factors, including an
unreasonable risk to a potentially exposed or susceptible subpopulation
identified as relevant under the conditions of use. The term
``conditions of use'' is defined in TSCA section 3 to mean ``the
circumstances, as determined by the Administrator, under which a
chemical substance is intended, known, or reasonably foreseen to be
manufactured, processed, distributed in commerce, used, or disposed
of.''
TSCA section 5(g) requires EPA to publish in the Federal Register a
statement of its findings after its review of a submission under TSCA
section 5(a) when EPA makes a finding that a new chemical substance or
significant new use is not likely to present an unreasonable risk of
injury to health or the environment. Such statements apply to PMNs,
MCANs, and SNUNs submitted to EPA under TSCA section 5.
Anyone who plans to manufacture (which includes import) a new
chemical substance for a non-exempt commercial purpose and any
manufacturer or processor wishing to engage in a use of a chemical
substance designated by EPA as a significant new use must submit a
notice to EPA at least 90 days before commencing manufacture of the new
chemical substance or before engaging in the significant new use.
The submitter of a notice to EPA for which EPA has made a finding
of ``not likely to present an unreasonable risk of injury to health or
the environment'' may commence manufacture of the chemical substance or
manufacture or processing for the significant new use notwithstanding
any remaining portion of the applicable review period.
II. Statements of Findings Under TSCA Section 5(a)(3)(C)
In this unit, EPA provides the following information (to the extent
that such information is not claimed as Confidential Business
Information (CBI)) on the PMNs, MCANs and SNUNs for which, during this
period, EPA has made findings under TSCA section 5(a)(3)(C) that the
new chemical substances or significant new uses are not likely to
present an unreasonable risk of injury to health or the environment:
The following list provides the EPA case number assigned to the
TSCA section 5(a) submission and the chemical identity (generic name if
the specific name is claimed as CBI).
J-22-0012, J-22-0013, Genetically modified microorganism
for the production of a chemical substance (Generic Name).
To access EPA's decision document describing the basis of the ``not
likely to present an unreasonable risk'' finding
[[Page 51413]]
made by EPA under TSCA section 5(a)(3)(C), look up the specific case
number at https://www.epa.gov/reviewing-new-chemicals-under-toxic-substances-control-act-tsca/chemicals-determined-not-likely.
Authority: 15 U.S.C. 2601 et seq.
Dated: August 15, 2022.
Madison Le,
Director, New Chemicals Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2022-18011 Filed 8-19-22; 8:45 am]
BILLING CODE 6560-50-P