Certain New Chemicals or Significant New Uses; Statements of Findings for August 2021, 58908-58910 [2021-23190]
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58908
Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices
TABLE 3—REGISTRANTS REQUESTING VOLUNTARY CANCELLATION AND/OR AMENDMENTS
EPA company No.
Company name and address
100 ..................................................
279 ..................................................
2693 ................................................
9688 ................................................
Syngenta Crop Protection, LLC, 410 Swing Road, P.O. Box 18300, Greensboro, NC 27419–8300.
FMC Corporation, 2929 Walnut Street, Philadelphia, PA 19104.
International Paint, LLC, 6001 Antoine Drive, Houston, TX 77091.
Chemsico, A Division of United Industries Corp., One Rider Trail Plaza Drive, Suite 300, Earth City, MO
63045–1313.
Drexel Chemical Company, P.O. Box 13327, Memphis, TN 38113–0327.
Winfield Solutions, LLC, P.O. Box 64589, St. Paul, MN 55164–0589.
Loveland Products, Inc., P.O. Box 1286, Greeley, CO 80632–1286.
Albaugh, LLC, 1525 NE 36th Street, Ankeny, IA 50021.
Tenkoz, Inc., 1725 Windward Concourse, Suite 410, Alpharetta, GA 30005.
Corteva Agriscience, LLC, 9330 Zionsville Road, Indianapolis, IN 46268.
Multi-Chem Group, LLC—Odessa, 6155 W Murphy St., Odessa, TX 79763–7511.
19713
33270
34704
42750
55467
62719
71173
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III. What is the Agency’s authority for
taking this action?
V. Provisions for Disposition of Existing
Stocks
Section 6(f)(1) of FIFRA (7 U.S.C.
136d(f)(1)) provides that a registrant of
a pesticide product may at any time
request that any of its pesticide
registrations be canceled or amended to
terminate one or more uses. FIFRA
further provides that, before acting on
the request, EPA must publish a notice
of receipt of any such request in the
Federal Register.
Section 6(f)(1)(B) of FIFRA (7 U.S.C.
136d(f)(1)(B)) requires that before acting
on a request for voluntary cancellation,
EPA must provide a 30-day public
comment period on the request for
voluntary cancellation or use
termination. In addition, FIFRA section
6(f)(1)(C) (7 U.S.C. 136d(f)(1)(C))
requires that EPA provide a 180-day
comment period on a request for
voluntary cancellation or termination of
any minor agricultural use before
granting the request, unless:
1. The registrants request a waiver of
the comment period, or
2. The EPA Administrator determines
that continued use of the pesticide
would pose an unreasonable adverse
effect on the environment.
The registrants have requested that
EPA waive the 180-day comment
period. Accordingly, EPA will provide a
30-day comment period on the proposed
requests.
Existing stocks are those stocks of
registered pesticide products that are
currently in the United States and that
were packaged, labeled, and released for
shipment prior to the effective date of
the action. If the requests for voluntary
cancellation and amendments to
terminate uses are granted, the Agency
intends to publish the cancellation
order in the Federal Register.
In any order issued in response to
these requests for cancellation of
product registrations and amendments
to terminate uses, EPA proposes to
include the following provisions for the
treatment of any existing stocks of the
products listed in Table 1, Table 1A and
Table 2 of Unit II.
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IV. Procedures for Withdrawal of
Requests
Registrants who choose to withdraw a
request for product cancellation or use
termination should submit the
withdrawal in writing to the person
listed under FOR FURTHER INFORMATION
CONTACT. If the products have been
subject to a previous cancellation
action, the effective date of cancellation
and all other provisions of any earlier
cancellation action are controlling.
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For Product 100–1431
For product 100–1431 listed in Table
1A of Unit II, the registrant has
requested March 30, 2022, as the
effective date of cancellation, registrants
will be permitted to sell and distribute
existing stocks of voluntarily canceled
products for 1 year after the effective
date of the cancellation, which will be
March 30, 2023. Thereafter, registrants
will be prohibited from selling or
distributing the product identified in
Table 1A of Unit II, except for export
consistent with FIFRA section 17 (7
U.S.C. 136o) or for proper disposal.
For all other voluntary product
cancellations, listed in Table 1 of Unit
II, registrants will be permitted to sell
and distribute existing stocks of
voluntarily canceled products for 1 year
after the effective date of the
cancellation, which will be the date of
publication of the cancellation order in
the Federal Register. Thereafter,
registrants will be prohibited from
selling or distributing the products
identified in Table 1 of Unit II, except
for export consistent with FIFRA section
17 (7 U.S.C. 136o) or for proper
disposal.
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Once EPA has approved product
labels reflecting the requested
amendments to terminate uses,
registrants will be permitted to sell or
distribute products under the previously
approved labeling for a period of 18
months after the date of Federal
Register publication of the cancellation
order, unless other restrictions have
been imposed. Thereafter, registrants
will be prohibited from selling or
distributing the products whose labels
include the terminated uses identified
in Table 2 of Unit II, except for export
consistent with FIFRA section 17 or for
proper disposal.
Persons other than the registrant may
sell, distribute, or use existing stocks of
canceled products & products whose
labels include the terminated uses until
supplies are exhausted, provided that
such sale, distribution, or use is
consistent with the terms of the
previously approved labeling on, or that
accompanied, the canceled products &
terminated uses.
Authority: 7 U.S.C. 136 et seq.
Dated: October 15, 2021.
Marietta Echeverria,
Acting Director, Registration Division, Office
of Pesticide Programs.
[FR Doc. 2021–23178 Filed 10–22–21; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2021–0146; FRL–8682–05–
OCSPP]
Certain New Chemicals or Significant
New Uses; Statements of Findings for
August 2021
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
SUMMARY:
E:\FR\FM\25OCN1.SGM
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Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices
jspears on DSK121TN23PROD with NOTICES1
notices 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 August 1, 2021 to August 31, 2021.
FOR FURTHER INFORMATION CONTACT: For
technical information contact: Rebecca
Edelstein, Chemical Control 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:
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:
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. What action is the Agency taking?
This document lists the statements of
findings made by EPA after review of
notices submitted 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 period from August 1, 2021
to August 31, 2021.
III. What is the Agency’s authority for
taking this action?
TSCA section 5(a)(3) requires EPA to
review a TSCA section 5(a) notice 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;
I. General Information
• The information available to EPA is
A. Does this action apply to me?
insufficient to permit a reasoned
evaluation of the health and
This action is directed to the public
environmental effects of the chemical
in general. As such, the Agency has not
substance or significant new use;
attempted to describe the specific
• The information available to EPA is
entities that this action may apply to.
insufficient to permit a reasoned
Although others may be affected, this
action applies directly to the submitters evaluation of the health and
environmental effects and the chemical
of the PMNs addressed in this action.
substance or significant new use may
B. How can I get copies of this document present an unreasonable risk of injury to
and other related information?
health or the environment;
• The chemical substance is or will
The docket for this action, identified
be produced in substantial quantities,
by docket identification (ID) number
EPA–HQ–OPPT–2021–0146, is available and such substance either enters or may
reasonably be anticipated to enter the
at https://www.regulations.gov or at the
environment in substantial quantities or
Office of Pollution Prevention and
there is or may be significant or
Toxics Docket (OPPT Docket),
substantial human exposure to the
Environmental Protection Agency
substance; or
Docket Center (EPA/DC), West William
• The chemical substance or
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC. significant new use is not likely to
present an unreasonable risk of injury to
The Public Reading Room is open from
health or the environment.
8:30 a.m. to 4:30 p.m., Monday through
Unreasonable risk findings must be
Friday, excluding legal holidays. The
made without consideration of costs or
telephone number for the Public
other non-risk factors, including an
Reading Room is (202) 566–1744, and
unreasonable risk to a potentially
the telephone number for the OPPT
exposed or susceptible subpopulation
Docket is (202) 566–0280.
identified as relevant under the
Due to the public health concerns
conditions of use. The term ‘‘conditions
related to COVID–19, the EPA Docket
of use’’ is defined in TSCA section 3 to
Center (EPA/DC) and Reading Room is
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58909
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.’’
EPA is required under TSCA section
5(g) to publish in the Federal Register
a statement of its findings after its
review of a TSCA section 5(a) notice
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.
IV. Statements of Administrator
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:
• EPA case number assigned to the
TSCA section 5(a) notice.
• Chemical identity (generic name if
the specific name is claimed as CBI).
• website link to EPA’s decision
document describing the basis of the
‘‘not likely to present an unreasonable
risk’’ finding made by EPA under TSCA
section 5(a)(3)(C).
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Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices
EPA Case No.
Chemical identity
P–20–0148, .....................................
P–20–0149, .....................................
P–20–0150, .....................................
P–20–0151 ......................................
Hydroxyalkanoic acid, salt,
oxidized (Generic Name).
Authority: 15 U.S.C. 2601 et seq.
Dated: October 19, 2021.
Madison Le,
Director, New Chemicals Division, Office of
Pollution Prevention and Toxics.
[FR Doc. 2021–23190 Filed 10–22–21; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2020–0692; 9179–01–OMS]
Information Collection Request
Submitted to OMB for Review and
Approval; Comment Request;
Pesticide Environmental Stewardship
Program Annual Measures Reporting
(Renewal)
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The Environmental Protection
Agency (EPA) has submitted an
information collection request (ICR),
Pesticide Environmental Stewardship
Program Annual Measures Reporting,
(EPA ICR Number 2415.04, OMB
Control Number 2070–0188) to the
Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act. This is a proposed
extension of the ICR, which is currently
approved through October 31, 2021.
Public comments were previously
requested via the Federal Register on
March 31, 2021 during a 60-day
comment period. This notice allows for
an additional 30 days for public
comments. A fuller description of the
ICR is given below, including its
estimated burden and cost to the public.
An agency may not conduct or sponsor
and a person is not required to respond
to a collection of information unless it
displays a currently valid OMB control
number.
DATES: Additional comments may be
submitted on or before November 24,
2021.
ADDRESSES: Submit your comments to
EPA, referencing Docket ID No. EPA–
HQ–OPP–2020–0692, online using
www.regulations.gov (our preferred
method), by email to siu.carolyn@
epa.gov, or by mail to: EPA Docket
Center, Environmental Protection
jspears on DSK121TN23PROD with NOTICES1
SUMMARY:
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Website link
https://www.epa.gov/system/files/documents/2021-09/p-20-01480151_determination_non-cbi_final_0.pdf.
Agency, Mail Code 28221T, 1200
Pennsylvania Ave. NW, Washington, DC
20460. EPA’s policy is that all
comments received will be included in
the public docket without change
including any personal information
provided, unless the comment includes
profanity, threats, information claimed
to be Confidential Business Information
(CBI), or other information whose
disclosure is restricted by statute.
Submit written comments and
recommendations to OMB for the
proposed information collection within
30 days of publication of this notice to
www.reginfo.gov/public/do/PRAMain.
Find this particular information
collection by selecting ‘‘Currently under
30-day Review—Open for Public
Comments’’ or by using the search
function.
FOR FURTHER INFORMATION CONTACT:
Carolyn Siu, Mission Support Division
(7101M), Office of Program Support,
Office of Chemical Safety and Pollution
Prevention, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460; telephone
number: (703) 347–0159; email address:
siu.carolyn@epa.gov.
SUPPLEMENTARY INFORMATION:
Supporting documents which explain in
detail the information that the EPA will
be collecting are available in the public
docket for this ICR. The docket 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 ICR covers the
information collection activities
associated with voluntary participation
in EPA’s Pesticide Environmental
Stewardship Program (PESP). The
program uses the information collected
to establish partner membership,
develop stewardship strategies, measure
progress towards stewardship goals, and
award incentives. PESP is an EPA
partnership program that encourages the
use of the integrated pest management
(IPM) strategies to reduce pests and
pesticide risks. IPM is an approach that
involves making the best choices from
among a series of pest management
practices that are both economical and
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pose the least possible hazard to people,
property, and the environment.
PESP members include pesticide enduser and organizations which focus on
training, educating, and/or influencing
pesticide users. To become a PESP
member, an organization submits an
application and a five-year strategy
outlining how environmental and
human health risk reduction goals will
be achieved through IPM
implementation and/or education. The
program encourages PESP members to
track progress towards IPM goals such
as: reductions in unnecessary use of
pesticides, cost reductions, and
knowledge shared about IPM
methodologies. Entities participating in
PESP also benefit from technical
assistance, and through incentives for
achievements at different levels.
Form Numbers: 9600–01, 9600–02,
and 9600–03.
Respondents/affected entities:
Pesticide user companies and
organizations, or entities that practice
IPM or promote the use of IPM through
education and training.
Respondent’s obligation to respond:
Voluntary (5 CFR 1320.5(d)(2)).
Estimated number of respondents:
461 (total).
Frequency of response: Annual and
on occasion.
Total estimated burden: 51,562 hours
(per year). Burden is defined at 5 CFR
1320.03(b).
Total estimated cost: $3,605,562 (per
year), includes $0 annualized capital or
operation & maintenance costs.
Changes in the Estimates: There is a
correction of the number of potential
respondents from 419 to 461. There is
an increase of 3,897 hours in the total
estimated respondent burden compared
with the ICR currently approved by
OMB. This increase reflects EPA’s
updating of burden estimates for this
collection based on historical
information on the number of PESP
members. Based on revised estimates,
the number of IPM Promoters has
decreased, while the number of IPM
users has increased, and the number of
National IPM users has decreased since
the last ICR renewal. Although the
estimated burden per response has not
changed for any category, the shift in
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Agencies
[Federal Register Volume 86, Number 203 (Monday, October 25, 2021)]
[Notices]
[Pages 58908-58910]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-23190]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2021-0146; FRL-8682-05-OCSPP]
Certain New Chemicals or Significant New Uses; Statements of
Findings for August 2021
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
[[Page 58909]]
notices 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 August 1, 2021 to August 31, 2021.
FOR FURTHER INFORMATION CONTACT: For technical information contact:
Rebecca Edelstein, Chemical Control 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. General Information
A. Does this action apply to me?
This action is directed to the public in general. As such, the
Agency has not attempted to describe the specific entities that this
action may apply to. Although others may be affected, this action
applies directly to the submitters of the PMNs addressed in this
action.
B. How can I get copies of this document and other related information?
The docket for this action, identified by docket identification
(ID) number EPA-HQ-OPPT-2021-0146, is available at https://www.regulations.gov or 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.
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. What action is the Agency taking?
This document lists the statements of findings made by EPA after
review of notices submitted 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 period
from August 1, 2021 to August 31, 2021.
III. What is the Agency's authority for taking this action?
TSCA section 5(a)(3) requires EPA to review a TSCA section 5(a)
notice 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.
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.''
EPA is required under TSCA section 5(g) to publish in the Federal
Register a statement of its findings after its review of a TSCA section
5(a) notice 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.
IV. Statements of Administrator 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:
EPA case number assigned to the TSCA section 5(a) notice.
Chemical identity (generic name if the specific name is
claimed as CBI).
website link to EPA's decision document describing the
basis of the ``not likely to present an unreasonable risk'' finding
made by EPA under TSCA section 5(a)(3)(C).
[[Page 58910]]
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EPA Case No. Chemical identity Website link
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P-20-0148,.................... Hydroxyalkanoic https://www.epa.gov/
P-20-0149,.................... acid, salt, system/files/
P-20-0150,.................... oxidized documents/2021-09/p-
P-20-0151..................... (Generic Name). 20-0148-
0151_determination_n
on-cbi_final_0.pdf.
------------------------------------------------------------------------
Authority: 15 U.S.C. 2601 et seq.
Dated: October 19, 2021.
Madison Le,
Director, New Chemicals Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2021-23190 Filed 10-22-21; 8:45 am]
BILLING CODE 6560-50-P