Certain New Chemicals or Significant New Uses; Statements of Findings for December 2022, 16976-16977 [2023-05680]
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16976
Federal Register / Vol. 88, No. 54 / Tuesday, March 21, 2023 / Notices
significant economic impact on a
substantial number of small entities. For
purposes of the RFA, a ‘‘rule’’ does not
include ‘‘a rule of particular
applicability relating to rates [and]
services . . . or to valuations, costs or
accounting, or practices relating to such
rates [and] services . . .’’ 5 U.S.C. 601.
WAPA has determined that this action
relates to services offered by WAPA
and, therefore, is not a rule within the
purview of the RFA.
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2022–0116; FRL–9412–15–
OCSPP]
Signed in Washington, DC, on March 16,
2023.
Treena V. Garrett,
Federal Register Liaison Officer, U.S.
Department of Energy.
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[FR Doc. 2023–05736 Filed 3–20–23; 8:45 am]
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I. Executive Summary
A. Does this action apply to me?
Certain New Chemicals or Significant
New Uses; Statements of Findings for
December 2022
This action provides information that
is directed to the public in general.
Environmental Protection
Agency (EPA).
ACTION: Notice.
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.
AGENCY:
C. Determination Under Executive Order SUMMARY: The Toxic Substances Control
Act (TSCA) requires EPA to publish in
12866
the Federal Register a statement of its
findings after its review of certain TSCA
WAPA has an exemption from
submissions when EPA makes a finding
centralized regulatory review under
Executive Order 12866. Accordingly, no that a new chemical substance or
significant new use is not likely to
clearance of this notice by the Office of
present an unreasonable risk of injury to
Management and Budget is required.
health or the environment. Such
D. Review Under Paperwork Reduction
statements apply to premanufacture
Act
notices (PMNs), microbial commercial
activity notices (MCANs), and
In accordance with the Paperwork
significant new use notices (SNUNs),
Reduction Act (44 U.S.C. 3501, et seq.),
submitted to EPA under TSCA. This
WAPA has received approval from the
document presents statements of
Office of Management and Budget to
findings made by EPA on such
collect applicant data, under OMB
submissions during the period from
control number 1910–5136.
December 1, 2022, to December 31,
2022.
Signing Authority
This document of the Department of
Energy was signed on March 3, 2023, by
Tracey A. LeBeau, Administrator,
Western Area Power Administration,
pursuant to delegated authority from the
Secretary of Energy. That document,
with the original signature and date, is
maintained by DOE. For administrative
purposes only, and in compliance with
requirements of the Office of the Federal
Register, the undersigned DOE Federal
Register Liaison Officer has been
authorized to sign and submit the
document in electronic format for
publication, as an official document of
the Department of Energy. This
administrative process in no way alters
the legal effect of this document upon
publication in the Federal Register.
SUPPLEMENTARY INFORMATION:
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:
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.
ADDRESSES:
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B. What action is the Agency taking?
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 several
specific findings pertaining to whether
the substance may present unreasonable
risk of injury to health or the
environment. Among those potential
findings is that the chemical substance
or significant new use is not likely to
present an unreasonable risk of injury to
health or the environment per TSCA
Section 5(a)(3)(C).
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.
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Federal Register / Vol. 88, No. 54 / Tuesday, March 21, 2023 / Notices
D. Does this action have any
incremental economic impacts or
paperwork burdens?
No.
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–22–0019–0020, Saccharomyces
cerevisiae, chromosomal integration
modification (Generic Name).
• J–22–0022–0025, Microorganisms
stably transformed to manufacture PHA
(Generic Name).
• J–23–0002, Microorganism stably
transformed to express a recombinant
protein (Generic Name).
• P–22–0017, 1-Eicosanol, manuf. of,
distn., residues; CASRN: 2682937–26–2
(Specific Name).
To access 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), 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: March 14, 2023.
Madison Le,
Director, New Chemicals Division, Office of
Pollution Prevention and Toxics.
[FR Doc. 2023–05680 Filed 3–20–23; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL TRADE COMMISSION
ddrumheller on DSK120RN23PROD with NOTICES1
[File No. 211 0182]
Anchor Glass Container Corporation;
Analysis of Agreement Containing
Consent Order To Aid Public Comment
Federal Trade Commission.
Proposed consent agreement;
request for comment.
AGENCY:
ACTION:
The consent agreement in this
matter settles alleged violations of
federal law prohibiting unfair methods
SUMMARY:
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of competition. The attached Analysis of
Proposed Consent Orders to Aid Public
Comment describes both the allegations
in the complaint and the terms of the
consent orders—embodied in the
consent agreement—that would settle
these allegations.
DATES: Comments must be received on
or before April 20, 2023.
ADDRESSES: Interested parties may file
comments online or on paper by
following the instructions in the
Request for Comment part of the
SUPPLEMENTARY INFORMATION section
below. Please write: ‘‘Anchor Glass
Non-compete Restrictions; File No. 211
0182’’ on your comment and file your
comment online at https://
www.regulations.gov by following the
instructions on the web-based form. If
you prefer to file your comment on
paper, please mail your comment to the
following address: Federal Trade
Commission, Office of the Secretary,
600 Pennsylvania Avenue NW, Suite
CC–5610 (Annex Q), Washington, DC
20580.
FOR FURTHER INFORMATION CONTACT:
Kathleen Clair (202–326–3435), Bureau
of Competition, Federal Trade
Commission, 400 7th Street SW,
Washington, DC 20024.
SUPPLEMENTARY INFORMATION: Pursuant
to Section 6(f) of the Federal Trade
Commission Act, 15 U.S.C. 46(f), and
FTC Rule § 2.34, 16 CFR 2.34, notice is
hereby given that the above-captioned
consent agreement containing a consent
order to cease and desist, having been
filed with and accepted, subject to final
approval, by the Commission, has been
placed on the public record for a period
of 30 days. The following Analysis of
Agreement Containing Consent Orders
to Aid Public Comment describes the
terms of the consent agreement and the
allegations in the complaint. An
electronic copy of the full text of the
consent agreement package can be
obtained from the FTC website at this
web address: https://www.ftc.gov/newsevents/commission-actions.
You can file a comment online or on
paper. For the Commission to consider
your comment, we must receive it on or
before April 20, 2023. Write ‘‘Anchor
Glass Non-compete Restrictions; File
No. 211 0182’’ on your comment. Your
comment—including your name and
your state—will be placed on the public
record of this proceeding, including, to
the extent practicable, on the https://
www.regulations.gov website.
Because of the agency’s heightened
security screening, postal mail
addressed to the Commission will be
delayed. We strongly encourage you to
submit your comments online through
PO 00000
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16977
the https://www.regulations.gov
website. If you prefer to file your
comment on paper, write ‘‘Anchor Glass
Non-compete Restrictions; File No. 211
0182’’ on your comment and on the
envelope, and mail your comment to the
following address: Federal Trade
Commission, Office of the Secretary,
600 Pennsylvania Avenue NW, Suite
CC–5610 (Annex Q), Washington, DC
20580.
Because your comment will be placed
on the publicly accessible website at
https://www.regulations.gov, you are
solely responsible for making sure your
comment does not include any sensitive
or confidential information. In
particular, your comment should not
include sensitive personal information,
such as your or anyone else’s Social
Security number; date of birth; driver’s
license number or other state
identification number, or foreign
country equivalent; passport number;
financial account number; or credit or
debit card number. You are also solely
responsible for making sure your
comment does not include sensitive
health information, such as medical
records or other individually
identifiable health information. In
addition, your comment should not
include any ‘‘trade secret or any
commercial or financial information
which . . . is privileged or
confidential’’—as provided by Section
6(f) of the FTC Act, 15 U.S.C. 46(f), and
FTC Rule § 4.10(a)(2), 16 CFR
4.10(a)(2)—including competitively
sensitive information such as costs,
sales statistics, inventories, formulas,
patterns, devices, manufacturing
processes, or customer names.
Comments containing material for
which confidential treatment is
requested must be filed in paper form,
must be clearly labeled ‘‘Confidential,’’
and must comply with FTC Rule
§ 4.9(c). In particular, the written
request for confidential treatment that
accompanies the comment must include
the factual and legal basis for the
request and must identify the specific
portions of the comment to be withheld
from the public record. See FTC Rule
§ 4.9(c). Your comment will be kept
confidential only if the General Counsel
grants your request in accordance with
the law and the public interest. Once
your comment has been posted on
https://www.regulations.gov—as legally
required by FTC Rule § 4.9(b)—we
cannot redact or remove your comment
from that website, unless you submit a
confidentiality request that meets the
requirements for such treatment under
FTC Rule § 4.9(c), and the General
Counsel grants that request.
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Agencies
[Federal Register Volume 88, Number 54 (Tuesday, March 21, 2023)]
[Notices]
[Pages 16976-16977]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-05680]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2022-0116; FRL-9412-15-OCSPP]
Certain New Chemicals or Significant New Uses; Statements of
Findings for December 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
December 1, 2022, to December 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 several specific findings pertaining to
whether the substance may present unreasonable risk of injury to health
or the environment. Among those potential findings is that the chemical
substance or significant new use is not likely to present an
unreasonable risk of injury to health or the environment per TSCA
Section 5(a)(3)(C).
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.
[[Page 16977]]
D. Does this action have any incremental economic impacts or paperwork
burdens?
No.
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-22-0019-0020, Saccharomyces cerevisiae, chromosomal
integration modification (Generic Name).
J-22-0022-0025, Microorganisms stably transformed to
manufacture PHA (Generic Name).
J-23-0002, Microorganism stably transformed to express a
recombinant protein (Generic Name).
P-22-0017, 1-Eicosanol, manuf. of, distn., residues;
CASRN: 2682937-26-2 (Specific Name).
To access 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), 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: March 14, 2023.
Madison Le,
Director, New Chemicals Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2023-05680 Filed 3-20-23; 8:45 am]
BILLING CODE 6560-50-P