Pesticide Registration Review; Proposed Decisions for Several Pesticides; Notice of Availability, 6722-6724 [2023-02078]

Download as PDF 6722 Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices the end of your comments. For assistance, please contact FERC Online Support. In lieu of electronic filing, you may submit a paper copy. Submissions sent via the U.S. Postal Service must be addressed to: Kimberly D. Bose, Secretary, Federal Energy Regulatory Commission, 888 First Street NE, Room 1A, Washington, DC 20426. Submissions sent via any other carrier must be addressed to: Kimberly D. Bose, Secretary, Federal Energy Regulatory Commission, 12225 Wilkins Avenue, Rockville, Maryland 20852. The first page of any filing should include docket number P–15270. More information about this project, including a copy of the application, can be viewed or printed on the ‘‘eLibrary’’ link of Commission’s website at https:// www.ferc.gov/docs-filing/elibrary.asp. Enter the docket number (P–15270) in the docket number field to access the document. For assistance, contact FERC Online Support. Dated: January 26, 2023. Debbie-Anne A. Reese, Deputy Secretary. [FR Doc. 2023–02087 Filed 1–31–23; 8:45 am] BILLING CODE 6717–01–P DEPARTMENT OF ENERGY Federal Energy Regulatory Commission [Project No. 11286–028] lotter on DSK11XQN23PROD with NOTICES1 City of Abbeville; Notice of Intent To File License Application, Filing of PreApplication Document, and Approving Use of the Traditional Licensing Process a. Type of Filing: Notice of Intent to File License Application and Request to Use the Traditional Licensing Process (TLP). b. Project No.: 11286–028. c. Dated Filed: November 29, 2022. d. Submitted By: City of Abbeville. e. Name of Project: Abbeville Hydroelectric Project. f. Location: On the Rocky River in Abbeville and Anderson Counties, South Carolina. No federal lands are occupied by the project works or located within the project boundary. g. Filed Pursuant to: 18 CFR 5.3 of the Commission’s regulations. h. Applicant Contact: Tim Hall, Director of Public Utilities, City of Abbeville, 306 Cambridge Street, Abbeville, SC 29620; Phone: (864) 366– 5058, Email: thall@abbevillecitysc.com. i. FERC Contact: Kristine Sillett at (202) 502–6575 or kristine.sillett@ ferc.gov. VerDate Sep<11>2014 21:04 Jan 31, 2023 Jkt 259001 j. The City of Abbeville filed its request to use the TLP on November 29, 2022. The City of Abbeville provided public notice of its request on November 30, 2022. In a letter dated January 26, 2023, the Director of the Division of Hydropower Licensing approved the City of Abbeville’s request to use the TLP. k. With this notice, we are initiating informal consultation with the U.S. Fish and Wildlife Service and/or NOAA Fisheries under section 7 of the Endangered Species Act and the joint agency regulations thereunder at 50 CFR, Part 402; and NOAA Fisheries under section 305(b) of the MagnusonStevens Fishery Conservation and Management Act and implementing regulations at 50 CFR 600.920. We are also initiating consultation with the South Carolina State Historic Preservation Officer, as required by section 106, National Historic Preservation Act, and the implementing regulations of the Advisory Council on Historic Preservation at 36 CFR 800.2. l. With this notice, we are designating the City of Abbeville as the Commission’s non-federal representative for carrying out informal consultation, pursuant to section 7 of the Endangered Species Act and section 305(b) of the Magnuson-Stevens Fishery Conservation and Management Act; and consultation pursuant to section 106 of the National Historic Preservation Act. m. The City of Abbeville filed a PreApplication Document (PAD; including a proposed process plan and schedule) with the Commission, pursuant to 18 CFR 5.6 of the Commission’s regulations. n. A copy of the PAD may be viewed on the Commission’s website (https:// www.ferc.gov), using the ‘‘eLibrary’’ link. Enter the docket number, excluding the last three digits in the docket number field to access the document. For assistance, contact FERC Online Support at FERCONlineSupport@ferc.gov, (866) 208–3676 (toll free), or (202) 502–8659 (TTY). o. The licensee states its unequivocal intent to submit an application for a new license for Project No. 11286. Pursuant to 18 CFR 16.8, 16.9, and 16.10 each application for a new license and any competing license applications must be filed with the Commission at least 24 months prior to the expiration of the existing license. All applications for license for this project must be filed by November 30, 2025. p. Register online at https:// ferconline.ferc.gov/eSubscription.aspx to be notified via email of new filing and issuances related to this or other PO 00000 Frm 00027 Fmt 4703 Sfmt 4703 pending projects. For assistance, contact FERC Online Support. Dated: January 26, 2023. Debbie-Anne A. Reese, Deputy Secretary. [FR Doc. 2023–02089 Filed 1–31–23; 8:45 am] BILLING CODE 6717–01–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPP–2017–0750; FRL–10527–01– OCSPP] Pesticide Registration Review; Proposed Decisions for Several Pesticides; Notice of Availability Environmental Protection Agency (EPA). AGENCY: ACTION: Notice. This notice announces the availability of EPA’s proposed interim and final registration review decisions and opens a 60-day public comment period on the proposed decisions for the following pesticides: coat protein gene of plum pox virus, dioctyl sodium sulfosuccinate, isopropyl myristate, polymeric betaine, undecylenic acid. SUMMARY: Comments must be received on or before April 3, 2023. DATES: Submit your comments, identified by docket identification (ID) number EPA–HQ–OPP–2017–0750, through 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 and visiting the docket, along with more information about dockets generally, is available at https://www.epa.gov/dockets. ADDRESSES: 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 information 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: (202) 566–0701; email address: biscoe.melanie@epa.gov. SUPPLEMENTARY INFORMATION: E:\FR\FM\01FEN1.SGM 01FEN1 Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices I. General Information A. Does this action apply to me? This action is directed to the public in general and may be of interest to a wide range of stakeholders including environmental, human health, farm worker, and agricultural advocates; the chemical industry; pesticide users; and members of the public interested in the sale, distribution, or use of pesticides. Since others also may be interested, the Agency has not attempted to describe all the specific entities that may be affected by this action. If you have any questions regarding the applicability of this action to a particular entity, consult the Chemical Review Manager for the pesticide of interest 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 on 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 proposed interim or final decisions for all pesticides listed in Table 1 in Unit IV. Through this program, EPA is ensuring that each 6723 pesticide’s registration is based on current scientific and other knowledge, including its effects on human health and the environment. III. Authority EPA is conducting its registration review of the chemicals listed in the Table 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 proposed interim or final registration review decisions for the pesticides shown in Table 1 and opens a 60-day public comment period on the proposed interim and proposed final registration review decisions. lotter on DSK11XQN23PROD with NOTICES1 TABLE 1—PROPOSED INTERIM AND PROPOSED FINAL DECISIONS Registration review case name and No. Docket ID No. Coat Protein Gene of Plum Pox Virus, Case Number 6601. Dioctyl sodium sulfosuccinate, Case 4095. Isopropyl Myristate, Case Number 6315. Polymeric betaine, Case Number 5116. Undecylenic acid, Case 4095 ......... EPA–HQ–OPP–2022–0410 ........... Michael Glikes, glikes.michael@epa.gov, (703) 231–6499. EPA–HQ–OPP–2022–0550 ........... Robert Little, little.robert@epa.gov, (202) 566–2234. EPA–HQ–OPP–2022–0842 ........... Hannah Dean, dean.hannah@epa.gov, (202) 566–2969. EPA–HQ–OPP–2013–0374 ........... Erin Dandridge, dandridge.erin@epa.gov, (202) 566–0635. EPA–HQ–OPP–2022–0549 ........... Robert Little, little.robert@epa.gov, (202) 566–2234. The registration review docket for a pesticide includes earlier documents related to the registration review case. For example, the review opened with a Preliminary Work Plan, for public comment. A Final Work Plan was placed in the docket following public comment on the Preliminary Work Plan. The documents in the dockets describe EPA’s rationales for conducting additional risk assessments for the VerDate Sep<11>2014 21:04 Jan 31, 2023 Jkt 259001 Chemical review manager and contact information registration review of the pesticides included in Table 1 in Unit IV, as well as the Agency’s subsequent risk findings and consideration of possible risk mitigation measures. These proposed interim and proposed final registration review decisions are supported by the rationales included in those documents. Following public comment, the Agency will issue interim or final registration PO 00000 Frm 00028 Fmt 4703 Sfmt 4703 review decisions for the pesticides listed in Table 1 in Unit IV. The registration review final rule at 40 CFR 155.58(a) provides for a minimum 60-day public comment period on all proposed registration review decisions. This comment period is intended to provide an opportunity for public input and a mechanism for initiating any necessary amendments to the proposed decision. All comments should be E:\FR\FM\01FEN1.SGM 01FEN1 6724 Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices submitted using the methods in ADDRESSES and must be received by EPA on or before the closing date. These comments will become part of the docket for the pesticides included in the Tables in Unit IV. Comments received after the close of the comment period will be marked ‘‘late.’’ EPA is not required to consider these late comments. The Agency will carefully consider all comments received by the closing date and may provide a ‘‘Response to Comments Memorandum’’ in the docket. The interim or final registration review decision will explain the effect that any comments had on the decision and provide the Agency’s response to significant comments. Background on the registration review program is provided at: https:// www.epa.gov/pesticide-reevaluation. Authority: 7 U.S.C. 136 et seq. Dated: January 23, 2023. Mary Elissa Reaves, Director, Pesticide Re-Evaluation Division, Office of Pesticide Programs. [FR Doc. 2023–02078 Filed 1–31–23; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPPT–2022–0116; FRL–9412–18– OCSPP] Certain New Chemicals or Significant New Uses; Statements of Findings for October and November 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 October 1, 2022 to November 30, 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 lotter on DSK11XQN23PROD with NOTICES1 SUMMARY: VerDate Sep<11>2014 21:04 Jan 31, 2023 Jkt 259001 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. SUPPLEMENTARY INFORMATION: 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. I. Executive Summary 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–22–0017, J–22–0018, Microorganisms transformed to express an enzyme (Generic Name). • J–22–0021, Genetically modified microorganism for the production of a chemical substance (Generic Name). • P–21–0174, Carbonic acid, ester, polymer with alkanediol (C=4,5) (Generic 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/newchemicals-under-toxic-substances- 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 PO 00000 Frm 00029 Fmt 4703 Sfmt 4703 D. Does this action have any incremental economic impacts or paperwork burdens? No. E:\FR\FM\01FEN1.SGM 01FEN1

Agencies

ENVIRONMENTAL PROTECTION AGENCY

[Federal Register Volume 88, Number 21 (Wednesday, February 1, 2023)]
[Notices]
[Pages 6722-6724]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-02078]


=======================================================================
-----------------------------------------------------------------------

ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPP-2017-0750; FRL-10527-01-OCSPP]


Pesticide Registration Review; Proposed Decisions for Several 
Pesticides; Notice of Availability

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: This notice announces the availability of EPA's proposed 
interim and final registration review decisions and opens a 60-day 
public comment period on the proposed decisions for the following 
pesticides: coat protein gene of plum pox virus, dioctyl sodium 
sulfosuccinate, isopropyl myristate, polymeric betaine, undecylenic 
acid.

DATES: Comments must be received on or before April 3, 2023.

ADDRESSES: Submit your comments, identified by docket identification 
(ID) number EPA-HQ-OPP-2017-0750, through 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 and visiting the docket, along with more 
information about dockets generally, is available at https://www.epa.gov/dockets.

FOR FURTHER INFORMATION CONTACT: 
    For pesticide specific information, contact: The Chemical Review 
Manager for the pesticide of interest identified in Table 1 in Unit IV.
    For general information 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: 
(202) 566-0701; email address: [email protected].

SUPPLEMENTARY INFORMATION:

[[Page 6723]]

I. General Information

A. Does this action apply to me?

    This action is directed to the public in general and may be of 
interest to a wide range of stakeholders including environmental, human 
health, farm worker, and agricultural advocates; the chemical industry; 
pesticide users; and members of the public interested in the sale, 
distribution, or use of pesticides. Since others also may be 
interested, the Agency has not attempted to describe all the specific 
entities that may be affected by this action. If you have any questions 
regarding the applicability of this action to a particular entity, 
consult the Chemical Review Manager for the pesticide of interest 
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 on 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 proposed interim or final decisions for all 
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 the 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 proposed interim or final registration review decisions for 
the pesticides shown in Table 1 and opens a 60-day public comment 
period on the proposed interim and proposed final registration review 
decisions.

         Table 1--Proposed Interim and Proposed Final Decisions
------------------------------------------------------------------------
                                                      Chemical review
 Registration review case name    Docket ID No.     manager and contact
            and No.                                     information
------------------------------------------------------------------------
Coat Protein Gene of Plum Pox   EPA-HQ-OPP-2022-0  Michael Glikes,
 Virus, Case Number 6601.        410.               [email protected], (703) 231-6499.
Dioctyl sodium sulfosuccinate,  EPA-HQ-OPP-2022-0  Robert Little,
 Case 4095.                      550.               [email protected], (202) 566-2234.
Isopropyl Myristate, Case       EPA-HQ-OPP-2022-0  Hannah Dean,
 Number 6315.                    842.               [email protected],
                                                    (202) 566-2969.
Polymeric betaine, Case Number  EPA-HQ-OPP-2013-0  Erin Dandridge,
 5116.                           374.               [email protected], (202) 566-0635.
Undecylenic acid, Case 4095...  EPA-HQ-OPP-2022-0  Robert Little,
                                 549.               [email protected], (202) 566-2234.
------------------------------------------------------------------------

    The registration review docket for a pesticide includes earlier 
documents related to the registration review case. For example, the 
review opened with a Preliminary Work Plan, for public comment. A Final 
Work Plan was placed in the docket following public comment on the 
Preliminary Work Plan.
    The documents in the dockets describe EPA's rationales for 
conducting additional risk assessments for the registration review of 
the pesticides included in Table 1 in Unit IV, as well as the Agency's 
subsequent risk findings and consideration of possible risk mitigation 
measures. These proposed interim and proposed final registration review 
decisions are supported by the rationales included in those documents. 
Following public comment, the Agency will issue interim or final 
registration review decisions for the pesticides listed in Table 1 in 
Unit IV.
    The registration review final rule at 40 CFR 155.58(a) provides for 
a minimum 60-day public comment period on all proposed registration 
review decisions. This comment period is intended to provide an 
opportunity for public input and a mechanism for initiating any 
necessary amendments to the proposed decision. All comments should be

[[Page 6724]]

submitted using the methods in ADDRESSES and must be received by EPA on 
or before the closing date. These comments will become part of the 
docket for the pesticides included in the Tables in Unit IV. Comments 
received after the close of the comment period will be marked ``late.'' 
EPA is not required to consider these late comments.
    The Agency will carefully consider all comments received by the 
closing date and may provide a ``Response to Comments Memorandum'' in 
the docket. The interim or final registration review decision will 
explain the effect that any comments had on the decision and provide 
the Agency's response to significant comments.
    Background on the registration review program is provided at: 
https://www.epa.gov/pesticide-reevaluation.
    Authority: 7 U.S.C. 136 et seq.

    Dated: January 23, 2023.
Mary Elissa Reaves,
Director, Pesticide Re-Evaluation Division, Office of Pesticide 
Programs.
[FR Doc. 2023-02078 Filed 1-31-23; 8:45 am]
BILLING CODE 6560-50-P

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