2020-18598. Coumaphos; Revised Proposed Interim Registration Review Decision; Notice of Availability  

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    AGENCY:

    Environmental Protection Agency (EPA).

    ACTION:

    Notice.

    SUMMARY:

    This notice announces the availability of and solicits public comment on EPA's revised proposed interim registration review decision for coumaphos.

    DATES:

    Comments must be received on or before October 26, 2020.

    ADDRESSES:

    Submit your comments, identified by the docket identification (ID) number for the specific pesticide of interest provided in the Table in Unit IV., using the Federal eRulemaking Portal at http://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.

    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.

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    FOR FURTHER INFORMATION CONTACT:

    For pesticide specific information, contact: The Chemical Review Manager for the pesticide of interest identified in the Table 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: (703) 305-7106; email address: biscoe.melanie@epa.gov.

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    SUPPLEMENTARY INFORMATION:

    I. General Information

    A. Does this action apply to me?

    This action is directed to the public in general, and may be of interest to a wide range of stakeholders including environmental, human health, farm worker, and agricultural advocates; the 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 pesticide specific contact person listed under FOR FURTHER INFORMATION CONTACT: For pesticide specific information, contact: The Chemical Review Manager for the pesticide of interest identified in the Table 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: (703) 305-7106; email address: biscoe.melanie@epa.gov.

    B. What should I consider as I prepare my comments for EPA?

    1. Submitting CBI. Do not submit this information to EPA through Start Printed Page 52342 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 http://www.epa.gov/​dockets/​comments.html.

    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 the revised proposed interim decisions for coumaphos listed in the Table 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 coumaphos 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 revised proposed interim registration review decisions for coumaphos. The revised proposed interim registration review decision is supported by rationale included in the docket established for each chemical.

    Table—Registration Review Proposed Interim Decisions Being Issued

    Registration review case name and No.Docket ID No.Chemical review manager and contact information
    Coumaphos (Case0018)EPA-HQ-OPP-2008-0023Michelle Nolan, nolan.michelle@epa.gov, (703) 347-0258.

    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 coumaphos, as well as the Agency's subsequent risk findings and consideration of possible risk mitigation measures. This revised proposed interim registration review decision is supported by the rationales included in those documents. Following public comment, the Agency will issue an interim or final registration review decision for coumaphos.

    The registration review final rule at 40 CFR 155.58(a) provides for a minimum 60-day public comment period on all proposed interim 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 interim decision. All comments should be 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 coumaphos. Comments received after the close of the comment period will be marked “late.” EPA is not required to consider these late comments.

    The proposed interim registration review decision for coumaphos was posted to the docket in May 2018 and the public was invited to submit any comments or new information during the 60-day comment period. A comment extension request was submitted by Bayer Animal Health which resulted in a 30-day extension or 90-day total comment period. Comments from the 90-day comment period that were received were considered and affected the Agency's revised proposed interim decision. EPA addressed the comments or information received during the 90-day comment period for the proposed interim decision and is issuing a revised proposed interim decision for a 60-day comment period. Pursuant to 40 CFR 155.58(c), the registration review case docket for the chemicals listed in the Table will remain open until all actions required in the proposed interim decision have been completed.

    Background on the registration review program is provided at: http://www.epa.gov/​pesticide-reevaluation.

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    Authority: 7 U.S.C. 136 et seq.

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    Dated: August 14, 2020.

    Mary Reaves,

    Acting Director, Pesticide Re-Evaluation Division, Office of Pesticide Programs.

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    [FR Doc. 2020-18598 Filed 8-24-20; 8:45 am]

    BILLING CODE 6560-50-P

Document Information

Published:
08/25/2020
Department:
Environmental Protection Agency
Entry Type:
Notice
Action:
Notice.
Document Number:
2020-18598
Dates:
Comments must be received on or before October 26, 2020.
Pages:
52341-52342 (2 pages)
Docket Numbers:
EPA-HQ-OPP-2017-0751, FRL-10013-81
PDF File:
2020-18598.pdf
Supporting Documents:
» Coumaphos: Response to Comments on the Human Health Risk Assessment for Registration Review
» Risk Mitigation Discussion with Coumaphos Registrant 6-25-2021
» Authorization to Extend the Public Comment Period for the Revised Proposed Interim Decision for the Registration Review of Coumaphos
» Coumaphos Revised Proposed Interim Registration Review Decision Case Number 0018
» Revised Proposed Interim Registration Review Decision: Coumaphos
» Memorandum for Extension of Comment Period for Coumaphos Preliminary Interim Decision( PID)
» Organophosphates: Response to Endocrine Disruptor Screening Program (EDSP) Comments on the Preliminary Organophosphate Human Health Risk Assessments. December 22, 2016.
» Organophosphates: Response to Dietary-Related Comments on the Preliminary Organophosphate Human Health Risk Assessments. DP Barcode: D437199. December 22, 2016.
» Summary of EPA Meetings with Non-EPA Entities Regarding the Registration Review of Coumaphos. April 23, 2018.
» BEAD Estimate of the Percent Crop Treated (PCT) for Coumaphos Use on Cattle for Dietary Assessment (PC Code: 036501). October 7, 2016.