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Federal Register / Vol. 86, No. 43 / Monday, March 8, 2021 / 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 identified in the Table 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 in a disk or CDROM that you mail to EPA, mark the outside of the disk or CDROM as CBI and then identify electronically within the disk or CDROM 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.
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 EPAs 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 comprehensive draft human health and/or ecological risk assessments for all pesticides listed in the Table in Unit IV. After reviewing comments received during the public comment period, EPA may issue a revised risk assessment, explain any changes to the draft risk assessment, and respond to comments and may request public input on risk mitigation before
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completing a proposed registration review decision for the pesticides listed in the Table in Unit IV. Through this program, EPA is ensuring that each pesticides 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 in Unit IV pursuant to section 3g of the Federal Insecticide, Fungicide, and Rodenticide Act FIFRA and the Procedural Regulations for Registration Review at 40 CFR part 155, subpart C.
Section 3g 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 3c5 7 U.S.C. 136ac5. 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 EPAs human health and/or ecological risk assessments for the pesticides shown in the following table and opens a 60-day public comment period on the risk assessments.

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TABLEDRAFT RISK ASSESSMENTS BEING MADE AVAILABLE FOR PUBLIC COMMENT
Registration review case name and No.

Docket ID No.

Diuron, Case 0046
Famoxadone, Case 7038
Fluometuron, Case 0049
Indaziflam, Case 7288
Inorganic Chlorates, Case 4049
Mancozeb, Case 0643
Napropamide, Case 2450
Nicarbazin, Case 7628
Peroxy Compounds, Case 6059
Propiconazole, Case 3125
Tetraconazole, Case 7043
Zinc Pyrithione, Case 2480

EPAHQOPP20150077
EPAHQOPP20150094
EPAHQOPP20150746
EPAHQOPP20200587
EPAHQOPP20160080
EPAHQOPP20150291
EPAHQOPP20160019
EPAHQOPP20150101
EPAHQOPP20090546
EPAHQOPP20150459
EPAHQOPP20150061
EPAHQOPP20140158

Pursuant to 40 CFR 155.53c, EPA is providing an opportunity, through this notice of availability, for interested parties to provide comments and input concerning the Agencys draft human health and/or ecological risk
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Chemical review manager and contact information Theodore Varns, varns.theodore@epa.gov, 703 3478589.
Christina Scheltema, scheltema.christina@epa.gov, 703 3082201.
Ana Pinto, pinto.ana@epa.gov, 703 3478421.
Kent Fothergill, fothergill.kent@epa.gov, 703 3478299.
Christian Bongard, bongard.christian@epa.gov, 703 3470337.
Alex Hazlehurst, hazlehurst.alexander@epa.gov, 703 3470221.
Carolyn Smith, smith.carolyn@epa.gov, 703 3478325.
Samantha Thomas, thomas.samantha@epa.gov, 703 3470514.
Joseph Mabon, mabon.joseph@epa.gov, 703 3470177.
Anna Romanovsky, romanovsky.anna@epa.gov, 703 3470203.
Veronica Dutch, dutch.veronica@epa.gov, 703 3088585.
Michael McCarroll, mccarroll.michael@epa.gov, 703 3470147.

assessments for the pesticides listed in the Table in Unit IV. The Agency will consider all comments received during the public comment period and make changes, as appropriate, to a draft human health and/or ecological risk
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assessment. EPA may then issue a revised risk assessment, explain any changes to the draft risk assessment, and respond to comments.
Information submission requirements.
Anyone may submit data or information
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