80 FR 39107 - Registration Review; Draft Human Health and Ecological Risk Assessments; Notice of Availability
ENVIRONMENTAL PROTECTION AGENCY Federal Register Volume 80, Issue 130 (July 8, 2015)
Federal Register Volume 80, Issue 130 (July 8, 2015)
| Page Range | 39107-39109 | |
| FR Document | 2015-16422 |
[Federal Register Volume 80, Number 130 (Wednesday, July 8, 2015)] [Notices] [Pages 39107-39109] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2015-16422] ----------------------------------------------------------------------- ENVIRONMENTAL PROTECTION AGENCY [EPA-HQ-OPP-2015-0386; FRL-9929-23] Registration Review; Draft Human Health and Ecological Risk Assessments; Notice of Availability AGENCY: Environmental Protection Agency (EPA). ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: This notice announces the availability of EPA's draft human health and ecological risk assessments for the registration reviews of flufenacet, flurprimidol, propoxur, and sodium acifluorfen, and opens a public comment period on these documents. In addition, this notice announces both the opening of the registration review docket for thidiazuron and the availability of the registration review draft human health and ecological risk assessments for thidiazuron. The Agency is opening a public comment period on both the Preliminary Work Plan and the draft risk assessments for thidiazuron. 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. DATES: Comments must be received on or before September 8, 2015. ADDRESSES: Submit your comments, identified by docket identification (ID) number for the specific pesticide of interest provided in Table 1 of Unit III, by one of the following methods:Federal eRulemaking Portal: 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. Mail: OPP Docket, Environmental Protection Agency Docket Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001. Hand Delivery: To make special arrangements for hand delivery or delivery of boxed information, please follow the instructions at http://www.epa.gov/dockets/contacts.html. Additional instructions on commenting or visiting the docket, along with more information about dockets generally, is available at http://www.epa.gov/dockets. FOR FURTHER INFORMATION CONTACT: For pesticide specific information contact the Chemical Review Manager listed as the contact in Table 1 of Unit III. For general questions on the registration review program, contact: Richard Dumas, Pesticide Re-Evaluation Division (7508P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; telephone number: (703) 308-8015; 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, 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 case in question, listed in Table 1 of Unit III of this notice. 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 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 [[Page 39108]] 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. Authority 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 comprehensive draft human health and ecological risk assessments, including, in some cases, a screening level endangered species assessment, for all uses of these pesticides. After reviewing comments received during the public comment period, EPA may issue revised risk assessments, explain any changes to the draft risk assessments, respond to comments, and request public input on risk mitigation before completing proposed registration review decisions for flufenacet, flurprimidol, propoxur, sodium acifluorfen, and thidiazuron. EPA is conducting its registration review of the pesticide cases listed in Table 1 of Unit III. of this notice 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 human dietary risks of concern from residues that result from the use of a pesticide in or on food. III. Registration Reviews As directed by FIFRA section 3(g), EPA is reviewing the pesticide registrations for the pesticides listed in Table 1 of this Unit to ensure that each pesticide on the list continues to satisfy the FIFRA standard for registration--that is, that these pesticides can still be used without unreasonable adverse effects on human health or the environment. Table 1--Draft Risk Assessments Being Made Available for Public Comment ------------------------------------------------------------------------ Chemical review Registration review case name manager and and No. Docket ID No. contact information ------------------------------------------------------------------------ Flufenacet, 7245................ EPA-HQ-OPP-2010-08 Margaret Hathaway, 63. [email protected], 703-305- 5076. Flurprimidol, 7000.............. EPA-HQ-OPP-2009-06 Kelly Ballard, 30. [email protected], 703-305- 8126. Propoxur, 2555.................. EPA-HQ-OPP-2009-08 Brittany Pruitt, 06. [email protected], 703-347- 0289. Sodium acifluorfen, 2605........ EPA-HQ-OPP-2010-01 Christina 35. Scheltema, [email protected], 703- 308-2201. Thidiazuron, 4092............... EPA-HQ-OPP-2015-03 Khue Nguyen, 81. [email protected], 703-347-0248. ------------------------------------------------------------------------ Flufenacet. Draft Human Health and Ecological Risk Assessments (EPA-HQ-OPP-2010-0863). Flufenacet is a pre-emergent, anilide herbicide registered for use on wheat, perennial grasses grown for seed, corn for silage, field and sweet corn, soybeans, and triticale. There are no registered residential uses of flufenacet. EPA has completed draft human health and ecological risk assessments, including a screening- level listed species assessment, for all flufenacet uses. EPA acknowledges that further refinements to the listed species assessment will be completed in future revisions and requests public comment on specific areas that will reduce the uncertainties associated with the characterization of risk to listed species identified in the current assessment. Flurprimidol. Draft Human Health and Ecological Risk Assessments (EPA-HQ-OPP-2009-0630). Flurprimidol is a plant growth regulator belonging to the pyrimidine class. It is registered for use on golf courses and ornamental turf; for landscape/woody ornamental plants and ornamental trees; and for ornamental plants grown in containers in nurseries, greenhouses, and shadehouses. EPA conducted a comprehensive human health risk assessment and did not identify any risks of concern for dietary, residential, or occupational exposures. EPA also conducted a screening level ecological risk assessment that addressed only the tree injection use of flurprimidol. Potential risks to birds, mammals, and plants were identified. All other uses of flurprimidol were addressed in a 2010 ecological risk assessment, which is posted to the registration review docket. An endangered species assessment has not been completed for flurprimidol at this time. Propoxur. Draft Human Health and Ecological Risk Assessments (EPA- HQ-OPP-2009-0806). Propoxur is a carbamate insecticide registered for use by pest control operators to kill a variety of insects including crickets, ants, cockroaches, and silverfish. It is registered for use in and around residential, industrial, institutional, and commercial facilities (including food handling establishments and food processing plants). EPA has completed draft human health and ecological risk assessments, including a screening-level listed species assessment for all propoxur uses. EPA acknowledges that [[Page 39109]] further refinements to the listed species assessment will be completed in future revisions and requests public comment on specific areas that will reduce the uncertainties associated with the characterization of risk to listed species identified in the current assessment. Sodium acifluorfen. Draft Human Health and Ecological Risk Assessments (EPA-HQ-OPP-2010-0135). Sodium acifluorfen is a post- emergent herbicide registered for use on peanuts, soybeans, strawberries, and rice. EPA has completed draft human health and ecological risk assessments for all sodium acifluorfen uses. There are no anticipated human health risks of concern. The draft ecological risk assessment indicates that there is direct risk of adverse effects to non-target organisms, including fish, birds, and mammals, and species for which these taxa serve as surrogates, and non-target terrestrial plants. The assessment did not find risks of concern for aquatic plants. Thidiazuron. Combined Docket Opening and Release of Draft Human Health and Ecological Risk Assessments (EPA-HQ-OPP-2015-0381). Thidiazuron is a plant growth regulator registered for use as a defoliant on cotton. There are no non-agricultural uses of thidiazuron. EPA has completed a combined problem formulation/preliminary ecological risk assessment and combined scoping document/preliminary human health risk assessment for thidiazuron. No human health risks of concern were identified. The ecological risk assessment indicated potential risks of concern to birds, terrestrial-phase amphibians, reptiles, and terrestrial plants. The Agency did not complete an endangered species risk assessment. Pursuant to 40 CFR 155.53(c), EPA is providing an opportunity, through this notice of availability, for interested parties to provide comments and input concerning the Agency's draft human health and ecological risk assessments for these pesticides. Such comments could address, among other things, the Agency's risk assessment methodologies and assumptions, as applied to these draft risk assessments. The Agency will consider all comments received during the public comment period and make changes, as appropriate, to the draft human health and ecological risk assessments. EPA may then issue revised risk assessments, explain any changes to the draft risk assessments, and respond to comments. In the Federal Register notice announcing the availability of any such revised risk assessments for these pesticides, if the revised risk assessments indicate risks of concern, the Agency may provide a comment period for the public to submit suggestions for mitigating the risks identified in the revised risk assessments before developing a proposed registration review decision on the affected pesticide. 1. Other related information. Additional information on the individual pesticides discussed in this notice is available through the Pesticide Registration Review Status Web page, at http://www2.epa.gov/pesticide-reevaluation/individual-pesticides-registration-review. Information on the Agency's registration review program and its implementing regulation is available at http://www2.epa.gov/pesticide-reevaluation. 2. Information submission requirements. Anyone may submit data or information in response to this document. To be considered during a pesticide's registration review, the submitted data or information must meet the following requirements: To ensure that EPA will consider data or information submitted, interested persons must submit the data or information during the comment period. The Agency may, at its discretion, consider data or information submitted at a later date. The data or information submitted must be presented in a legible and useable form. For example, an English translation must accompany any material that is not in English and a written transcript must accompany any information submitted as an audiographic or videographic record. Written material may be submitted in paper or electronic form. Submitters must clearly identify the source of any submitted data or information. Submitters may request the Agency to reconsider data or information that the Agency rejected in a previous review. However, submitters must explain why they believe the Agency should reconsider the data or information in the pesticide's registration review. As provided in 40 CFR 155.58, the registration review docket for each pesticide case will remain publicly accessible through the duration of the registration review process; that is, until all actions required in the final decision on the registration review case have been completed. Authority: 7 U.S.C. 136 et seq. Dated: June 22, 2015. Richard P. Keigwin, Jr., Director, Pesticide Re-Evaluation Division, Office of Pesticide Programs. [FR Doc. 2015-16422 Filed 7-7-15; 8:45 am] BILLING CODE 6560-50-P
![Federal Register / Vol. 80, No. 130 / Wednesday, July 8, 2015 / Notices 39107
concern to non-listed species have been Background on the registration review • Mail: OPP Docket, Environmental
identified. No risk mitigation measures program is provided at: http:// Protection Agency Docket Center (EPA/
for human health or ecological effects www2.epa.gov/pesticide-reevaluation. DC), (28221T), 1200 Pennsylvania Ave.
are included in the interim decision. Links to earlier documents related to the NW., Washington, DC 20460–0001.
Case Closure for Diclofop-methyl (PC registration review of the pesticide cases • Hand Delivery: To make special
Code: 110902, Case: 2160). Diclofop- identified in this notice are provided in arrangements for hand delivery or
methyl is an herbicide which was the Pesticide Chemical Search data base delivery of boxed information, please
labeled for use on wheat, barley, and accessible at: http://iaspub.epa.gov/ follow the instructions at http://
golf course turf. On October 23, 2014, apex/pesticides/f?p=chemicalsearch. www.epa.gov/dockets/contacts.html.
the Agency received a request for Additional instructions on
Authority: 7 U.S.C. 136 et seq.
voluntary cancellation of diclofop- commenting or visiting the docket,
methyl from the technical and end-use Dated: June 26, 2015. along with more information about
registrants; Bayer CropScience and Richard P. Keigwin, Jr., dockets generally, is available at http://
Bayer Environmental Science, Director, Pesticide Re-Evaluation Division, www.epa.gov/dockets.
respectively. EPA subsequently issued a Office of Pesticide Programs. FOR FURTHER INFORMATION CONTACT: For
Federal Register notice announcing [FR Doc. 2015–16406 Filed 7–7–15; 8:45 am] pesticide specific information contact
receipt of the request (FRL–9396–04), BILLING CODE 6560–50–P the Chemical Review Manager listed as
and allowed a 30-day period for public the contact in Table 1 of Unit III.
comment on the request. No substantive For general questions on the
comments were received, and on June ENVIRONMENTAL PROTECTION registration review program, contact:
10, 2015, EPA issued the cancellation AGENCY Richard Dumas, Pesticide Re-Evaluation
order for all remaining registrations of Division (7508P), Office of Pesticide
products containing diclofop-methyl [EPA–HQ–OPP–2015–0386; FRL–9929–23]
Programs, Environmental Protection
(FRL–9968–03), which sets out the Agency, 1200 Pennsylvania Ave. NW.,
existing stocks policy for such products. Registration Review; Draft Human
Health and Ecological Risk Washington, DC 20460–0001; telephone
With the cancellation of all remaining number: (703) 308–8015; email address:
diclofop-methyl products, the Agency is Assessments; Notice of Availability
dumas.richard@epa.gov.
announcing the closure of the AGENCY: Environmental Protection SUPPLEMENTARY INFORMATION:
registration review case for the active Agency (EPA).
ingredient. I. General Information
ACTION: Notice.
Pursuant to 40 CFR 155.57, a
A. Does this action apply to me?
registration review decision is the SUMMARY: This notice announces the
Agency’s determination whether a availability of EPA’s draft human health This action is directed to the public
pesticide meets, or does not meet, the and ecological risk assessments for the in general, and may be of interest to a
standard for registration in FIFRA. EPA registration reviews of flufenacet, wide range of stakeholders including
has considered the pesticides listed in flurprimidol, propoxur, and sodium environmental, human health, farm
the table in this unit in light of the acifluorfen, and opens a public worker, and agricultural advocates; the
FIFRA standard for registration. The comment period on these documents. In chemical industry; pesticide users; and
Interim Decision documents for these addition, this notice announces both the members of the public interested in the
pesticides in the docket describe the opening of the registration review sale, distribution, or use of pesticides.
Agency’s rationale for issuing a docket for thidiazuron and the Since others also may be interested, the
registration review interim decision for availability of the registration review Agency has not attempted to describe all
this pesticide. draft human health and ecological risk the specific entities that may be affected
In addition to an interim registration assessments for thidiazuron. The by this action. If you have any questions
review decision document, the Agency is opening a public comment regarding the applicability of this action
registration review docket for each of period on both the Preliminary Work to a particular entity, consult the
these pesticides may also include other Plan and the draft risk assessments for Chemical Review Manager for the case
relevant documents related to the thidiazuron. Through this program, EPA in question, listed in Table 1 of Unit III
registration review of the case. A is ensuring that each pesticide’s of this notice.
proposed interim registration review registration is based on current B. What should I consider as I prepare
decision was previously posted to each scientific and other knowledge, my comments for EPA?
docket and the public was invited to including its effects on human health
submit any comments or new 1. Submitting CBI. Do not submit this
and the environment. information to EPA through
information relevant to the proposal.
EPA has addressed the substantive DATES: Comments must be received on regulations.gov or email. Clearly mark
comments and information received or before September 8, 2015. the part or all of the information that
during the 60-day comment period in ADDRESSES: Submit your comments, you claim to be CBI. For CBI
the discussion for each pesticide listed identified by docket identification (ID) information in a disk or CD–ROM that
in this document. During the 60-day number for the specific pesticide of you mail to EPA, mark the outside of the
comment period, no public comments interest provided in Table 1 of Unit III, disk or CD–ROM as CBI and then
were received for any of these cases that by one of the following methods: identify electronically within the disk or
resulted in changes in the Agency’s • Federal eRulemaking Portal: http:// CD–ROM the specific information that
srobinson on DSK5SPTVN1PROD with NOTICES
interim decisions. www.regulations.gov. Follow the online is claimed as CBI. In addition to one
Pursuant to 40 CFR 155.58(c), the instructions for submitting comments. complete version of the comment that
registration review case docket for each Do not submit electronically any includes information claimed as CBI, a
pesticide discussed in this notice will information you consider to be copy of the comment that does not
remain open until all actions required in Confidential Business Information (CBI) contain the information claimed as CBI
the interim decision have been or other information whose disclosure is must be submitted for inclusion in the
completed. restricted by statute. public docket. Information so marked
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![Federal Register / Vol. 80, No. 130 / Wednesday, July 8, 2015 / Notices 39109
further refinements to the listed species of concern, the Agency may provide a Dated: June 22, 2015.
assessment will be completed in future comment period for the public to submit Richard P. Keigwin, Jr.,
revisions and requests public comment suggestions for mitigating the risks Director, Pesticide Re-Evaluation Division,
on specific areas that will reduce the identified in the revised risk Office of Pesticide Programs.
uncertainties associated with the assessments before developing a [FR Doc. 2015–16422 Filed 7–7–15; 8:45 am]
characterization of risk to listed species proposed registration review decision BILLING CODE 6560–50–P
identified in the current assessment. on the affected pesticide.
Sodium acifluorfen. Draft Human
Health and Ecological Risk Assessments 1. Other related information.
(EPA–HQ–OPP–2010–0135). Sodium Additional information on the FEDERAL COMMUNICATIONS
acifluorfen is a post-emergent herbicide individual pesticides discussed in this COMMISSION
registered for use on peanuts, soybeans, notice is available through the Pesticide
strawberries, and rice. EPA has Registration Review Status Web page, at [DA 15–679]
completed draft human health and http://www2.epa.gov/pesticide-
Media Bureau Announces Incentive
ecological risk assessments for all reevaluation/individual-pesticides-
Auction Eligible Facilities and Deadline
sodium acifluorfen uses. There are no registration-review. Information on the for Filing Pre-Auction Technical
anticipated human health risks of Agency’s registration review program Certification Form
concern. The draft ecological risk and its implementing regulation is
assessment indicates that there is direct available at http://www2.epa.gov/ AGENCY: Federal Communications
risk of adverse effects to non-target pesticide-reevaluation. Commission.
organisms, including fish, birds, and ACTION: Notice.
mammals, and species for which these 2. Information submission
taxa serve as surrogates, and non-target requirements. Anyone may submit data SUMMARY: This document announces
terrestrial plants. The assessment did or information in response to this each full power and Class A station
not find risks of concern for aquatic document. To be considered during a facility eligible for protection in the
plants. pesticide’s registration review, the repacking process and for
Thidiazuron. Combined Docket submitted data or information must relinquishment in the reverse auction
Opening and Release of Draft Human meet the following requirements: (i.e., ‘‘eligible facility’’), as well as the
Health and Ecological Risk Assessments • To ensure that EPA will consider date by which a licensee with a eligible
(EPA–HQ–OPP–2015–0381). data or information submitted, facility must file a Pre-Auction
Thidiazuron is a plant growth regulator interested persons must submit the data Technical Certification Form (FCC Form
registered for use as a defoliant on 2100, Schedule 381) (approved under
or information during the comment
cotton. There are no non-agricultural OMB control under 3060–1206). An
period. The Agency may, at its
uses of thidiazuron. EPA has completed Appendix is attached to the Public
a combined problem formulation/ discretion, consider data or information
submitted at a later date. Notice listing each eligible facility. The
preliminary ecological risk assessment Public Notice also establishes a process
and combined scoping document/ • The data or information submitted for licensees to file a Petition for Eligible
preliminary human health risk must be presented in a legible and Entity Status in order to request that a
assessment for thidiazuron. No human useable form. For example, an English facility not listed in the Appendix
health risks of concern were identified. translation must accompany any attached to the Public Notice be treated
The ecological risk assessment indicated material that is not in English and a as an eligible facility.
potential risks of concern to birds, written transcript must accompany any DATES: The deadline for filing a Pre-
terrestrial-phase amphibians, reptiles, information submitted as an
and terrestrial plants. The Agency did Auction Technical Certification Form
audiographic or videographic record. (FCC Form 2100, Schedule 381) is July
not complete an endangered species risk Written material may be submitted in
assessment. 9, 2015. The deadline for filing a
paper or electronic form. Petition for Eligible Entity Status is July
Pursuant to 40 CFR 155.53(c), EPA is
providing an opportunity, through this • Submitters must clearly identify the 9, 2015. If granted, the Bureau will
notice of availability, for interested source of any submitted data or notify the petitioner of the date by
parties to provide comments and input information. which it must file its Pre-Auction
concerning the Agency’s draft human Technical Certification Form as part of
• Submitters may request the Agency
health and ecological risk assessments its decision. Furthermore, if the
to reconsider data or information that Commission grants a petition for
for these pesticides. Such comments the Agency rejected in a previous
could address, among other things, the reconsideration of the Incentive Auction
review. However, submitters must R&O and in doing so extends
Agency’s risk assessment methodologies explain why they believe the Agency
and assumptions, as applied to these discretionary protection to a different
should reconsider the data or facility, or a facility that is not currently
draft risk assessments. The Agency will
consider all comments received during information in the pesticide’s listed in the Appendix attached to the
the public comment period and make registration review. Public Notice, the licensee must file a
changes, as appropriate, to the draft As provided in 40 CFR 155.58, the Pre-Auction Technical Certification
human health and ecological risk registration review docket for each Form for each eligible facility no later
assessments. EPA may then issue pesticide case will remain publicly than seven (7) days after release of the
srobinson on DSK5SPTVN1PROD with NOTICES
revised risk assessments, explain any accessible through the duration of the Commission’s decision or by July 9,
changes to the draft risk assessments, registration review process; that is, until 2015, whichever is later.
and respond to comments. In the all actions required in the final decision FOR FURTHER INFORMATION CONTACT:
Federal Register notice announcing the on the registration review case have Kevin Harding, Hossein Hashemzadeh,
availability of any such revised risk been completed. or Evan Morris, Video Division, Media
assessments for these pesticides, if the Bureau, Federal Communications
Authority: 7 U.S.C. 136 et seq.
revised risk assessments indicate risks Commission, (202) 418–1600.
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Document Created: 2018-02-23 09:12:52
Document Modified: 2018-02-23 09:12:52
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice. | |
| Dates | Comments must be received on or before September 8, 2015. | |
| Contact | For pesticide specific information contact the Chemical Review Manager listed as the contact in Table 1 of Unit III. | |
| FR Citation | 80 FR 39107 |
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