2018-16988. Registration Review Proposed Interim Decisions for Several Pesticides; Notice of Availability
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Start Preamble
AGENCY:
Environmental Protection Agency (EPA).
ACTION:
Notice.
SUMMARY:
This notice announces the availability of EPA's proposed interim registration review decisions and opens a 60-day public comment period on the proposed interim decisions for the chemicals listed in the Table in Unit IV of this Notice.
DATES:
Comments must be received on or before October 9, 2018.
ADDRESSES:
Submit your comments, identified by the docket identification (ID) number for the specific pesticide of interest provided in the Table in Unit IV, 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.Start Printed Page 39086
- 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.
Start Further InfoFOR 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: Dana Friedman, Pesticide Re-Evaluation Division (7508P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-0001; telephone number: (703) 347-8827; email address: friedman.dana@epa.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY 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 pesticide of interest 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 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 proposed interim decisions for all pesticides 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 the chemicals listed in the Table 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 registration review decisions for the pesticides shown in the following table, and opens a 60-day public comment period on the proposed interim decisions.
Table—Registration Review Proposed Interim Decisions Being Issued
Registration review case name and number Docket ID No. Chemical review manager and contact information Ammonia & Ammonium Sulfate, Case Numbers 7440 & 5073 EPA-HQ-OPP-2012-0684 Stephen Savage, savage.stephen@epa.gov, (703) 347-0345. Bacillus popilliae, Case 4102 EPA-HQ-OPP-2016-0043 Daniel Schoeff, schoeff.daniel@epa.gov, (703) 347-0143. Benfluralin, Case 2030 EPA-HQ-OPP-2011-0931 Michelle Nolan, nolan.michelle@epa.gov, (703) 347-0258. Chlorpropham, Case 0271 EPA-HQ-OPP-2010-0923 Marianne Mannix, mannix.marianne@epa.gov, (703) 347-0275. Citronellol (3, 7-Dimethyl-6-Octen-1-ol), Case 6086 EPA-HQ-OPP-2017-0250 Maggie Rudick, rudick.maggie@epa.gov, (703) 347-0257. Clomazone, Case 7203 EPA-HQ-OPP-2006-0113 Nicole Zinn, zinn.nicole@epa.gov, (703) 308-7076. Cytokinins, Case 4107 EPA-HQ-OPP-2012-0671 Daniel Schoeff, schoeff.daniel@epa.gov, (703) 347-0143. Dichlobenil, Case 0236 EPA-HQ-OPP-2012-0395 Linsey Walsh, walsh.linsey@epa.gov, (703) 347-8030. Diflufenzopyr & Diflufenzopyr-Sodium, Case 7246 EPA-HQ-OPP-2011-0911 Bilin Basu, basu.bilin@epa.gov, (703) 347-0455. Emamectin Benzoate, Case 7607 EPA-HQ-OPP-2011-0483 Susan Bartow, bartow.susan@epa.gov, (703) 603-0065. Fluopicolide, Case 7055 EPA-HQ-OPP-2013-0037 Khue Nguyen, nguyen.khue@epa.gov, (703) 347-0248. Fluridone, Case 7200 EPA-HQ-OPP-2009-0160 Leigh Rimmer, rimmer.leigh@epa.gov, (703) 347-0553. German cockroach pheromone, Case 6023 EPA-HQ-OPP-2017-0261 Daniel Schoeff, schoeff.daniel@epa.gov, (703) 347-0143. Start Printed Page 39087 Gibberellins, Case 4110 EPA-HQ-OPP-2012-0939 Cody Kendrick, kendrick.cody@epa.gov, (703) 347-0468. Indole-3-Butyric Acid, Case 2330 EPA-HQ-OPP-2010-0608 Seiichi Murasaki, murasaki.seiichi@epa.gov, (703) 347-0163. Indoxacarb, Case 7613 EPA-HQ-OPP-2013-0367 Moana Appleyard, appleyard.moana@epa.gov, (703) 308-8175. Methyl Eugenol, Case 6203 EPA-HQ-OPP-2016-0173 Chris Pfeifer, pfeifer.chris@epa.gov, (703) 308-0031. Methyl Isopropenyl, Case 6090 EPA-HQ-OPP-2017-0253 Alexandra Boukedes, boukedes.alexandra@epa.gov, (703) 347-0305. Naphthenate salts, Case 3099 EPA-HQ-OPP-2010-0455 Rachel Ricciardi, ricciardi.rachel@epa.gov, (703) 347-0465. Nuranone, Case 4113 EPA-HQ-OPP-2012-0126 Seiichi Murasaki, murasaki.seiichi@epa.gov, (703) 347-0163. Oxamyl, Case 0253 EPA-HQ-OPP-2010-0028 Bilin Basu, basu.bilin@epa.gov, (703) 347-0455. Prometryn, Case 0467 EPA-HQ-OPP-2013-0032 Christina Scheltema, scheltema.christina@epa.gov, (703) 308-2201. Pyriproxyfen, Case 7424 EPA-HQ-OPP-2011-0677 Khue Nguyen, nguyen.khue@epa.gov, (703) 347-0248. Quillaja extract (Quillaja Saponins), Case 6512 EPA-HQ-OPP-2017-0230 Maggie Rudick, rudick.maggie@epa.gov, (703) 347-0257. Quinoa Saponins (Extract of Chenopodium Quinoa Saponins), Case 6200 EPA-HQ-OPP-2017-0274 Daniel Schoeff, schoeff.daniel@epa.gov, (703) 347-0143. Rhamnolipid biosurfactant, Case 6085 EPA-HQ-OPP-2017-0275 Cody Kendrick, kendrick.cody@epa.gov, (703) 347-0468. Salicylic Acid and Methyl Salicylate, Case 4080 EPA-HQ-OPP-2017-0328 Maggie Rudick, rudick.maggie@epa.gov, (703) 347-0257. Trifloxystrobin, Case 7028 EPA-HQ-OPP-2013-0074 Moana Appleyard, appleyard.moana@epa.gov, (703) 308-8175. (Z)-9-tricosene (Muscalure), Case 4112 EPA-HQ-OPP-2010-0925 Alexandra Boukedes, boukedes.alexandra@epa.gov, (703) 347-0305. 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 the table in Unit IV, as well as the Agency's subsequent risk findings and consideration of possible risk mitigation measures. These proposed interim 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 the table 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 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 the pesticides included in the Table 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 registration review decision will explain the effect that any comments had on the interim decision and provide the Agency's response to significant comments.
Background on the registration review program is provided at: http://www.epa.gov/pesticide-reevaluation.
Start SignatureDated: July 16, 2018.
Yu-Ting Guilaran,
Director, Pesticide Re-Evaluation Division, Office of Pesticide Programs.
[FR Doc. 2018-16988 Filed 8-7-18; 8:45 am]
BILLING CODE 6560-50-P
Document Information
- Published:
- 08/08/2018
- Department:
- Environmental Protection Agency
- Entry Type:
- Notice
- Action:
- Notice.
- Document Number:
- 2018-16988
- Dates:
- Comments must be received on or before October 9, 2018.
- Pages:
- 39085-39087 (3 pages)
- Docket Numbers:
- EPA-HQ-OPP-2017-0750, FRL-9981-20
- PDF File:
- 2018-16988.pdf
- Supporting Documents:
- » Oxamyl Interim Registration Review Decision Case Number 0253 March 2020
- » DuPont Oxamyl Label Use Table
- » Oxamyl Proposed Interim Registration Review Decision Case Number 0253
- » Oxamyl (PC 103801): Overview of Usage and Benefits for Banana, Caneberry, Carrot, Citrus, Eggplant, Ginger Root, Mint, Peanut, Pineapple, Pome Fruit, Nonbearing Fruit, Sweet Potato and Yams, Tobacco, and Tomato
- » Oxamyl (PC 103801) Benefits Use and Usage in Dry Bulb Onion
- » Oxamyl (103801) Screening Level Usage Analysis (SLUA)
- » Oxamyl (103801)- Benefits, Use and Usage of Oxamyl in Peppers
- » Oxamyl (103801) Amended Benefits, Use and Usage in Celery
- » Oxamyl (103801) - Benefits, Use and Usage in Cucurbits
- » Oxamyl (103801) - Benefits Use and Usage in Potato