The nature of the residue in plants is adequately understood. However, the label for TAME 2.4 EC SprayTM does include nonfood use on indoor and outdoor ornamental and nursery plantings. A single 10-month old nursing infant consumed 2/3 of a pound (310 grams) of grapes in 1-day. Material Notes: AKROMID® T is characterized primarily by high heat resistance and the lowest moisture absorption of the manufacturer's PA grades, … Therefore, chronic exposure to fenpropathrin residues in drinking water are not expected to exceed EPA's level of concern. For more information on other … Product identifier Product form : Mixture Trade name : K KOOL-P 30% … Get contact details and address | ID: 19870596512 Some products are described in detail as examples for a given active ingredient (AI). EPA anticipates that the 1994-1996 food consumption survey will be available for use in the first quarter of calendar year 2000. 11. 2. These exposures were aggregated with the average food exposure to arrive at short-term aggregate DWLOCs. 3. SCI-GROW is an empirical model based upon actual ground water monitoring data collected for the registration of a number of pesticides that serve as benchmarks for the model. provide legal notice to the public or judicial notice to the courts. You may also send an electronic copy of your request via e-mail to: opp-docket@epa.gov. offers a preview of documents scheduled to appear in the next day's 30. regulatory information on FederalRegister.gov with the objective of The nature of the residue in animals is adequately understood. on According to the label, this product can be applied by Professional Certified Operators (PCO) only. This action does not alter the relationships or distribution of power and responsibilities established by Congress in the preemption provisions of FFDCA section 408(n)(4). There are no current registered residential uses for fenpropathrin. Nor does it require any prior consultation as specified by Executive Order 13084, entitled Consultation and Coordination with Indian Tribal Governments (63 FR 27655, May 19, 1998); special considerations as required by Executive Order 12898, entitled Federal Actions to Address Environmental Justice in Minority Populations and Low-Income Populations (59 FR 7629, February 16, 1994); or require OMB review or any Agency action under Executive Order 13045, entitled Protection of Children from Environmental Health Risks and Safety Risks (62 FR 19885, April 23, 1997). The petition requested that 40 CFR 180.466 be amended by establishing a tolerance for residues of the insecticide fenpropathrin, in or on various food commodities as follows: (1) PP7F3485 proposes the establishment of tolerances for the pome fruit crop group (crop group 11) at 5.0 parts per million (ppm); (2) PP1F3949 proposes the establishment of tolerances for grapes at 5.0 ppm and the processed product raisins at 10 ppm; for the citrus fruit crop group (crop group 10) at 2.0 ppm and the processed product citrus oil at 50.0 ppm and dried citrus pulp at 4.0 ppm. Chronic exposure and risk. This method includes cleanup procedures for oily crops and oils. publication in the future. The top countries of supplier is China, from which the percentage of fenpropathrin ec supply is 100% respectively. Pups (male/female): Developmental NOAEL = 40 ppm (3.0/3.4 mg/kg/day). Open for Comment, Economic Sanctions & Foreign Assets Control, National Oceanic and Atmospheric Administration, National Highway Traffic Safety Administration, Addressing the Threat Posed by Applications and Other Software Developed or Controlled by Chinese Companies. Document Drafting Handbook of the issuing agency. No. See Aggregate Risks and Determination of Safety for US Population in Unit III (D)(3) above. An adequate number of residue field trials reflecting the proposed use rates were submitted to EPA to demonstrate that tolerances for pome fruit (crop group 11) and grapes at 5.0 ppm; head and stem Brassica (crop group 5A) at 3.0 ppm; citrus fruit (crop group 10) at 2.0 ppm; melons (crop group 9A) at 0.5 ppm; processed products citrus oil at 75 ppm, raisins at 10 ppm, and dried citrus pulp at 4.0 ppm will not be exceeded when fenpropathrin products labeled for these uses are used as directed. A copy of the information that does not contain CBI must be submitted for inclusion in the public record. For further discussion of the regulatory requirements of section 408 and a complete description of the risk assessment process, see the final rule on Bifenthrin Pesticide Tolerances (62 FR 62961, November 26, 1997) (FRL-5754-7). (ii). Short- and intermediate-term toxicity. You may obtain electronic copies of this document, and certain other related documents that might be available electronically, from the EPA Internet Home Page at http://www.epa.gov/​. Based on the 1989-1992 data base, the most highly exposed subgroup (children 1-6 years) utilized 9% of the cPAD. The documents posted on this site are XML renditions of published Federal 01/08/2021, 307 EPA has also considered available information concerning the variability of the sensitivities of major identifiable subgroups of consumers, including infants and children. Mortality was highest during the final quarter of the study, but the incidence was similar in all dosed and control groups. The EPA procedural regulations which govern the submission of objections and requests for hearings appear in 40 CFR part 178. s. No. The nature of the Start Printed Page 11236toxic effects caused by fenpropathrin are discussed in this unit. Using the exposure assumptions described in this unit, EPA has concluded that aggregate exposure to fenpropathrin from food will utilize 5% of the cPAD for infants and 9% for children. 3. The Agency used PCT information as follows: The Agency believes that the three conditions, discussed in section 408 (b)(2)(F) in this unit concerning the Agency's responsibilities in assessing chronic dietary risk findings, have been met. 01/08/2021, 390 GENEEC can substantially overestimate (by a ≥3-fold factor) true pesticide concentrations in drinking water. Consistent with section 408(b)(2)(D), EPA has reviewed the available scientific data and other relevant information in support of this action. PEEK 30% … Your objection must specify the specific provisions in the regulation that you object to, and the grounds for the objections (40 CFR 178.25). 01/08/2021, 40 Packaging: Available in all standards pack sizes or as per customer’s specifications. Tolfenpyrad EC Tolfenpyrad EC 33.3 Chlorpyrifos Lorsban 89.0 Pyrifluquinazon Pyrifluquinazon 28.3 Acephate Orthene 87.5 Kaolin Clay Surround 23.1 Fenpropathrin Danitol 78.3 Diazinon Diazinon 20.4 Permethrin Permethrin 77.1 Phosmet Imidan 20.0 Azinphosmethyl Guthion 71.3 Acetamiprid Assail 18.8 … Travel Carry Ons Spinners Garment Bags Duffels Hardsides Business Everyday & Leisure Last Chance What are you looking for? Therefore, an assessment for residential handlers is not required. Margins of safety are incorporated into EPA risk assessments either directly through use of a margin of exposure (MOE) analysis or through using uncertainty (safety) factors in calculating a dose level that poses no appreciable risk to humans. Acute risk. As no indication of carcinogenicity was seen in rats or mice, fenpropathrin was classified as a group E chemical. This final rule establishes tolerances under FFDCA section 408(d) in response to a petition submitted to the Agency. ✓Thank youThanks for sharing your contact infoWe will get back shortly, We will contact you soon for better understanding of your product requirement & specification, © Redox Industries Limited. Makarba, Ahmedabad, Gujarat At that time, EPA may require further testing of this active ingredient and end use products for further endocrine disrupter effects. The Dietary Exposure Evaluation Model (DEEM) acute analysis provides an estimate of the distribution of single-day exposures for the overall U.S. population and certain subgroups. 59639-35) and TAME 2.4 EC Spray (EPA Reg. on FederalRegister.gov It is very useful for preventing plants from diseases and is widely appreciated by customers across the globe. This feature is not available for this document. Rats received 14 daily oral low-doses of 2.5 mg/kg/day of unlabeled fenpropathrin followed by a 15th dose of either the alcohol or acid radiolabeled fenpropathrin. Willowood, UPL, Coromandel, Agro Life Science, Insecticides India, Best Crop Science and many other companies got approvals in different categories. VIII. 2. 21 U.S.C. The registrant submitted the results of confined and rotational crop studies. EPA has evaluated the available toxicity data and considered its validity, completeness, and reliability as well as the relationship of the results of the studies to human risk. of this preamble. Glucoside conjugates of 3-phenoxy-benzyl alcohol and 3-phenoxybenzoic acid, administered orally to rats, were absorbed as the corresponding aglycones following cleavage of the glycoside linkage in the gut. The systemic NOAEL (male) is 450 ppm (17.06 mg/kg/day). This regulation is effective March 2, 2000. Under section 408(g) of the FFDCA, as amended by the FQPA, any person may file an objection to any aspect of this regulation and may also request a hearing on those objections. The exposure at the 99.5th percentile places less weight on the extreme value in the food consumption survey. Pendimethalin 30% EC. This notice included a summary of the petition prepared by Valent USA Company, the registrant. The NOAEL was 2.5 mg/kg/day to which an uncertainty factor of 100 was applied. 1. Dose:For actual doses please check leaflet/label enclosed with pack … The exposure of all subgroups at the 99.9th percentile is below 100% aPAD with two exceptions: nursing infants and children 1-6 years (164% and 107%, respectively). These studies are adequate to support the proposed use of fenpropathrin on head and stem Brassica and melons. It is a selective herbicide for the control of susceptible annual grasses, sedges and broad-leaved weeds in Soybean crop. Read about company. Our clients can avail the product from us at very reasonable rates and within the specified time period. A Rule by the Environmental Protection Agency on 03/02/2000. There are no uses registered for professional indoor pest control, termite prevention, homeowner use, or turf application. You may be affected by this action if you are an agricultural producer, food manufacturer, or pesticide manufacturer. For all infant/children population subgroups the DWLOCs exceeded the maximum EEC. ii. 2. If the GENEEC model value is > 3 times the chronic DWLOC, the pesticide is considered to have passed the screen and no further assessment is needed. 3. Maternal NOAEL is 4 mg/kg/day; maternal LEL is 12 mg/kg/day based on grooming, anorexia, flicking of the forepaws; developmental NOAEL is > 36 mg/kg/day (HDT). The Agency has determined that there is no evidence of carcinogenicity in studies in either the mouse or rat. EPA feels that this action is justified for the following reasons: (1) There were only 4 nursing infants in the 1989-1992 survey who ate grapes (the one data point will therefore exert an inordinate amount of influence on the results of the analysis, particularly at the 99.9th percentile); (2) for most population subgroups the aPAD values given by the two consumption surveys were comparable; (3) field trial data were used in the analysis which makes the analysis more conservative than if monitoring data had been available; (4) although the analysis is refined there is still room for further refinement—100% PCT was assumed for the following crops: grapes, pome fruits, citrus, head and stem Brassica, and melons (based on PCT values for Start Printed Page 11238registered uses, the PCT for proposed uses will probably be well below 100% once the uses are granted); and (5) although acute exposure to fenpropathrin resulting from residues present in animal commodities is refined, there is room for further refinement here also. electronic version on GPO’s govinfo.gov. Oral LD50 in the rat is 54.0 milligram/kilogram (mg/kg) for males and 48.5 (mg/kg) for females—Toxicity Category I; dermal LD50 is 1,600 mg/kg for males and 870 mg/kg for females—Category II; acute inhalation (unable to generate sufficient test article vapor or aerosol to elicit toxicity)—Category IV; primary eye irritation (no corneal involvement, mild iris and conjunctival irritation)—Category III; and primary dermal irritation (no irritation)—Category IV. 3. … Determination of safety. Kilweed 38E. P103 Read … iv. The public version of the official record does not include any information claimed as CBI. Risk assessments were conducted by EPA to assess dietary exposures from fenpropathrin as follows: i. Because of the aberrant data point, the analysis was run using the 1994-1996 food consumption survey. -for TI vs TIM Paraquat Dichloride 7.50% +Glyphosate 30% … The 1989-1992 food consumption survey was used. Chronic exposure and risk. Market area . CAS number: 134-62-3 . establishing the XML-based Federal Register as an ACFR-sanctioned 01/08/2021, 860 of this preamble. New Documents No other indications of toxicity or carcinogenicity were seen. Fenazaquin 10 EC 1.5 ml Yellow Magister 35. Residues are extracted with acetone/hexane, cleaned up with silica gel and C18 Sep Pak chromatography and detection is by gas chromatography. EPA anticipates that the 1994-1996 food consumption survey will be available for use in the first quarter of calendar year 2000. EPA has used drinking water numbers based on Generic Estimated Environmental Concentration (GENEEC) and Screening Concentration in Ground Water (SCI-GROW) modeling. corresponding official PDF file on govinfo.gov. for better understanding how a document is structured but 1. 346a as amended by the Food Quality Protection Act of 1996 (FQPA) (Public Law 104-170) announcing the filing of pesticide petitions (PP 7F3485, 6F4648, 1F3949) for a tolerance by Valent USA Company, 1333 North California Boulevard, Suite 600, Walnut Creek, CA 94596-8025. In a 21-day dermal toxicity study, rabbits were dosed 5 days/week for 3 weeks on abraded or unabraded skin at doses of 0, 500, 1,200, or 3,000 mg/kg/day. 100ml-5Ltrs. In a chronic feeding/carcinogenicity study, mice were dosed at 0, 40, 150, or 600 ppm in the feed (0, 3.9, 13.7, or 56.0 mg/kg/day in males, and 0, 4.2, 16.2, or 65.2 mg/kg/day in females). In a developmental toxicity study in rats, pregnant female rats were dosed by gavage on gestation days 6-15 at 0 (corn oil control), 0.4, 1.5, 2.0, 3.0, 6.0, or 10.0 mg/kg/day. The major elimination products in the feces included the parent chemical (13-34% of the administered dose) and four metabolites. documents in the last year, by the Pension Benefit Guaranty Corporation 100ml-5Ltrs. * * * ” The Agency is currently working with interested stakeholders, including other government agencies, public interest groups, industry and research scientists in developing a screening and testing program and a priority setting scheme to implement this program. B. The organs in which metabolites of the synthetic pyrethroids are found (i.e., liver and kidney) are minor human food consumption items. 338 with extreme priority to meet the expansion of veterinary and the agricultural requirements for local, national and international markets. These tools are designed to help you understand the official document As required by section 408(b)(2)(E), EPA will issue a data call-in for information relating to anticipated residues to be submitted no later than 5 years from the date of issuance of this tolerance. Our organization is instrumental in offering a wide array of Herbicides, which is non toxic and acts as pest repellent and pest reproduction controller. These short term MOEs are above 100 and do not exceed EPA's level of concern. P102 Keep out of reach of children. The systemic LEL (female) is 450 ppm (19.45 mg/kg/day) based on increased mortality and body tremors. Counts are subject to sampling, reprocessing and revision (up or down) throughout the day. documents in the last year, 25 The major urinary metabolites of the acid-labeled fenpropathrin were TMPA-glucuronic acid and TMPA-CH2 OH (11-26% and 6-10% of the administered dose, respectively). A. are not part of the published document itself. If you would like to request a waiver of the tolerance objection fees, you must mail your request for such a waiver to: James Hollins, Information Resources and Services Division (7502C), Office of Pesticide Programs, Environmental Protection Agency, Ariel Rios Building, 1200 Pennsylvania Ave., NW., Washington, DC 20460. Therefore, the tolerance is established for residues of fenpropathrin in pome fruit (crop group 11) and grapes at 5.0 ppm; head and stem Brassica (crop group 5A) at 3.0 ppm; citrus fruit (crop group 10) at 2.0 ppm; melons (crop group 9A) at 0.5 ppm; and in the processed products citrus oil at 75 ppm, raisins at 10 ppm, and dried citrus pulp at 4.0 ppm. Therefore it is current EPA policy to use the 1989-1992 survey. The symbol OG indicates a pesticide that has been listed by the Organic Materials Review Institute (OMRI) as approved for use in organic production.. No clinical signs were seen in any rats. Rotational crop studies are not required for grapes, citrus, and pome fruit. There were no comments received in response to the notice of filing. 3. Therefore, chronic aggregate risk does not exceed EPA's level of concern. Potentially affected categories and entities may include, but are not limited to: This listing is not intended to be exhaustive, but rather provides a guide for readers regarding entities likely to be affected by this action. on The Agency used its GENEEC screening model and environmental fate data to determine the EECs for fenpropathrin in surface water. Is expected uncertainty factor of three when determining whether or not a “ major rule ” as defined by U.S.C..., temperature sensor to pesticide residues customers end drinking water of estimates derived. 2 meters deep edge-of-the-field farm pond which receives pesticide runoff from a treated hectare. Observance of tremors in all dosed fenpropathrin 30% ec trade name control groups listed in the version! 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