80 FR 57166 - Pesticides; Revised Fee Schedule for Registration Applications
ENVIRONMENTAL PROTECTION AGENCY Federal Register Volume 80, Issue 183 (September 22, 2015)
Federal Register Volume 80, Issue 183 (September 22, 2015)
| Page Range | 57166-57178 | |
| FR Document | 2015-24064 |
[Federal Register Volume 80, Number 183 (Tuesday, September 22, 2015)] [Notices] [Pages 57166-57178] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2015-24064] ======================================================================= ----------------------------------------------------------------------- ENVIRONMENTAL PROTECTION AGENCY [EPA-HQ-OPP-2015-0614; FRL-9933-75] Pesticides; Revised Fee Schedule for Registration Applications AGENCY: Environmental Protection Agency (EPA). ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: EPA is publishing a revised list of pesticide registration service fees applicable to specified pesticide applications and tolerance actions. Under the Pesticide Registration Improvement Extension Act, the registration service fees for covered pesticide registration applications received on or after October 1, 2015, increase by 5% rounding up to the nearest dollar from the fees published for fiscal year 2015. The new fees for FY'2016 become effective on October 1, 2015. FOR FURTHER INFORMATION CONTACT: Peter Caulkins (7501P), Immediate Office, Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; telephone number: (703) 305-6550; fax number: (703) 308-4776; email address: [email protected]. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? You may be potentially affected by this action if you register pesticide products under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). Potentially affected entities may include, but are not limited to:Agricultural pesticide manufacturers (NAICS code 32532). Antimicrobial pesticide manufacturers (NAICS code 32561). Antifoulant pesticide manufacturers (NAICS code 32551). Wood preservative manufacturers (NAICS code 32519). This listing is not intended to be exhaustive, but rather provides a guide for readers regarding entities likely to be affected by this action. Other types of entities not listed in this unit could also be affected. The North American Industrial Classification System (NAICS) codes have been provided to assist you and others in determining whether this action might apply to certain entities. To determine whether you or your business may be affected by this action, you should carefully examine the applicability provisions in the notice and in FIFRA section 33. If you have any questions regarding the applicability of this action to a particular entity, consult the person listed under FOR FURTHER INFORMATION CONTACT. B. How can I get copies of this document and other related information? The docket for this action, identified by docket identification (ID) number EPA-HQ-OPP-2015-0614, is available at http://www.regulations.gov or at the Office of Pesticide Programs Regulatory Public Docket (OPP Docket) in the Environmental Protection Agency Docket Center (EPA/DC), EPA West Bldg., Rm. 3334, 1301 Constitution Ave. NW., Washington, DC 20460-0001. The Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number for the Public Reading Room is (202) 566-1744, and the telephone number for the OPP Docket is (703) 305- 5805. Please review the visitor instructions and additional [[Page 57167]] information about the docket available at http://www.epa.gov/dockets. II. Background A. What action is the agency taking? The Pesticide Registration Improvement Act of 2003 established a new section 33 of FIFRA creating a registration service fee system for certain types of pesticide applications, establishment of tolerances, and certain other regulatory decisions under FIFRA and the Federal Food, Drug, and Cosmetic Act (FFDCA). Section 33 also created a schedule of decision review times for applications covered by the service fee system. The Agency began administering the registration service fee system for covered applications received on or after March 23, 2004. On September 28, 2012, the Pesticide Registration Improvement Extension Act was signed by the President, revising, among other things, FIFRA section 33. The new law reauthorized the service fee system through fiscal year 2017 and established fees and review times for applications received during fiscal years 2013 through 2017. As required by section 33(b)(6)(A) of FIFRA, the registration service fees for covered pesticide registration applications received on or after October 1, 2015, increase by 5% rounding up to the nearest dollar from the fees published in the September 26, 2013, ``Pesticides: Fee Schedule for Registration Applications,'' FRN Vol. 78. No. 187 pp. 59347-59359. B. What is the agency's authority for taking this action? The publication of this fee schedule is required by section 33(b)(6)(C) of FIFRA as amended. III. Elements of the Fee Schedule This unit explains how to read the fee schedule tables, and includes a key to terminology published with the table. A. The Pesticide Registration Improvement Extension Act Fee Schedule The fee schedule published in the Pesticide Registration Improvement Extension Act of September 28, 2012, identifies the registration service fees and decision times and is organized according to the organizational units of the Office of Pesticide Programs (OPP) within EPA. Thereafter, the categories within the organizational unit sections of the table are further categorized according to the type of application being submitted, the use patterns involved, or, in some cases, upon the type of pesticide that is the subject of the application. The fee categories differ by Division. Not all application types are covered by, or subject to, the fee system. B. Fee Schedule and Decision Review Times In today's notice, EPA has retained the format of the tables included in the Pesticide Registration Improvement Extension Act of September 28, 2012. The schedules are presented as 19 tables, organized by OPP Division and by type of application or pesticide subject to the fee. Unit IV presents fee tables for the Registration Division (RD) (6 tables), the Antimicrobials Division (AD) (4 tables), the Biopesticides and Pollution Prevention Division (BPPD) (7 tables), Inert Ingredients (1 table), Miscellaneous (1 table). C. How To Read the Tables 1. Each table consists of the following columns: The column titled ``EPA No.'' assigns an EPA identifier to each fee category. There are 189 categories spread across the 3 Divisions. There are 63 RD categories, 39 AD categories, 69 BPPD categories, 10 inert categories, and 8 miscellaneous categories. For tracking purposes, OPP has assigned a 3-digit identifier to each category, beginning with RD categories, followed by AD, BPPD, inert and miscellaneous categories. The categories are prefaced with a letter designation indicating which Division of OPP is responsible for applications in that category (R=Registration Division, A=Antimicrobials Division, B=Biopesticides and Pollution Prevention Division, I=inert ingredients, M=miscellaneous). The column titled ``CR No.'' cross-references the current Congressional Record category number for convenience. However, EPA will be using the categories as numbered in the ``EPA No.'' column in its tracking systems. The column titled ``Action'' ' describes what registration actions are covered by each category. The column titled ``Decision Time'' lists the decision times in months for each type of action. The column titled ``FY' 2016/17 Registration Service Fee ($)'' lists the registration service fee for the action for fiscal year 2016 (October 1, 2015 through September 30, 2016) and fiscal year 2017 (October 1, 2016 through September 30, 2017). Footnote text has been removed to save on Federal Register costs but remains unchanged from what was published in FY' 2013. The tables and footnote text will be available in full after October 1, 2015 at http://www.epa.gov/pesticides/regulating/fees/tool/category-table.html. 2. The following acronyms are used in some of the tables: DART--Dose Adequacy Response Team. DNT--Developmental Neurotoxicity. HSRB--Human Studies Review Board. GW/SW--Ground Water/Surface Water. PHI-Pre--Harvest Interval. PPE--Personal Protective Equipment. REI--Restricted Entry Interval. SAP--FIFRA Scientific Advisory Panel. IV. PRIA Fee Schedule Tables--Effective October 1, 2015 A. Registration Division (RD) The Registration Division of OPP is responsible for the processing of pesticide applications and associated tolerance petitions for pesticides that are termed ``conventional chemicals,'' excluding pesticides intended for antimicrobial uses. The term ``conventional chemical'' is a term of art that is intended to distinguish synthetic chemicals from those that are of naturally occurring or non-synthetic origin, synthetic chemicals that are identical to naturally occurring chemicals and microbial pesticides. Tables 1 through 6 cover RD actions. Table 1--Registration Division--New Active Ingredients ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- R010............................. 1 New Active Ingredient, Food 24 627,568 use. R020............................. 2 New Active Ingredient, Food 18 627,568 use; reduced risk. [[Page 57168]] R040............................. 3 New Active Ingredient, Food 18 462,502 use; Experimental Use Permit application; establish temporary tolerance; submitted before application for registration; credit 45% of fee toward new active ingredient application that follows. R060............................. 4 New Active Ingredient, Non- 21 436,004 food use; outdoor. R070............................. 5 New Active Ingredient, Non- 16 436,004 food use; outdoor; reduced risk. R090............................. 6 New Active Ingredient, Non- 16 323,690 food use; outdoor; Experimental Use Permit application; submitted before application for registration; credit 45% of fee toward new active ingredient application that follows. R110............................. 7 New Active Ingredient, Non- 20 242,495 food use; indoor. R120............................. 8 New Active Ingredient, Non- 14 242,495 food use; indoor; reduced risk. R121............................. 9 New Active Ingredient, Non- 18 182,327 food use; indoor; Experimental Use Permit application; submitted before application for registration; credit 45% of fee toward new active ingredient application that follows. R122............................. 10 Enriched isomer(s) of 18 317,128 registered mixed-isomer active ingredient. R123............................. 11 New Active Ingredient, Seed 18 471,861 treatment only; includes agricultural and non- agricultural seeds; residues not expected in raw agricultural commodities. R125............................. 12 New Active Ingredient, Seed 16 323,690 treatment; Experimental Use Permit application; submitted before application for registration; credit 45% of fee toward new active ingredient application that follows. ---------------------------------------------------------------------------------------------------------------- Table 2--Registration Division--New Uses ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- R130............................. 13 First food use; indoor; food/ 21 191,444 food handling. R140............................. 14 Additional food use; Indoor; 15 44,672 food/food handling. R150............................. 15 First food use............... 21 264,253 R160............................. 16 First food use; reduced risk. 16 264,253 R170............................. 17 Additional food use.......... 15 66,124 R175............................. 18 Additional food uses covered 10 66,124 within a crop group resulting from the conversion of existing approved crop group(s) to one or more revised crop groups.. R180............................. 19 Additional food use; reduced 10 66,124 risk. R190............................. 20 Additional food uses; 6 or 15 396,742 more submitted in one application. R200............................. 21 Additional food use; 6 or 10 396,742 more submitted in one application; reduced risk. R210............................. 22 Additional food use; 12 48,986 Experimental Use Permit application; establish temporary tolerance; no credit toward new use registration. R220............................. 23 Additional food use; 6 19,838 Experimental Use Permit application; crop destruct basis; no credit toward new use registration. R230............................. 24 Additional use; non-food; 15 26,427 outdoor. R240............................. 25 Additional use; non-food; 10 26,427 outdoor; reduced risk. R250............................. 26 Additional use; non-food; 6 19,838 outdoor; Experimental Use Permit application; no credit toward new use registration. R251............................. 27 Experimental Use Permit 8 19,838 application which requires no changes to the tolerance(s); non-crop destruct basis. R260............................. 28 New use; non-food; indoor.... 12 12,764 R270............................. 29 New use; non-food; indoor; 9 12,764 reduced risk. R271............................. 30 New use; non-food; indoor; 6 9,725 Experimental Use Permit application; no credit toward new use registration. R273............................. 31 Additional use; seed 12 50,445 treatment; limited uptake into raw agricultural commodities; includes crops with established tolerances (e.g., for soil or foliar application); includes food and/or non-food uses. R274............................. 32 Additional uses; seed 12 302,663 treatment only; 6 or more submitted in one application; limited uptake into raw agricultural commodities; includes crops with established tolerances (e.g., for soil or foliar application); includes food and/or non-food uses. ---------------------------------------------------------------------------------------------------------------- Table 3--Registration Division--Import and Other Tolerances ---------------------------------------------------------------------------------------------------------------- FY '16/17-- Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- R280............................. 33 Establish import tolerance; 21 319,072 new active ingredient or first food use. [[Page 57169]] R290............................. 34 Establish Import tolerance; 15 63,816 Additional new food use. R291............................. 35 Establish import tolerances; 15 382,886 additional food uses; 6 or more crops submitted in one petition. R292............................. 36 Amend an established 11 45,341 tolerance (e.g., decrease or increase); domestic or import; applicant-initiated. R293............................. 37 Establish tolerance(s) for 12 53,483 inadvertent residues in one crop; applicant-initiated. R294............................. 38 Establish tolerances for 12 320,894 inadvertent residues; 6 or more crops submitted in one application; applicant- initiated. R295............................. 39 Establish tolerance(s) for 15 66,124 residues in one rotational crop in response to a specific rotational crop application; applicant- initiated. R296............................. 40 Establish tolerances for 15 396,742 residues in rotational crops in response to a specific rotational crop petition; 6 or more crops submitted in one application; applicant- initiated. R297............................. 41 Amend 6 or more established 11 272,037 tolerances (e.g., decrease or increase) in one petition; domestic or import; applicant-initiated. R298............................. 42 Amend an established 13 58,565 tolerance (e.g., decrease or increase); domestic or import; submission of amended labels (requiring science review) in addition to those associated with the amended tolerance; applicant- initiated). R299............................. 43 Amend 6 or more established 13 285,261 tolerances (e.g., decrease or increase); domestic or import; submission of amended labels (requiring science review) in addition to those associated with the amended tolerance; applicant- initiated). ---------------------------------------------------------------------------------------------------------------- Table 4--Registration Division--New Products ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- R300............................. 44 New product; or similar 4 1,582 combination product (already registered) to an identical or substantially similar in composition and use to a registered product; registered source of active ingredient; no data review on acute toxicity, efficacy or CRP--only product chemistry data; cite-all data citation, or selective data citation where applicant owns all required data, or applicant submits specific authorization letter from data owner Category also includes 100% re-package of registered end- use or manufacturing-use product that requires no data submission nor data matrix. R301............................. 45 New product; or similar 4 1,897 combination product (already registered) to an identical or substantially similar in composition and use to a registered product; registered source of active ingredient; selective data citation only for data on product chemistry and/or acute toxicity and/or public health pest efficacy, where applicant does not own all required data and does not have a specific authorization letter from data owner. R310............................. 46 New end-use or manufacturing- 7 5,301 use product with registered source(s) of active ingredient(s); includes products containing two or more registered active ingredients previously combined in other registered products; requires review of data package within RD only; includes data and/or waivers of data for only: Product chemistry and/or acute toxicity and/or public health pest efficacy and/or child resistant packaging. R314............................. 47 New end use product 8 6,626 containing two or more registered active ingredients never before registered as this combination in a formulated product; new product label is identical or substantially similar to the labels of currently registered products which separately contain the respective component active ingredients; requires review of data package within RD only; includes data and/or waivers of data for only: Product chemistry and/or acute toxicity and/or public health pest efficacy and/or child resistant packaging. R315............................. 48 New end-use non-food animal 9 8,820 product with submission of two or more target animal safety studies; includes data and/or waivers of data for only: Product chemistry and/or acute toxicity and/or public health pest efficacy and/or animal safety studies and/or child resistant packaging. R320............................. 49 New product; new physical 12 13,226 form; requires data review in science divisions. R331............................. 50 New product; repack of 3 2,530 identical registered end-use product as a manufacturing- use product; same registered uses only. [[Page 57170]] R332............................. 51 New manufacturing-use 24 283,215 product; registered active ingredient; unregistered source of active ingredient; submission of completely new generic data package; registered uses only; requires review in RD and science divisions. R333............................. 52 New product; MUP or End use 10 19,838 product with unregistered source of active ingredient; requires science data review; new physical form; etc Cite-all or selective data citation where applicant owns all required data. R334............................. 53 New product; MUP or End use 11 19,838 product with unregistered source of the active ingredient; requires science data review; new physical form; etc Selective data citation. ---------------------------------------------------------------------------------------------------------------- Table 5--Registration Division--Amendments to Registration ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- R340............................. 54 Amendment requiring data 4 3,988 review within RD (e.g., changes to precautionary label statements). R345............................. 55 Amending non-food animal 7 8,820 product that includes submission of target animal safety data; previously registered. R350............................. 56 Amendment requiring data 9 13,226 review in science divisions (e.g., changes to REI, or PPE, or PHI, or use rate, or number of applications; or add aerial application; or modify GW/SW advisory statement). R351............................. 57 Amendment adding a new 8 13,226 unregistered source of active ingredient. R352............................. 58 Amendment adding already 8 13,226 approved uses; selective method of support; does not apply if the applicant owns all cited data. R371............................. 59 Amendment to Experimental Use 6 10,090 Permit; (does not include extending a permit's time period). ---------------------------------------------------------------------------------------------------------------- Table 6--Registration Division--Other Actions ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (Months) ($) ---------------------------------------------------------------------------------------------------------------- R124............................. 60 Conditional Ruling on 6 2,530 Preapplication Study Waivers; applicant-initiated. R272............................. 61 Review of Study Protocol 3 2,530 applicant-initiated; excludes DART, pre- registration conference, Rapid Response review, DNT protocol review, protocol needing HSRB review. R275............................. 62 Rebuttal of agency reviewed 3 2,530 protocol, applicant initiated. R370............................. 63 Cancer reassessment; 18 198,250 applicant-initiated. ---------------------------------------------------------------------------------------------------------------- B. Antimicrobials Division (AD) The Antimicrobials Division of OPP is responsible for the processing of pesticide applications and associated tolerances for conventional chemicals intended for antimicrobial uses, that is, uses that are defined under FIFRA section 2 (mm)(1)(A), including products for use against bacteria, protozoa, non-agricultural fungi, and viruses. AD is also responsible for a selected set of conventional chemicals intended for other uses, including most wood preservatives and antifoulants. Tables 7 through 10 cover AD actions. Table 7--Antimicrobials Division--New Active Ingredients ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (Months) ($) ---------------------------------------------------------------------------------------------------------------- A380............................. 64 New Active Ingredient Food 24 114,867 use, establish tolerance exemption. A390............................. 65 New Active Ingredient Food 24 191,444 use, establish tolerance. A400............................. 66 New Active Ingredient, Non- 18 95,724 food use, outdoor, FIFRA Sec. 2 (mm) uses. A410............................. 67 New Active Ingredient Non- 21 191,444 food use, outdoor, uses other than FIFRA Sec. 2(mm). A420............................. 68 New Active Ingredient Non- 18 63,816 food use, indoor, FIFRA Sec. 2(mm) uses. [[Page 57171]] A430............................. 69 New Active Ingredient, Non- 20 95,724 Food Use Indoor, uses other than FIFRA Sec. 2(mm) uses. A431............................. 70 New Active Ingredient, Non- 12 66,854 food use; indoor; low-risk; low-toxicity food grade active ingredient(s); efficacy testing for public health claims required under GLP and following DIS/TSS or AD-approved study protocol. ---------------------------------------------------------------------------------------------------------------- Table 8--Antimicrobials Division--New Uses ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (Months) ($) ---------------------------------------------------------------------------------------------------------------- A440............................. 71 New Use, First Food Use, 21 31,910 establish tolerance exemption. A450............................. 72 New use, First food use, 21 95,724 establish tolerance. A460............................. 73 New use, additional food use; 15 12,764 establish tolerance exemption. A470............................. 74 New use, additional food use, 15 31,910 establish tolerance. A471............................. 75 Additional food uses; 15 191,452 establish tolerances; 6 or more submitted in one application. A480............................. 76 New use, Additional use, non- 9 19,146 food, outdoor; FIFRA Sec. 2(mm) uses. A481............................. 77 Additional non-food outdoor 9 114,870 uses; FIFRA Sec. 2(mm) uses; 6 or more submitted in one application. A490............................. 78 New use, additional use, non- 15 31,910 food, outdoor, uses other than FIFRA Sec. 2(mm). A491............................. 79 Additional non-food; outdoor; 15 191,452 uses other than FIFRA Sec. 2(mm); 6 or more submitted in one application. A500............................. 80 New use, additional use, non- 9 12,764 food, indoor FIFRA Sec. 2(mm) uses. A501............................. 81 Additional non-food; indoor; 9 76,583 FIFRA Sec. 2(mm) uses; 6 or more submitted in one application. A510............................. 82 New use, additional use, non- 12 12,764 food, indoor, other than FIFRA Sec. 2(mm). A511............................. 83 Additional non-food; indoor; 12 76,583 uses other than FIFRA Sec. 2(mm); 6 or more submitted in one application. ---------------------------------------------------------------------------------------------------------------- Table 9--Antimicrobials Division-New Products and Amendments ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (Months) ($) ---------------------------------------------------------------------------------------------------------------- A530............................. 84 New product, identical or 4 1,278 substantially similar in composition and use to a registered product; no data review or only product chemistry data; cite all data citation or selective data citation where applicant owns all required data; or applicant submits specific authorization letter from data owner. Category also includes 100% re-package of registered end- use or manufacturing use product that requires no data submission nor data matrix. A531............................. 85 New product; identical or 4 1,824 substantially similar in composition and use to a registered product; registered source of active ingredient: Selective data citation only for data on product chemistry and/or acute toxicity and/or public health pest efficacy, where applicant does not own all required data and does not have a specific authorization letter from data owner. A532............................. 86 New product; identical or 5 5,107 substantially similar in composition and use to a registered product; registered active ingredient; unregistered source of active ingredient; cite-all data citation except for product chemistry; product chemistry data submitted. A540............................. 87 New end use product; FIFRA 5 5,107 Sec. 2(mm) uses only (2) (3). A550............................. 88 New end-use product; uses 7 5,107 other than FIFRA Sec. 2(mm); non-FQPA product. A560............................. 89 New manufacturing use 12 19,146 product; registered active ingredient; selective data citation. A570............................. 90 Label amendment requiring 4 3,831 data review. A572............................. 91 New Product or amendment 9 13,226 requiring data review for risk assessment by Science Branch (e.g., changes to REI, or PPE, or use rate). ---------------------------------------------------------------------------------------------------------------- [[Page 57172]] Table 10--Antimicrobials Division--Experimental Use Permits and Other Type of Actions ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (Months) ($) ---------------------------------------------------------------------------------------------------------------- A520............................. 92 Experimental Use Permit 9 6,383 application, non-food use. A521............................. 93 Review of public health 3 2,482 efficacy study protocol within AD, per AD Internal Guidance for the Efficacy Protocol Review Process; Code will also include review of public health efficacy study protocol and data review for devices making pesticidal claims; applicant-initiated; Tier 1. A522............................. 94 Review of public health 12 12,156 efficacy study protocol outside AD by members of AD Efficacy Protocol Review Expert Panel; Code will also include review of public health efficacy study protocol and data review for devices making pesticidal claims; applicant-initiated; Tier 2.. A523............................. 101 Review of protocol other than 9 12,156 a public health efficacy study (i.e., Toxicology or Exposure Protocols). A524............................. 95 New Active Ingredient, 18 153,156 Experimental Use Permit application; Food Use Requires Tolerance. Credit 45% of fee toward new active ingredient application that follows. A525............................. 96 New Active Ingredient, 18 92,163 Experimental Use Permit application; Food Use Requires Tolerance Exemption. Credit 45% of fee toward new active ingredient application that follows. A526............................. 97 New Active Ingredient, 15 95,724 Experimental Use Permit application; Non-Food, Outdoor Use. Credit 45% of fee toward new active ingredient application that follows. A527............................. 98 New Active Ingredient, 15 63,945 Experimental Use Permit application; Non-Food, Indoor Use. Credit 45% of fee toward new active ingredient application that follows. A528............................. 99 Experimental Use Permit 15 22,337 application, Food Use; Requires Tolerance or Tolerance Exemption. A529............................. 100 Amendment to Experimental Use 9 11,429 Permit; requires data review or risk assessment. A571............................. 102 Science reassessment: Cancer 18 95,724 risk, refined ecological risk, and/or endangered species; applicant-initiated. ---------------------------------------------------------------------------------------------------------------- C. Biopesticides and Pollution Prevention Division (BPPD) The Biopesticides and Pollution Prevention Division of OPP is responsible for the processing of pesticide applications for biochemical pesticides, microbial pesticides, and plant-incorporated protectants (PIPs). The fee tables for BPPD actions are presented by type of pesticide rather than by type of action: Microbial and biochemical pesticides, straight chain lepidopteran pheromones (SCLPs), and PIPs. Within each table, the types of application are the same as those in other divisions. Tables 11 through 17 cover BPPD actions. Table 11--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; New Active Ingredients ---------------------------------------------------------------------------------------------------------------- FY'16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- B580............................. 103 New active ingredient; food 19 51,053 use; petition to establish a tolerance. B590............................. 104 New active ingredient; food 17 31,910 use; petition to establish a tolerance exemption. B600............................. 105 New active ingredient; non- 13 19,146 food use. B610............................. 106 New active ingredient; 10 12,764 Experimental Use Permit application; petition to establish a temporary tolerance or temporary tolerance exemption. B611............................. 107 New active ingredient; 12 12,764 Experimental Use Permit application; petition to establish permanent tolerance exemption. B612............................. 108 New active ingredient; no 10 17,550 change to a permanent tolerance exemption. B613............................. 109 New active ingredient; 11 17,550 petition to convert a temporary tolerance or a temporary tolerance exemption to a permanent tolerance or tolerance exemption. B620............................. 110 New active ingredient; 7 6,383 Experimental Use Permit application; non-food use including crop destruct. ---------------------------------------------------------------------------------------------------------------- [[Page 57173]] Table 12--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; New Uses ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- B630............................. 111 First food use; petition to 13 12,764 establish a tolerance exemption. B631............................. 112 New food use; petition to 12 12,764 amend an established tolerance. B640............................. 113 New food use; petition to 19 19,146 amend an established tolerance. B642............................. 115 First food use; indoor; food/ 12 31,910 food handling. B643............................. 114 New Food use; petition to 10 12,764 amend tolerance exemption. B644............................. 116 New use, no change to an 8 12,764 established tolerance or tolerance exemption. B650............................. 117 New use; non-food............ 7 6,383 ---------------------------------------------------------------------------------------------------------------- Table 13--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; New Products ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- B652............................. 118 New product; registered 13 12,764 source of active ingredient; requires petition to amend established tolerance or tolerance exemption; requires (1) submission of product specific data; or (2) citation of previously reviewed and accepted data; or (3) submission or citation of data generated at government expense; or (4) submission or citation of scientifically-sound rationale based on publicly available literature or other relevant information that addresses the data requirement; or (5) submission of a request for a data requirement to be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. B660............................. 119 New product; registered 4 1,278 source of active ingredient(s); identical or substantially similar in composition and use to a registered product; no change in an established tolerance or tolerance exemption No data review, or only product chemistry data; cite-all data citation, or selective data citation where applicant owns all required data or authorization from data owner is demonstrated Category includes 100% re- package of registered end- use or manufacturing-use product that requires no data submission or data matrix For microbial pesticides, the active ingredient(s) must not be re- isolated. B670............................. 120 New product; registered 7 5,107 source of active ingredient(s); no change in an established tolerance or tolerance exemption; requires: (1) Submission of product specific data; or (2) citation of previously reviewed and accepted data; or (3) submission or citation of data generated at government expense; or (4) submission or citation of a scientifically-sound rationale based on publicly available literature or other relevant information that addresses the data requirement; or (5) submission of a request for a data requirement to be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. B671............................. 121 New product; unregistered 17 12,764 source of active ingredient(s); requires a petition to amend an established tolerance or tolerance exemption; requires: (1) Submission of product specific data; or (2) citation of previously reviewed and accepted data; or (3) submission or citation of data generated at government expense; or (4) submission or citation of a scientifically-sound rationale based on publicly available literature or other relevant information that addresses the data requirement; or (5) submission of a request for a data requirement to be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. B672............................. 122 New product; unregistered 13 9,118 source of active ingredient(s); non-food use or food use with a tolerance or tolerance exemption previously established for the active ingredient(s); requires: (1) Submission of product specific data; or (2) citation of previously reviewed and accepted data; or (3) submission or citation of data generated at government expense; or (4) submission or citation of a scientifically-sound rationale based on publicly available literature or other relevant information that addresses the data requirement; or (5) submission of a request for a data requirement to be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. B673............................. 123 New product MUP/EP; 10 5,107 unregistered source of active ingredient(s); citation of Technical Grade Active Ingredient (TGAI) data previously reviewed and accepted by the Agency Requires an Agency determination that the cited data supports the new product. B674............................. 124 New product MUP; Repack of 4 1,278 identical registered end-use product as a manufacturing- use product; same registered uses only. [[Page 57174]] B675............................. 125 New Product MUP; registered 10 9,118 source of active ingredient; submission of completely new generic data package; registered uses only. B676............................. 126 New product; more than one 13 9,118 active ingredient where one active ingredient is an unregistered source; product chemistry data must be submitted; requires: (1) Submission of product specific data, and (2) citation of previously reviewed and accepted data; or (3) submission or citation of data generated at government expense; or (4) submission or citation of a scientifically-sound rationale based on publicly available literature or other relevant information that addresses the data requirement; or (5) submission of a request for a data requirement to be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. B677............................. 127 New end-use non-food animal 10 8,820 product with submission of two or more target animal safety studies; includes data and/or waivers of data. ---------------------------------------------------------------------------------------------------------------- Table 14--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; Amendments ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- B621............................. 128 Amendment; Experimental Use 7 5,107 Permit; no change to an established temporary tolerance or tolerance exemption. B622............................. 129 Amendment; Experimental Use 11 12,764 Permit; petition to amend an established or temporary tolerance or tolerance exemption. B641............................. 130 Amendment of an established 13 12,764 tolerance or tolerance exemption. B680............................. 131 Amendment; registered source 5 5,107 of active ingredient(s); no new use(s); no changes to an established tolerance or tolerance exemption Requires data submission. B681............................. 132 Amendment; unregistered 7 6,079 source of active ingredient(s) Requires data submission. B683............................. 133 Label amendment; requires 6 5,107 review/update of previous risk assessment(s) without data submission (eg., labeling changes to REI, PPE, PHI). B684............................. 134 Amending non-food animal 8 8,820 product that includes submission of target animal safety data; previously registered. ---------------------------------------------------------------------------------------------------------------- Table 15--Biopesticides and Pollution Prevention Division--Straight Chain Lepidopteran Pheromones (SCLPS) ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- B690............................. 135 New active ingredient; food 7 2,554 or non-food use. B700............................. 136 Experimental Use Permit 7 1,278 application; new active ingredient or new use. B701............................. 137 Extend or amend Experimental 4 1,278 Use Permit. B710............................. 138 New product; registered 4 1,278 source of active ingredient(s); identical or substantially similar in composition and use to a registered product; no change in an established tolerance or tolerance exemption No data review, or only product chemistry data; cite-all data citation, or selective data citation where applicant owns all required data or authorization from data owner is demonstrated Category includes 100% re- package of registered end- use or manufacturing-use product that requires no data submission or data matrix. B720............................. 139 New product; registered 5 1,278 source of active ingredient(s); requires: (1) Submission of product specific data; or (2) citation of previously reviewed and accepted data; or (3) submission or citation of data generated at government expense; or (4) submission or citation of a scientifically-sound rationale based on publicly available literature or other relevant information that addresses the data requirement; or (5) submission of a request for a data requirement to be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. B721............................. 140 New product; unregistered 7 2,676 source of active ingredient. [[Page 57175]] B722............................. 141 New use and/or amendment; 7 2,477 petition to establish a tolerance or tolerance exemption. B730............................. 142 Label amendment requiring 5 1,278 data submission. ---------------------------------------------------------------------------------------------------------------- Table 16--Biopesticides and Pollution Prevention Division--Other Actions ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- B614............................. 143 Conditional Ruling on 3 2,530 Preapplication Study Waivers; applicant-initiated. B615............................. 144 Rebuttal of agency reviewed 3 2,530 protocol, applicant initiated. B682............................. 145 Protocol review; applicant 3 2,432 initiated; excludes time for HSRB review. ---------------------------------------------------------------------------------------------------------------- Table 17--Biopesticides and Pollution Prevention Division--Plant Incorporated Protectants (PIPS) ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- B740............................. 146 Experimental Use Permit 6 95,724 application; no petition for tolerance/tolerance exemption. Includes: Non- food/feed use(s) for a new or registered PIP; food/feed use(s) for a new or registered PIP with crop destruct; food/feed use(s) for a new or registered PIP in which an established tolerance/tolerance exemption exists for the intended use(s). B750............................. 147 Experimental Use Permit 9 127,630 application; with a petition to establish a temporary or permanent tolerance/ tolerance exemption for the active ingredient. Includes new food/feed use for a registered PIP. B770............................. 148 Experimental Use Permit 15 191,444 application; new PIP; with petition to establish a temporary tolerance/ tolerance exemption for the active ingredient; credit 75% of B771 fee toward registration application for a new active ingredient that follows; SAP review. B771............................. 149 Experimental Use Permit 10 127,630 application; new PIP; with petition to establish a temporary tolerance/ tolerance exemption for the active ingredient; credit 75% of B771 fee toward registration application for a new active ingredient that follows. B772............................. 150 Application to amend or 3 12,764 extend an Experimental Use Permit; no petition since the established tolerance/ tolerance exemption for the active ingredient is unaffected. B773............................. 151 Application to amend or 5 31,910 extend an Experimental Use Permit; with petition to extend a temporary tolerance/ tolerance exemption for the active ingredient. B780............................. 152 Registration application; new 12 159,537 PIP; non-food/feed. B790............................. 153 Registration application; new 18 223,351 PIP; non-food/feed; SAP review. B800............................. 154 Registration application; new 12 255,324 PIP; with petition to establish permanent tolerance/tolerance exemption for the active ingredient based on an existing temporary tolerance/ tolerance exemption. B810............................. 155 Registration application; new 18 319,072 PIP; with petition to establish permanent tolerance/tolerance exemption for the active ingredient based on an existing temporary tolerance/ tolerance exemption. SAP review. B820............................. 156 Registration application; new 15 319,072 PIP; with petition to establish or amend a permanent tolerance/ tolerance exemption of an active ingredient. B840............................. 157 Registration application; new 21 382,886 PIP; with petition to establish or amend a permanent tolerance/ tolerance exemption of an active ingredient. SAP review. B851............................. 158 Registration application; new 9 127,630 event of a previously registered PIP active ingredient(s); no petition since permanent tolerance/ tolerance exemption is already established for the active ingredient(s). B870............................. 159 Registration application; 9 38,290 registered PIP; new product; new use; no petition since a permanent tolerance/ tolerance exemption is already established for the active ingredient(s). [[Page 57176]] B880............................. 160 Registration application; 9 31,910 registered PIP; new product or new terms of registration; additional data submitted; no petition since a permanent tolerance/ tolerance exemption is already established for the active ingredient(s). B881............................. 161 Registration application; 15 95,724 registered PIP; new product or new terms of registration; additional data submitted; no petition since a permanent tolerance/ tolerance exemption is already established for the active ingredient(s). SAP review. B883............................. 162 Registration application; new 9 127,630 PIP, seed increase with negotiated acreage cap and time-limited registration; with petition to establish a permanent tolerance/ tolerance exemption for the active ingredient based on an existing temporary tolerance/tolerance exemption. B884............................. 163 Registration application; new 12 159,537 PIP, seed increase with negotiated acreage cap and time-limited registration; with petition to establish a permanent tolerance/ tolerance exemption for the active ingredient. B885............................. 164 Registration application; 9 95,724 registered PIP, seed increase; breeding stack of previously approved PIPs, same crop; no petition since a permanent tolerance/ tolerance exemption is already established for the active ingredient(s). B890............................. 165 Application to amend a seed 9 63,816 increase registration; converts registration to commercial registration; no petition since permanent tolerance/tolerance exemption is already established for the active ingredient(s). B891............................. 166 Application to amend a seed 15 127,630 increase registration; converts registration to a commercial registration; no petition since a permanent tolerance/tolerance exemption already established for the active ingredient(s); SAP review. B900............................. 167 Application to amend a 6 12,764 registration, including actions such as extending an expiration date, modifying an IRM plan, or adding an insect to be controlled. B901............................. 168 Application to amend a 12 76,578 registration, including actions such as extending an expiration date, modifying an IRM plan, or adding an insect to be controlled. SAP review. B902............................. 169 PIP Protocol review.......... 3 6,383 B903............................. 170 Inert ingredient tolerance 6 63,816 exemption; e.g., a marker such as NPT II; reviewed in BPPD. B904............................. 171 Import tolerance or tolerance 9 127,630 exemption; processed commodities/food only (inert or active ingredient). ---------------------------------------------------------------------------------------------------------------- Table 18--Inert Ingredients ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- I001............................. 172 Approval of new food use 12 19,845 inert ingredient. I002............................. 173 Amend currently approved 10 5,513 inert ingredient tolerance or exemption from tolerance; new data. I003............................. 174 Amend currently approved 8 3,308 inert ingredient tolerance or exemption from tolerance; no new data. I004............................. 175 Approval of new non-food use 8 11,025 inert ingredient. I005............................. 176 Amend currently approved non- 8 5,513 food use inert ingredient with new use pattern; new data. I006............................. 177 Amend currently approved non- 6 3,308 food use inert ingredient with new use pattern; no new data. I007............................. 178 Approval of substantially 4 1,654 similar non-food use inert ingredients when original inert is compositionally similar with similar use pattern. I008............................. 179 Approval of new polymer inert 5 3,749 ingredient, food use. I009............................. 180 Approval of new polymer inert 4 3,087 ingredient, non food use. I010............................. 181 Petition to amend a tolerance 6 1,654 exemption descriptor to add one or more CASRNs; no new data. ---------------------------------------------------------------------------------------------------------------- [[Page 57177]] Table 19--Miscellaneous Actions ---------------------------------------------------------------------------------------------------------------- FY '16/17 Decision registration EPA No. New CR No. Action review time service fee (months) ($) ---------------------------------------------------------------------------------------------------------------- M001............................. 182 Study protocol requiring 9 7,938 Human Studies Review Board review as defined in 40 CFR Part 26 in support of an active ingredient. M002............................. 183 Completed study requiring 9 7,938 Human Studies Review Board review as defined in 40 CFR Part 26 in support of an active ingredient. M003............................. 184 External technical peer 12 63,945 review of new active ingredient, product, or amendment (e.g., consultation with FIFRA Scientific Advisory Panel) for an action with a decision timeframe of less than 12 months. Applicant initiated request based on a requirement of the Administrator, as defined by FIFRA Sec. 25(d), in support of a novel active ingredient, or unique use pattern or application technology. Excludes PIP active ingredients. M004............................. 185 External technical peer 18 63,945 review of new active ingredient, product, or amendment (e.g., consultation with FIFRA Scientific Advisory Panel) for an action with a decision timeframe of greater than 12 months. Applicant initiated request based on a requirement of the Administrator, as defined by FIFRA Sec. 25(d), in support of a novel active ingredient, or unique use pattern or application technology. Excludes PIP active ingredients. M005............................. 186 New Product: Combination, 9 22,050 Contains a combination of active ingredients from a registered and/or unregistered source; conventional, antimicrobial and/or biopesticide. Requires coordination with other regulatory divisions to conduct review of data, label and/or verify the validity of existing data as cited. Only existing uses for each active ingredient in the combination product. M006............................. 187 Request for up to 5 letters 1 277 of certification (Gold Seal) for one actively registered product. M007............................. 188 Request to extend Exclusive 12 5,513 Use of data as provided by FIFRA Section 3(c)(1)(F)(ii). M008............................. 189 Request to grant Exclusive 10 1,654 Use of data as provided by FIFRA Section 3(c)(1)(F)(vi) for a minor use, when a FIFRA Section 2(ll)(2) determination is required. ---------------------------------------------------------------------------------------------------------------- V. How To Pay Fees Applicants must submit fee payments at the time of application, and EPA will reject any application that does not contain evidence that the fee has been paid. EPA has developed a Web site at http://www.epa.gov/pesticides/fees/tool/index.htm to help applicants identify the fee category and the fee. All fees should be rounded up to the whole dollar. Due to changes mandated by the U.S. Department of the Treasury, checks, bank drafts and money orders are no longer acceptable as of September 30, 2015. Credit card payments are only acceptable for amounts less than or equal to $25,000. All payments above $25,000 can be made by electronic funds transfer via www.pay.gov. A. Online You may pay electronically through the government payment Web site www.pay.gov. 1. From the pay.gov home page, under ``Find Public Forms.'' 2. Select ``search by Agency name.'' 3. On the A-Z Index of Forms page, select ``E.'' 4. Select ``Environmental Protection Agency.'' 5. From the list of forms, select ``Pre-payment of Pesticide Registration Improvement Act Fee.'' 6. Complete the form entering the PRIA fee category and fee. 7. Keep a copy of the pay.gov acknowledgement of payment. A copy of the acknowledgement must be printed and attached to the front of the application to assure that EPA can match the application with the payment. VI. How To Submit Applications Submissions to the Agency should be made at the address given in Unit VII. The applicant should attach documentation that the fee has been paid which in most cases will be pay.gov payment acknowledgement. If the applicant is applying for a fee waiver, the applicant should provide sufficient documentation as described in FIFRA section 33(b)(7) and http://www.epa.gov/pesticides/fees/questions/waivers.htm. The fee waiver request should be easy to identify and separate from the rest of the application and submitted with documentation that at least 25% of the fee has been paid. If evidence of fee payment (electronic acknowledgement) is not submitted with the application, EPA will reject the application and will not process it further. After EPA receives an application and payment, EPA performs a screen on the application to determine that the category is correct and that the proper fee amount has been paid. If either is incorrect, EPA will notify the applicant and require payment of any additional amount due. A refund will be provided in case of an overpayment. EPA will not process the application further until the proper fee has been paid for the category of application or a request for a fee waiver accompanies the application and the appropriate portion of the fee has been paid. EPA will assign a unique identification number to each covered application for which payment has been made. EPA notifies the applicant of the unique identification number. This information is sent by email if EPA has either an email address on file or an email address is provided on the application. VII. Addresses for Applications New covered applications should be identified in the title line with the mail code REGFEE. By U.S. Postal Service mail. Document Processing Desk (REGFEE), Office of Pesticide Programs (7504P), U.S. Environmental Protection Agency, 1200 Pennsylvania Avenue NW., Washington, DC 20460- 0001. [[Page 57178]] By courier. Document Processing Desk (REGFEE), Office of Pesticide Programs, U.S. Environmental Protection Agency, Room S-4400, One Potomac Yard (South Bldg.), 2777 S. Crystal Drive, Arlington, VA 22202-4501. Couriers and delivery personnel must present a valid picture identification card to gain access to the building. Hours of operation for the Document Processing Desk are 8 a.m. to 4:30 p.m., Monday through Friday, excluding Federal holidays. List of Subjects Environmental protection, Administrative practice and procedure, Pesticides. Dated: September 15, 2015. Marty Monell, Acting Director, Office of Pesticide Programs. [FR Doc. 2015-24064 Filed 9-21-15; 8:45 am] BILLING CODE 6560-50-P
![57166 Federal Register / Vol. 80, No. 183 / Tuesday, September 22, 2015 / Notices
DEPARTMENT OF ENERGY Filed Date: 9/10/15. FOR FURTHER INFORMATION CONTACT:
Accession Number: 20150910–5137. Peter Caulkins (7501P), Immediate
Federal Energy Regulatory Comments Due: 5 p.m. ET 10/1/15. Office, Office of Pesticide Programs,
Commission Docket Numbers: ER15–2640–000. Environmental Protection Agency, 1200
Applicants: New York Independent Pennsylvania Ave. NW., Washington,
Combined Notice of Filings #2 DC 20460–0001; telephone number:
System Operator, In.
Take notice that the Commission Description: § 205(d) Rate Filing: (703) 305–6550; fax number: (703) 308–
received the following electric rate NYISO 205 filing of tariff revision to 4776; email address: caulkins.peter@
filings: implement external CTS with ISO–NE epa.gov.
Docket Numbers: ER13–521–002; to be effective 12/31/9998. SUPPLEMENTARY INFORMATION:
ER13–520–002; ER13–1442–002; ER13– Filed Date: 9/10/15.
1441–002; ER13–1273–002; ER13–1272– Accession Number: 20150910–5138. I. General Information
002; ER13–1271–002; ER13–1270–002; Comments Due: 5 p.m. ET 10/1/15. A. Does this action apply to me?
ER13–1269–002; ER13–1268–002; The filings are accessible in the You may be potentially affected by
ER13–1267–002; ER13–1266–003; Commission’s eLibrary system by this action if you register pesticide
ER12–21–013; ER12–1626–003; ER10– clicking on the links or querying the products under the Federal Insecticide,
3246–003; ER10–2605–006; ER10–2475– docket number.
Fungicide, and Rodenticide Act
006; ER10–2474–006; EL15–22–000. Any person desiring to intervene or
Applicants: Nevada Power Company, (FIFRA). Potentially affected entities
protest in any of the above proceedings may include, but are not limited to:
Sierra Pacific Power Company, must file in accordance with Rules 211 • Agricultural pesticide
PacifiCorp, Agua Caliente Solar, LLC, and 214 of the Commission’s manufacturers (NAICS code 32532).
Pinyon Pines Wind I, LLC, Pinyon Pines Regulations (18 CFR 385.211 and
• Antimicrobial pesticide
Wind II, LLC, Solar Star California XIX, 385.214) on or before 5:00 p.m. Eastern manufacturers (NAICS code 32561).
LLC, Solar Star California XX, LLC, time on the specified comment date. • Antifoulant pesticide manufacturers
Topaz Solar Farms LLC, CalEnergy, Protests may be considered, but (NAICS code 32551).
LLC, CE Leathers Company, Del Ranch intervention is necessary to become a • Wood preservative manufacturers
Company, Elmore Company, Fish Lake party to the proceeding. (NAICS code 32519).
Power LLC, Salton Sea Power eFiling is encouraged. More detailed This listing is not intended to be
Generation Company, Salton Sea Power information relating to filing exhaustive, but rather provides a guide
L.L.C., Vulcan/BN Geothermal Power requirements, interventions, protests, for readers regarding entities likely to be
Company, Yuma Cogeneration service, and qualifying facilities filings affected by this action. Other types of
Associates, MidAmerican Energy can be found at: http://www.ferc.gov/ entities not listed in this unit could also
Company, Bishop Hill Energy II LLC, docs-filing/efiling/filing-req.pdf. For be affected. The North American
Cordova Energy Company LLC, Power other information, call (866) 208–3676 Industrial Classification System
Resources, Ltd., Saranac Power Partners, (toll free). For TTY, call (202) 502–8659. (NAICS) codes have been provided to
L.P. assist you and others in determining
Description: Supplemental Filing of Dated: September 10, 2015.
Nathaniel J. Davis, Sr.,
whether this action might apply to
WorkPapers of the BHE MBR Sellers. certain entities. To determine whether
Filed Date: 9/8/15. Deputy Secretary.
you or your business may be affected by
Accession Number: 20150909–0026. [FR Doc. 2015–23982 Filed 9–21–15; 8:45 am]
Comments Due: 5 p.m. ET 9/29/15. this action, you should carefully
BILLING CODE 6717–01–P examine the applicability provisions in
Docket Numbers: ER15–2338–001.
Applicants: Midcontinent the notice and in FIFRA section 33. If
Independent System Operator, Inc., you have any questions regarding the
ENVIRONMENTAL PROTECTION applicability of this action to a
Ameren Transmission Company of
AGENCY particular entity, consult the person
Illinois.
Description: Tariff Amendment: listed under FOR FURTHER INFORMATION
[EPA–HQ–OPP–2015–0614; FRL–9933–75]
2015–09–10_ATXI Supplemental CONTACT.
Depreciation Rate Filing to be effective Pesticides; Revised Fee Schedule for B. How can I get copies of this document
10/1/2015. Registration Applications and other related information?
Filed Date: 9/10/15.
Accession Number: 20150910–5110. AGENCY: Environmental Protection The docket for this action, identified
Comments Due: 5 p.m. ET 9/17/15. Agency (EPA). by docket identification (ID) number
Docket Numbers: ER15–2638–000. ACTION : Notice. EPA–HQ–OPP–2015–0614, is available
Applicants: Louisville Gas and at http://www.regulations.gov or at the
Electric Company. SUMMARY: EPA is publishing a revised Office of Pesticide Programs Regulatory
Description: § 205(d) Rate Filing: list of pesticide registration service fees Public Docket (OPP Docket) in the
Modifications to Attachment C to be applicable to specified pesticide Environmental Protection Agency
effective 11/10/2015. applications and tolerance actions. Docket Center (EPA/DC), EPA West
Filed Date: 9/10/15. Under the Pesticide Registration Bldg., Rm. 3334, 1301 Constitution Ave.
Accession Number: 20150910–5112. Improvement Extension Act, the NW., Washington, DC 20460–0001. The
Comments Due: 5 p.m. ET 10/1/15 registration service fees for covered Public Reading Room is open from 8:30
tkelley on DSK3SPTVN1PROD with NOTICES
Docket Numbers: ER15–2639–000. pesticide registration applications a.m. to 4:30 p.m., Monday through
Applicants: CenterPoint Energy received on or after October 1, 2015, Friday, excluding legal holidays. The
Houston Electric, LLC. increase by 5% rounding up to the telephone number for the Public
Description: § 205(d) Rate Filing: TFO nearest dollar from the fees published Reading Room is (202) 566–1744, and
Tariff Interim Rate Revision to Conform for fiscal year 2015. The new fees for the telephone number for the OPP
with PUCT-Approved ERCOT Rate to be FY’2016 become effective on October 1, Docket is (703) 305–5805. Please review
effective 8/17/2015. 2015. the visitor instructions and additional
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![57178 Federal Register / Vol. 80, No. 183 / Tuesday, September 22, 2015 / Notices
• By courier. Document Processing DATES: Written comments on the consent decree from persons who were
Desk (REGFEE), Office of Pesticide proposed consent decree must be not named as parties or intervenors to
Programs, U.S. Environmental received by October 22, 2015. the litigation in question. EPA or the
Protection Agency, Room S–4400, One ADDRESSES: Submit your comments, Department of Justice may withdraw or
Potomac Yard (South Bldg.), 2777 S. identified by Docket ID number EPA– withhold consent to the proposed
Crystal Drive, Arlington, VA 22202– HQ–OGC–2015–0636, online at consent decree if the comments disclose
4501. www.regulations.gov (EPA’s preferred facts or considerations that indicate that
Couriers and delivery personnel must method); by email to oei.docket@ such consent is inappropriate,
present a valid picture identification epa.gov; by mail to EPA Docket Center, improper, inadequate, or inconsistent
card to gain access to the building. Environmental Protection Agency, with the requirements of the Act. Unless
Hours of operation for the Document Mailcode: 2822T, 1200 Pennsylvania EPA or the Department of Justice
Processing Desk are 8 a.m. to 4:30 p.m., Ave. NW., Washington, DC 20460–0001; determines that consent to this consent
Monday through Friday, excluding or by hand delivery or courier to EPA decree should be withdrawn, the terms
Federal holidays. Docket Center, EPA West, Room 3334, of the decree will be affirmed.
List of Subjects 1301 Constitution Ave. NW., II. Additional Information About
Washington, DC, between 8:30 a.m. and Commenting on the Proposed Consent
Environmental protection, 4:30 p.m. Monday through Friday, Decree
Administrative practice and procedure, excluding legal holidays. Comments on
Pesticides. a disk or CD–ROM should be formatted A. How can I get a copy of the consent
Dated: September 15, 2015. in Word or ASCII file, avoiding the use decree?
Marty Monell, of special characters and any form of The official public docket for this
Acting Director, Office of Pesticide Programs. encryption, and may be mailed to the action (identified by Docket ID No.
mailing address above. EPA–HQ–OGC–2015–0636) contains a
[FR Doc. 2015–24064 Filed 9–21–15; 8:45 am]
FOR FURTHER INFORMATION CONTACT: M. copy of the proposed consent decree.
BILLING CODE 6560–50–P
Lea Anderson, Air and Radiation Law The official public docket is available
Office (2344A), Office of General for public viewing at the Office of
ENVIRONMENTAL PROTECTION Counsel, U.S. Environmental Protection Environmental Information (OEI) Docket
AGENCY Agency, 1200 Pennsylvania Ave. NW., in the EPA Docket Center, EPA West,
Washington, DC 20460; telephone: (202) Room 3334, 1301 Constitution Ave.
564–5571; fax number (202) 564–5603; NW., Washington, DC. The EPA Docket
[EPA–HQ–OGC–2015–0636; FRL–9934–48–
OGC] email address: anderson.lea@epa.gov. Center Public Reading Room is open
SUPPLEMENTARY INFORMATION: from 8:30 a.m. to 4:30 p.m., Monday
Proposed Consent Decree, Clean Air through Friday, excluding legal
I. Additional Information About the holidays. The telephone number for the
Act Citizen Suit
Proposed Consent Decree Public Reading Room is (202) 566–1744,
AGENCY: Environmental Protection On October 30, 2012, EPA partially and the telephone number for the OEI
Agency (EPA). disapproved a revision to the Utah SIP Docket is (202) 566–1752.
ACTION: Notice of proposed consent intended to address the regional haze An electronic version of the public
decree; request for public comment. requirements of the Clean Air Act. 77 docket is available through
FR 74355 (Dec. 14, 2012). When EPA www.regulations.gov. You may use
SUMMARY: In accordance with section disapproves a SIP submission in whole www.regulations.gov to submit or view
113(g) of the Clean Air Act, as amended or in part, section 110(c) of the Act public comments, access the index
(‘‘CAA’’ or the ‘‘Act’’), notice is hereby requires EPA to promulgate a FIP within listing of the contents of the official
given of a proposed consent decree to two years unless the State corrects the public docket, and to access those
address a lawsuit filed by WildEarth deficiency and EPA approves the plan documents in the public docket that are
Guardians, HEAL Utah, National Parks revision. On July 22, 2015, Plaintiffs available electronically. Once in the
Conservation Association, and Sierra filed an amended consolidated system, key in the appropriate docket
Club (collectively, ‘‘Plaintiffs’’): complaint in the United States District identification number then select
Wildearth Guardians, et al. v. EPA, No. Court for the Northern District of ‘‘search’’.
1:15–cv–00630 (D. CO). In 2012, EPA Colorado alleging that EPA had failed to It is important to note that EPA’s
issued a rule partially disapproving a promulgate a FIP for Utah as required by policy is that public comments, whether
revision to a state implementation plan the Clean Air Act. submitted electronically or in paper,
(SIP) submitted by Utah to address the The proposed consent decree would will be made available for public
State’s ‘‘best available retrofit resolve the lawsuit filed by Plaintiffs by viewing online at www.regulations.gov
technology’’ (‘‘BART’’) determination establishing that EPA must take without change, unless the comment
for Units 1 and 2 of the Hunter power proposed action by November 19, 2015 contains copyrighted material, CBI, or
plant and Units 1 and 2 of the and final action by March 31, 2016, to other information whose disclosure is
Huntingdon power plant. In its lawsuit, address the deficiencies in Utah’s SIP restricted by statute. Information
Plaintiffs alleged that EPA has failed to revision regarding the State’s BART claimed as CBI and other information
meet the requirement of the Clean Air determination for Units 1 and 2 of the whose disclosure is restricted by statute
Act that the Agency promulgate a Hunter power plant and Units 1 and 2 is not included in the official public
tkelley on DSK3SPTVN1PROD with NOTICES
federal implementation plan (FIP) of the Huntingdon power plant. See the docket or in the electronic public
within two years of partially proposed consent decree for the specific docket. EPA’s policy is that copyrighted
disapproving a SIP, in whole or in part. details. material, including copyrighted material
The proposed consent decree For a period of thirty (30) days contained in a public comment, will not
establishes proposed and final deadlines following the date of publication of this be placed in EPA’s electronic public
for EPA to take action to meet its notice, the Agency will accept written docket but will be available only in
obligations with respect to Utah. comments relating to the proposed printed, paper form in the official public
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Document Created: 2015-12-15 09:35:36
Document Modified: 2015-12-15 09:35:36
| 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. | |
| Contact | Peter Caulkins (7501P), Immediate Office, Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; telephone | |
| FR Citation | 80 FR 57166 |
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