Information Collection Request Submitted to OMB for Review and Approval; Comment Request; Allegations of Significant Adverse Reactions to Human Health or the Environment (Renewal), 58905-58906 [2021-23122]

Download as PDF Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices service, and qualifying facilities filings can be found at: https://www.ferc.gov/ docs-filing/efiling/filing-req.pdf. For other information, call (866) 208–3676 (toll free). For TTY, call (202) 502–8659. DEPARTMENT OF ENERGY Federal Energy Regulatory Commission Combined Notice of Filings Take notice that the Commission has received the following Natural Gas Pipeline Rate and Refund Report filings: jspears on DSK121TN23PROD with NOTICES1 Filings Instituting Proceedings 18:00 Oct 22, 2021 Jkt 256001 [FR Doc. 2021–23219 Filed 10–22–21; 8:45 am] BILLING CODE 6717–01–P Docket Numbers: RP21–1178–001. Applicants: Northern Natural Gas Company. Description: Northern Natural Gas Company submits tariff filing per 154.205(b): 20211001 Negotiated Rate Filing to be effective 10/1/2021 under RP21–1178. Filed Date: 10/1/21. Accession Number: 20211001–5099. Comment Date: 5 p.m. ET 10/21/21. Docket Numbers: RP22–55–000. Applicants: Transcontinental Gas Pipe Line Company, LLC. Description: § 4(d) Rate Filing: NonConforming—Leidy South—In-Svc— UGI Utilities to be effective 10/19/2021. Filed Date: 10/18/21. Accession Number: 20211018–5067. Comment Date: 5 p.m. ET 11/1/21. Docket Numbers: RP22–56–000. Applicants: Centra Pipelines Minnesota Inc. Description: § 4(d) Rate Filing: Updated Index Of Shippers Oct 2021 to be effective 12/1/2021. Filed Date: 10/18/21. Accession Number: 20211018–5072. Comment Date: 5 p.m. ET 11/1/21. Docket Numbers: RP22–57–000. Applicants: Transcontinental Gas Pipe Line Company, LLC. Description: § 4(d) Rate Filing: Negotiated Rates—Leidy South—Interim Svc—Coterra Energy to be effective 10/ 19/2021. Filed Date: 10/18/21. Accession Number: 20211018–5123. Comment Date: 5 p.m. ET 11/1/21. Any person desiring to intervene or protest in any of the above proceedings must file in accordance with Rules 211 and 214 of the Commission’s Regulations (18 CFR 385.211 and 385.214) on or before 5:00 p.m. Eastern time on the specified comment date. Protests may be considered, but intervention is necessary to become a party to the proceeding. The filings are accessible in the Commission’s eLibrary system (https:// elibrary.ferc.gov/idmws/search/fercgen search.asp) by querying the docket number. eFiling is encouraged. More detailed information relating to filing requirements, interventions, protests, VerDate Sep<11>2014 Dated: October 19, 2021. Debbie-Anne A. Reese, Deputy Secretary. ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPPT–2015–0688; FRL–9137–01– OMS] Information Collection Request Submitted to OMB for Review and Approval; Comment Request; Allegations of Significant Adverse Reactions to Human Health or the Environment (Renewal) Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: The Environmental Protection Agency (EPA) has submitted an information collection request (ICR), ‘‘Allegations of Significant Adverse Reactions to Human Health or the Environment’’ (EPA ICR Number 1031.12 and OMB Control Number 2070–0017) to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act. This is a proposed extension of the ICR which is currently approved through October 31, 2021. Public comments were previously requested via the Federal Register on March 29, 2021 during a 60-day comment period. This notice allows for an additional 30 days for public comments. A fuller description of the ICR is given below, including its estimated burden and cost to the public. An agency may not conduct or sponsor and a person is not required to respond to a collection of information unless it displays a currently valid OMB control number. DATES: Additional comments may be submitted on or before November 24, 2021. SUMMARY: Submit your comments to EPA, referencing Docket ID No. EPA– HQ–OPPT–2015–0688, online using www.regulations.gov (our preferred method), or by mail to: EPA Docket Center, Environmental Protection Agency, Mail Code 28221T, 1200 Pennsylvania Ave. NW, Washington, DC 20460. EPA’s policy is that all comments received will be included in ADDRESSES: PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 58905 the public docket without change including any personal information provided, unless the comment includes profanity, threats, information claimed to be Confidential Business Information (CBI), or other information whose disclosure is restricted by statute. Submit written comments and recommendations to OMB for the proposed information collection within 30 days of publication of this notice to www.reginfo.gov/public/do/PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. FOR FURTHER INFORMATION CONTACT: Virginia Lee, Data Gathering and Analysis Division (7401M), Office of Pollution Prevention and Toxics, Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460; telephone number: (202) 564– 4142; email address: lee.virginia@ epa.gov. SUPPLEMENTARY INFORMATION: Supporting documents, which explain in detail the information that the EPA will be collecting, are available in the public docket for this ICR. The docket can be viewed online at www.regulations.gov or in person at the EPA Docket Center, WJC West, Room 3334, 1301 Constitution Ave. NW, Washington, DC. The telephone number for the Docket Center is 202–566–1744. For additional information about EPA’s public docket, visit https://www.epa.gov/ dockets. Abstract: Under section 8(c) of the Toxic Substances Control Act (TSCA), 15 U.S.C. 2607(c), companies that manufacture, process, or distribute chemicals are required to maintain records of significant adverse reactions to health or the environment alleged to have been caused by such chemicals. Since TSCA section 8(c) includes no automatic reporting provision, EPA can obtain and use the information contained in company files only by inspecting those files or requiring reporting of records that relate to specific substances of concern. Therefore, under certain conditions, and using the provisions found in 40 CFR part 717, EPA may require companies to report such allegations to the Agency. EPA uses such information on a case specific basis to corroborate suspected adverse health or environmental effects of chemicals already under review by EPA. The information is also useful to identify trends of adverse effects across the industry that may not be apparent to any one chemical company. This ICR addresses the information reporting and E:\FR\FM\25OCN1.SGM 25OCN1 58906 Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices recordkeeping requirements found in 40 CFR part 717. Respondents may claim all or part of a notice confidential. Form Numbers: None. Respondents/Affected Entities: Companies that manufacture, process, import, or distribute in commerce chemical substances or mixtures. Respondent’s obligation to respond: Mandatory (40 CFR part 717). Estimated number of respondents: 13,160 (total). Frequency of response: 1. Total Estimated burden: 25,527 hours (per year). Burden is defined at 5 CFR 1320.03(b). Total Estimated cost: $4,701,622 (per year) includes $0 annualized capital or operation and maintenance costs. Changes in the Estimates: There is no change in the estimated annual burden compared with the ICR currently approved by OMB. There is, however, an increase in the estimated total burden cost from $1,987,487 to $4,701,622 that is related to an adjustment in the burden cost calculation associated with projected compliance determination activities. This change is an adjustment. Courtney Kerwin, Director, Regulatory Support Division. [FR Doc. 2021–23122 Filed 10–22–21; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPP–2021–0513; FRL–9119–01– OCSPP] Notice of Receipt of Requests To Voluntarily Cancel Certain Pesticide Registrations and Amend Registrations To Terminate Certain Uses Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: In accordance with the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), EPA is issuing a notice of receipt of requests by the registrants to voluntarily cancel their registrations of certain products and to amend certain product registrations to SUMMARY: terminate uses. EPA intends to grant these requests at the close of the comment period for this announcement unless the Agency receives substantive comments within the comment period that would merit its further review of the requests, or unless the registrants withdrew their requests. If these requests are granted, any sale, distribution, or use of products listed in this notice will be permitted after the registration has been cancelled and uses terminated only if such sale, distribution, or use is consistent with the terms as described in the final order. DATES: Comments must be received on or before November 24, 2021. ADDRESSES: Submit your comments, identified by docket identification (ID) number EPA–HQ–OPP–2021–0513, through the Federal eRulemaking Portal at https://www.regulations.gov. Follow the online instructions for submitting comments. Do not submit electronically any information you consider to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. Additional instructions on commenting or visiting the docket, along with more information about dockets generally, is available at https://www.epa.gov/dockets. Submit written withdrawal request by mail to: Registration Division (7502P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460–0001. ATTN: Christopher Green. Due to the public health concerns related to COVID–19, the EPA Docket Center (EPA/DC) and Reading Room is closed to visitors with limited exceptions. The staff continues to provide remote customer service via email, phone, and webform. For the latest status information on EPA/DC services and docket access, visit https:// www.epa.gov/dockets. FOR FURTHER INFORMATION CONTACT: Christopher Green, Registration Division (7502P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460–0001; telephone number: (703) 347–0367; email address: green.christopher@epa.gov. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? This action is directed to the public in general and may be of interest to a wide range of stakeholders including environmental, human health, and agricultural advocates; the chemical industry; pesticide users; and members of the public interested in the sale, distribution, or use of pesticides. Since others also may be interested, the Agency has not attempted to describe all the specific entities that may be affected by this action. B. What should I consider as I prepare my comments for EPA? 1. Submitting CBI. Do not submit this information to EPA through regulations.gov or email. Clearly mark the part or all of the information that you claim to be CBI. For CBI information in a disk or CD–ROM that you mail to EPA, mark the outside of the disk or CD–ROM as CBI and then identify electronically within the disk or CD–ROM the specific information that is claimed as CBI. In addition to one complete version of the comment that includes information claimed as CBI, a copy of the comment that does not contain the information claimed as CBI must be submitted for inclusion in the public docket. Information so marked will not be disclosed except in accordance with procedures set forth in 40 CFR part 2. 2. Tips for preparing your comments. When preparing and submitting your comments, see the commenting tips at https://www.epa.gov/dockets/ comments.html. II. What action is the Agency taking? This notice announces receipt by EPA of requests from registrants to cancel and terminate certain uses product registrations. The affected products and the registrants making the requests are identified in Table 1, Table 1A, Table 2 and Table 3 of this unit. Unless a request is withdrawn by the registrant or if the Agency determines that there are substantive comments that warrant further review of this request, EPA intends to issue an order canceling and amending the affected registrations. jspears on DSK121TN23PROD with NOTICES1 TABLE 1—PRODUCT REGISTRATIONS WITH PENDING REQUESTS FOR CANCELLATION Registration No. Company No. 279–3125 279–3248 279–3249 279–3297 279–3298 VerDate Sep<11>2014 279 279 279 279 279 18:00 Oct 22, 2021 Product name Active ingredients Fury 1.5 EC Insecticide .............................................. Z-Cype 0.8 EW Insecticide ........................................ Z-Cype 0.8 EC Insecticide ......................................... 0.344% F0570 OTC Granular Insecticide .................. 0.258% F0570 OTC Granular Insecticide .................. Jkt 256001 PO 00000 Frm 00048 Fmt 4703 Sfmt 4703 Zeta-Cypermethrin. Zeta-Cypermethrin. Zeta-Cypermethrin. Zeta-Cypermethrin. Zeta-Cypermethrin. E:\FR\FM\25OCN1.SGM 25OCN1

Agencies

[Federal Register Volume 86, Number 203 (Monday, October 25, 2021)]
[Notices]
[Pages 58905-58906]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-23122]


=======================================================================
-----------------------------------------------------------------------

ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPPT-2015-0688; FRL-9137-01-OMS]


Information Collection Request Submitted to OMB for Review and 
Approval; Comment Request; Allegations of Significant Adverse Reactions 
to Human Health or the Environment (Renewal)

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Environmental Protection Agency (EPA) has submitted an 
information collection request (ICR), ``Allegations of Significant 
Adverse Reactions to Human Health or the Environment'' (EPA ICR Number 
1031.12 and OMB Control Number 2070-0017) to the Office of Management 
and Budget (OMB) for review and approval in accordance with the 
Paperwork Reduction Act. This is a proposed extension of the ICR which 
is currently approved through October 31, 2021. Public comments were 
previously requested via the Federal Register on March 29, 2021 during 
a 60-day comment period. This notice allows for an additional 30 days 
for public comments. A fuller description of the ICR is given below, 
including its estimated burden and cost to the public. An agency may 
not conduct or sponsor and a person is not required to respond to a 
collection of information unless it displays a currently valid OMB 
control number.

DATES: Additional comments may be submitted on or before November 24, 
2021.

ADDRESSES: Submit your comments to EPA, referencing Docket ID No. EPA-
HQ-OPPT-2015-0688, online using www.regulations.gov (our preferred 
method), or by mail to: EPA Docket Center, Environmental Protection 
Agency, Mail Code 28221T, 1200 Pennsylvania Ave. NW, Washington, DC 
20460. EPA's policy is that all comments received will be included in 
the public docket without change including any personal information 
provided, unless the comment includes profanity, threats, information 
claimed to be Confidential Business Information (CBI), or other 
information whose disclosure is restricted by statute.
    Submit written comments and recommendations to OMB for the proposed 
information collection within 30 days of publication of this notice to 
www.reginfo.gov/public/do/PRAMain. Find this particular information 
collection by selecting ``Currently under 30-day Review--Open for 
Public Comments'' or by using the search function.

FOR FURTHER INFORMATION CONTACT: Virginia Lee, Data Gathering and 
Analysis Division (7401M), Office of Pollution Prevention and Toxics, 
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, 
DC 20460; telephone number: (202) 564-4142; email address: 
[email protected].

SUPPLEMENTARY INFORMATION: Supporting documents, which explain in 
detail the information that the EPA will be collecting, are available 
in the public docket for this ICR. The docket can be viewed online at 
www.regulations.gov or in person at the EPA Docket Center, WJC West, 
Room 3334, 1301 Constitution Ave. NW, Washington, DC. The telephone 
number for the Docket Center is 202-566-1744. For additional 
information about EPA's public docket, visit https://www.epa.gov/dockets.
    Abstract: Under section 8(c) of the Toxic Substances Control Act 
(TSCA), 15 U.S.C. 2607(c), companies that manufacture, process, or 
distribute chemicals are required to maintain records of significant 
adverse reactions to health or the environment alleged to have been 
caused by such chemicals. Since TSCA section 8(c) includes no automatic 
reporting provision, EPA can obtain and use the information contained 
in company files only by inspecting those files or requiring reporting 
of records that relate to specific substances of concern. Therefore, 
under certain conditions, and using the provisions found in 40 CFR part 
717, EPA may require companies to report such allegations to the 
Agency. EPA uses such information on a case specific basis to 
corroborate suspected adverse health or environmental effects of 
chemicals already under review by EPA. The information is also useful 
to identify trends of adverse effects across the industry that may not 
be apparent to any one chemical company. This ICR addresses the 
information reporting and

[[Page 58906]]

recordkeeping requirements found in 40 CFR part 717. Respondents may 
claim all or part of a notice confidential.
    Form Numbers: None.
    Respondents/Affected Entities: Companies that manufacture, process, 
import, or distribute in commerce chemical substances or mixtures.
    Respondent's obligation to respond: Mandatory (40 CFR part 717).
    Estimated number of respondents: 13,160 (total).
    Frequency of response: 1.
    Total Estimated burden: 25,527 hours (per year). Burden is defined 
at 5 CFR 1320.03(b).
    Total Estimated cost: $4,701,622 (per year) includes $0 annualized 
capital or operation and maintenance costs.
    Changes in the Estimates: There is no change in the estimated 
annual burden compared with the ICR currently approved by OMB. There 
is, however, an increase in the estimated total burden cost from 
$1,987,487 to $4,701,622 that is related to an adjustment in the burden 
cost calculation associated with projected compliance determination 
activities. This change is an adjustment.

Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2021-23122 Filed 10-22-21; 8:45 am]
BILLING CODE 6560-50-P
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