Information Collection Request Submitted to OMB for Review and Approval; Comment Request; Plant-Incorporated Protectants; CBI Substantiation and Adverse Effects Reporting, 25452-25453 [2018-11802]
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[FR Doc. 2018–11773 Filed 5–31–18; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2017–0440; FRL–9978–73–
OEI]
Information Collection Request
Submitted to OMB for Review and
Approval; Comment Request; PlantIncorporated Protectants; CBI
Substantiation and Adverse Effects
Reporting
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The Environmental Protection
Agency (EPA) has submitted the
following information collection request
(ICR) to the Office of Management and
Budget (OMB) for review and approval
in accordance with the Paperwork
Reduction Act (PRA): ‘‘PlantIncorporated Protectants; CBI
Substantiation and Adverse Effects
Reporting’’ (EPA ICR No. 1693.09, OMB
daltland on DSKBBV9HB2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:06 May 31, 2018
Jkt 244001
Control No. 2070–0142). This is a
request to renew the approval of an
existing ICR, which is currently
approved through May 31, 2018. EPA
did not receive any public comments in
response to the previously provided
public review opportunity issued in the
Federal Register of September 13, 2017.
With this submission to OMB, EPA is
providing an additional 30 days for
public review and comment. 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 July 2, 2018.
ADDRESSES: Submit your comments,
identified by Docket ID number EPA–
HQ–OPP–2017–0440, to both EPA and
OMB as follows:
• To EPA online using https://
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, and
• To OMB via email to oira_
submission@omb.eop.gov. Address
comments to the OMB Desk Officer for
EPA.
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.
FOR FURTHER INFORMATION CONTACT:
Ryne Yarger, Field and External Affairs
Division, 7506P, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460;
telephone number: 703–605–1193; fax
number: 703–305–5884; email address:
yarger.ryne@epa.gov.
SUPPLEMENTARY INFORMATION:
Docket: Supporting documents,
including the ICR that explains in detail
the information collection activities and
the related burden and cost estimates
that are summarized in this document,
are available in the docket for this ICR.
The docket can be viewed online at
https://www.regulations.gov or in person
at the EPA Docket Center, West William
Jefferson Clinton Bldg., Rm. 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: This ICR addresses the two
information collection requirements
PO 00000
Frm 00028
Fmt 4703
Sfmt 4703
contained in the regulations codified in
40 CFR part 174 pertaining to pesticidal
substances that are produced by plants
(plant-incorporated protectants, or
PIPs). A PIP is defined as ‘‘the pesticidal
substance that is intended to be
produced and used in a living plant and
the genetic material necessary for the
production of such a substance.’’ Many,
but not all, PIPs are exempt from
registration requirements under the
Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA).
CBI is protected by FIFRA and
generally cannot be released to the
public. For most pesticide registration
applications, the current CBI regulations
at 40 CFR part 2 require that claimants
substantiate their CBI claims for their
own records when the claim is made,
and subsequently provide the
substantiation to EPA only if requested.
However, under 40 CFR part 174,
whenever a registrant claims that
information submitted to EPA in
support of a PIP registration application
contains CBI, the registrant must
substantiate such claims to EPA when
they are made. In addition, 40 CFR part
174 also requires manufacturers of PIPs
that are otherwise exempted from
registration requirements to report any
adverse effects of the PIP to the Agency
within 30 days of when the information
is first obtained. Such reporting will
allow the Agency to determine whether
further action is needed to prevent
unreasonable adverse effects to human
health or the environment.
Form Numbers: None.
Respondents/affected entities: Entities
potentially affected by this ICR include
producers and importers of PIPs. The
North American Industrial
Classification System (NAICS) codes for
respondents under this ICR include:
325320 (Pesticide and other Agricultural
Chemical Manufacturing), 325414
(Biological Products (except Diagnostic)
Manufacturing), 422910 (Farm Supplies
Wholesalers), 422930 (Flower, Nursery
Stock, and Florist’s Suppliers), 541710
(Research and Development in the
Physical, Engineering, and Life
Sciences), and 611310 (Colleges,
Universities, and Professional Schools).
Respondent’s obligation to respond:
Mandatory.
Estimated number of respondents: 24
(total).
Frequency of response: On occasion.
Total estimated burden: 518 hours
(per year). Burden is defined at 5 CFR
1320.03(b).
Total estimated cost: $41,892 (per
year), includes $0 annualized capital or
operation and maintenance costs.
Changes in the Estimates: There is an
increase of 86 hours in the total
E:\FR\FM\01JNN1.SGM
01JNN1
Federal Register / Vol. 83, No. 106 / Friday, June 1, 2018 / Notices
estimated respondent burden compared
with the ICR currently approved by
OMB. This increase reflects EPA’s
updating of burden estimates for this
collection based upon historical
information on the number of CBI
substantiations per year. Based upon
revised estimates, the number of CBI
substantiations per year has increased
from 20 to 24, with a corresponding
increase in the associated burden. This
change is an adjustment.
Courtney Kerwin,
Director, Collection Strategies Division.
[FR Doc. 2018–11802 Filed 5–31–18; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2017–0467; FRL–9976–98]
Product Cancellation Order for Certain
Pesticide Registrations and
Amendments To Terminate Uses
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
FOR FURTHER INFORMATION CONTACT:
This notice announces EPA’s
order for the cancellations and
amendments to terminate uses,
voluntarily requested by the registrants
and accepted by the Agency, of the
products listed in Table 1 and Table 2
of Unit II, pursuant to the Federal
Insecticide, Fungicide, and Rodenticide
Act (FIFRA). This cancellation order
follows an October 3, 2017 Federal
Register Notice of Receipt of Requests
from the registrants listed in Table 3 of
Unit II to voluntarily cancel and amend
SUMMARY:
to terminate uses of these product
registrations. In the October 3, 2017
notice, EPA indicated that it would
issue an order implementing the
cancellations and amendments to
terminate uses, unless the Agency
received substantive comments within
the 180-day comment period that would
merit its further review of these
requests, or unless the registrants
withdrew their requests. The Agency
received 5 anonymous public comments
on the notice but none merited its
further review of the requests. Further,
the registrants did not withdraw their
requests. Accordingly, EPA hereby
issues in this notice a cancellation order
granting the requested cancellations and
amendments to terminate uses. Any
distribution, sale, or use of the products
subject to this cancellation order is
permitted only in accordance with the
terms of this order, including any
existing stocks provisions.
DATES: The cancellations and
amendments are applicable June 1,
2018.
Christopher Green, Information
Technology and Resources Management
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
25453
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. 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–2017–0467, is available
at https://www.regulations.gov or at the
Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the
Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton 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
information about the docket available
at https://www.epa.gov/dockets.
II. What action is the Agency taking?
This notice announces the
cancellations and amendments to
terminate uses, as requested by
registrants, of products registered under
FIFRA section 3 (7 U.S.C. 136a).
These registrations are listed in
sequence by registration number in
Tables 1 and 2 of this unit.
TABLE 1—PRODUCT CANCELLATIONS
Registration No.
Company No.
53883–370 .................
CA–130009 ................
WY–080010 ...............
53883
91606
8033
Product name
Active ingredient
Quali-Pro Oxadiazon 50 WSB ...............................
Aspergillus Flavus AF36 ........................................
Assail 70WP Insecticide .........................................
Oxadiazon.
Aspergillus flavus strain AF36.
Acetamiprid.
TABLE 2—PRODUCT REGISTRATION AMENDMENTS TO TERMINATE USES
Registration No.
Company No.
2724
49620–2 .....................
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2724–404 ...................
49620
VerDate Sep<11>2014
17:06 May 31, 2018
Jkt 244001
Product name
Active ingredient
Zoecon RF–322 Ovicidal Pump Spray.
EKA SC–R ....................
PO 00000
Frm 00029
MGK 264; Piperonyl
butoxide; Pyrethrins;
& S-Methoprene.
Sodium chlorate ............
Fmt 4703
Sfmt 4703
Uses to be terminated
Use on horses.
Defoliants/desiccants applied to: Agricultural
drainage systems, beans (dried type), corn,
cotton, fallow land, flax, guar, peas (Southern),
peppers (chili type), potatoes, rice, safflower,
sorghum, soybeans, sunflowers, wheat; and
as an herbicide applied to nonagricultural settings (commercial, industrial, and residential).
E:\FR\FM\01JNN1.SGM
01JNN1
Agencies
[Federal Register Volume 83, Number 106 (Friday, June 1, 2018)]
[Notices]
[Pages 25452-25453]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-11802]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2017-0440; FRL-9978-73-OEI]
Information Collection Request Submitted to OMB for Review and
Approval; Comment Request; Plant-Incorporated Protectants; CBI
Substantiation and Adverse Effects Reporting
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Environmental Protection Agency (EPA) has submitted the
following information collection request (ICR) to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act (PRA): ``Plant-Incorporated Protectants;
CBI Substantiation and Adverse Effects Reporting'' (EPA ICR No.
1693.09, OMB Control No. 2070-0142). This is a request to renew the
approval of an existing ICR, which is currently approved through May
31, 2018. EPA did not receive any public comments in response to the
previously provided public review opportunity issued in the Federal
Register of September 13, 2017. With this submission to OMB, EPA is
providing an additional 30 days for public review and comment. 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 July 2, 2018.
ADDRESSES: Submit your comments, identified by Docket ID number EPA-HQ-
OPP-2017-0440, to both EPA and OMB as follows:
To EPA online using https://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, and
To OMB via email to [email protected]. Address
comments to the OMB Desk Officer for EPA.
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.
FOR FURTHER INFORMATION CONTACT: Ryne Yarger, Field and External
Affairs Division, 7506P, Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC 20460; telephone number: 703-605-
1193; fax number: 703-305-5884; email address: [email protected].
SUPPLEMENTARY INFORMATION:
Docket: Supporting documents, including the ICR that explains in
detail the information collection activities and the related burden and
cost estimates that are summarized in this document, are available in
the docket for this ICR. The docket can be viewed online at https://www.regulations.gov or in person at the EPA Docket Center, West William
Jefferson Clinton Bldg., Rm. 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: This ICR addresses the two information collection
requirements contained in the regulations codified in 40 CFR part 174
pertaining to pesticidal substances that are produced by plants (plant-
incorporated protectants, or PIPs). A PIP is defined as ``the
pesticidal substance that is intended to be produced and used in a
living plant and the genetic material necessary for the production of
such a substance.'' Many, but not all, PIPs are exempt from
registration requirements under the Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA).
CBI is protected by FIFRA and generally cannot be released to the
public. For most pesticide registration applications, the current CBI
regulations at 40 CFR part 2 require that claimants substantiate their
CBI claims for their own records when the claim is made, and
subsequently provide the substantiation to EPA only if requested.
However, under 40 CFR part 174, whenever a registrant claims that
information submitted to EPA in support of a PIP registration
application contains CBI, the registrant must substantiate such claims
to EPA when they are made. In addition, 40 CFR part 174 also requires
manufacturers of PIPs that are otherwise exempted from registration
requirements to report any adverse effects of the PIP to the Agency
within 30 days of when the information is first obtained. Such
reporting will allow the Agency to determine whether further action is
needed to prevent unreasonable adverse effects to human health or the
environment.
Form Numbers: None.
Respondents/affected entities: Entities potentially affected by
this ICR include producers and importers of PIPs. The North American
Industrial Classification System (NAICS) codes for respondents under
this ICR include: 325320 (Pesticide and other Agricultural Chemical
Manufacturing), 325414 (Biological Products (except Diagnostic)
Manufacturing), 422910 (Farm Supplies Wholesalers), 422930 (Flower,
Nursery Stock, and Florist's Suppliers), 541710 (Research and
Development in the Physical, Engineering, and Life Sciences), and
611310 (Colleges, Universities, and Professional Schools).
Respondent's obligation to respond: Mandatory.
Estimated number of respondents: 24 (total).
Frequency of response: On occasion.
Total estimated burden: 518 hours (per year). Burden is defined at
5 CFR 1320.03(b).
Total estimated cost: $41,892 (per year), includes $0 annualized
capital or operation and maintenance costs.
Changes in the Estimates: There is an increase of 86 hours in the
total
[[Page 25453]]
estimated respondent burden compared with the ICR currently approved by
OMB. This increase reflects EPA's updating of burden estimates for this
collection based upon historical information on the number of CBI
substantiations per year. Based upon revised estimates, the number of
CBI substantiations per year has increased from 20 to 24, with a
corresponding increase in the associated burden. This change is an
adjustment.
Courtney Kerwin,
Director, Collection Strategies Division.
[FR Doc. 2018-11802 Filed 5-31-18; 8:45 am]
BILLING CODE 6560-50-P