Flubendiamide; Pesticide Tolerances, 30979-30982 [2017-14108]
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30979
Federal Register / Vol. 82, No. 127 / Wednesday, July 5, 2017 / Rules and Regulations
EPA-APPROVED KENTUCKY NON-REGULATORY PROVISIONS—Continued
State
submittal date/
effective date
Name of non-regulatory SIP
provision
Applicable geographic or nonattainment area
2008 8-hour ozone base year
emissions inventory for the
Kentucky portion of the Cincinnati-Hamilton, OH-KY-IN
Area.
Portions of Boone, Campbell and Kenton Counties in Kentucky.
PART 81—DESIGNATION OF AREAS
FOR AIR QUALITY PLANNING
PURPOSES
3. The authority citation for part 81
continues to read as follows:
■
EPA approval
date
8/26/2016
Authority: 42 U.S.C. 7401 et seq.
7/5/2017 .........
[Insert citation
of publication].
Explanations
182(a)(1)
base-year
emissions
inventory
by revising the entries for ‘‘Cincinnati,
OH-KY-IN’’ to read as follows:
4. In § 81.318, the table entitled
‘‘Kentucky-2008 8-Hour Ozone NAAQS
(Primary and secondary)’’ is amended
■
§ 81.318
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Kentucky.
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KENTUCKY—2008 8-HOUR OZONE NAAQS
[Primary and secondary]
Designation
Classification
Designated area
Date 1
Cincinnati, OH-KY-IN: 2
Boone County (part) ...................................................................................
2000 Census tracts: 702, 703.05, 703.06, 703.07, 703.08, 703.09,
704.01, 704.02, 705.01, 705.02, 706.01, 706.03, 706.04.
Campbell County (part) ..............................................................................
2000 Census tracts: 501, 502, 503, 504, 505, 506, 512, 513,
519.01, 519.03, 519.04, 520.01, 520.02, 521, 522, 523.01,
523.02, 524, 525, 526, 528, 529, 530, 531.
Kenton County (part) ..................................................................................
2000 Census tracts: 603, 607, 609, 610, 611, 612, 613, 614, 616,
636.03, 636.04, 636.05, 636.06, 638, 640, 641, 642, 643, 644,
645, 646, 647, 648, 649, 650, 651, 652, 653, 654, 655.01,
655.02, 656, 657, 658, 659, 668, 669, 670, 671.
Date 1
Type
7/5/2017
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Attainment.
Attainment.
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Attainment.
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Type
Attainment.
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date is July 20, 2012, unless otherwise noted.
2 Excludes Indian country located in each area, unless otherwise noted.
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[FR Doc. 2017–13994 Filed 7–3–17; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2007–0099; FRL–9962–13]
Flubendiamide; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes a
tolerance for residues of flubendiamide
in or on tea at 50 parts per million
(ppm). Nichino America, Inc. requested
this tolerance under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective July
5, 2017. Objections and requests for
hearings must be received on or before
September 5, 2017, and must be filed in
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SUMMARY:
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accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
ADDRESSES: The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2007–0099, 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.
FOR FURTHER INFORMATION CONTACT:
Michael L. Goodis, P.E., Director,
PO 00000
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Fmt 4700
Sfmt 4700
Registration Division (7505P), Office of
Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW., Washington, DC 20460–0001;
main telephone number: (703) 305–
7090; email address: RDFRNotices@
epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
E:\FR\FM\05JYR1.SGM
05JYR1
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Federal Register / Vol. 82, No. 127 / Wednesday, July 5, 2017 / Rules and Regulations
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
sradovich on DSK3GMQ082PROD with RULES
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Printing Office’s e-CFR
site at https://www.ecfr.gov/cgi-bin/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl.
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2007–0099 in the subject line on
the first page of your submission. All
objections and requests for a hearing
must be in writing, and must be
received by the Hearing Clerk on or
before September 5, 2017. Addresses for
mail and hand delivery of objections
and hearing requests are provided in 40
CFR 178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
disclosed publicly by EPA without prior
notice. Submit the non-CBI copy of your
objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2007–0099, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be CBI or
other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW., Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on commenting
or visiting the docket, along with more
information about dockets generally, is
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16:11 Jul 03, 2017
Jkt 241001
available at https://www.epa.gov/
dockets.
II. Summary of Petitioned-For
Tolerance
In the Federal Register of August 12,
2016 (81 FR 53379) (FRL–9949–53),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announced the filing of a
pesticide petition (PP 6E8463) by
Nichino America, Inc., 4550 New
Linden Hill Road, Suite 501,
Wilmington, DE 19808–2951. This
petition requested that 40 CFR 180.639
be amended by establishing an import
tolerance for residues of flubendiamide,
N2-[1,1-dimethyl-2(methylsulfonyl)ethyl-3-iodo-N1-[2methyl-4-[1,2,2,2-tetrafluoro-1(trifluoromethyl)ethyl]phenyl]-1,2benzenedicarboxamide, in or on the
processed commodity of dried tea at 60
parts per million (ppm). This document
referenced a summary of a petition
prepared by Nichino America, Inc., the
registrant, which is available in the
docket, https://www.regulations.gov.
This tolerance was requested to cover
residues of flubendiamide in or on tea
resulting from uses of this pesticide on
tea outside the United States; there is no
current U.S. registration for use of
flubendiamide on tea. In order to
harmonize with Codex, EPA is
establishing a tolerance for residues of
flubendiamide in or on tea at 50 ppm.
The available residue data supports this
tolerance level. A revised Section F was
submitted by Nichino America, Inc. to
support this change to the petitioned-for
tolerance. There were no comments
received in response to the notice of
filing.
III. Aggregate Risk Assessment and
Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA
allows EPA to establish a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(b)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings, but does not include
occupational exposure. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing a
tolerance and to ‘‘ensure that there is a
reasonable certainty that no harm will
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result to infants and children from
aggregate exposure to the pesticide
chemical residue. . . .’’
Consistent with FFDCA section
408(b)(2)(D), and the factors specified in
FFDCA section 408(b)(2)(D), EPA has
reviewed the available scientific data
and other relevant information in
support of this action. EPA has
sufficient data to assess the hazards of
and to make a determination on
aggregate exposure for flubendiamide
including exposure resulting from the
tolerance established by this action.
In the Federal Register of December
12, 2012 (77 FR 73940) (FRL–9373–3),
EPA amended tolerances for residues of
flubendiamide in or on apple, wet
pomace and fruit, pome, group 11. EPA
is relying upon significant portions of
those risk assessments and the
corresponding findings made in the
December 12, 2012 Federal Register
document in support of this action for
the following reasons. The toxicity
profile of flubendiamide has not
changed. Much of the exposure profiled
remains the same as well because there
is no U.S. registration associated with
the tea use (i.e., the estimated drinking
water exposures reported in 2012 are
not expected to change nor is there any
need to conduct a residential exposure
assessment due to the lack of proposed
or existing residential uses for
flubendiamide). The Agency did take
into consideration the potential
additional dietary exposure to
flubendiamide as a result of residues in
or on imported tea. Aggregating that
exposure with the dietary exposure
estimated in the December 2012
tolerance assessment resulted in no
change to the acute dietary exposure
(3.1% of the aPAD for the general U.S.
population and 5.5% of the aPAD for
children 1–2 years old, the most highly
exposed population subgroup) and only
a 1% change in the chronic dietary risk
(21% of the cPAD) for the general U.S.
population and an increase of 9% in the
chronic dietary risk (67% of the cPAD)
for children 1–2 years old, the most
highly exposed population subgroup.
The Agency’s findings concerning
cumulative effects and the children’s
safety factor as reflected in the
December 2012 tolerance rulemaking
are also relied upon in this action.
Based upon the risk assessments
supporting the December 12, 2012
Federal Register document, the findings
therein, and the updated risk
assessment accounting for the residues
of flubendiamide on imported tea, EPA
concludes that there is a reasonable
certainty that no harm will result to the
general population, or to infants and
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children from aggregate exposure to
flubendiamide residues.
For a detailed discussion of the
aggregate risk assessments and
determination of safety for these
tolerances, please refer to the December
12, 2012, Federal Register document
and its supporting documents, available
at https://www.regulations.gov in docket
ID number EPA–HQ–OPP–2007–0099.
Further information about EPA’s
determination that an updated risk
assessment was not necessary may be
found in the document,
‘‘Flubendiamide: Human Health Risk
Assessment for the Petition for a
Tolerance Without U.S. Registration for
Residues in/on Tea.’’ in docket ID
number EPA–HQ–OPP–2007–0099.
IV. Other Considerations
A. Analytical Enforcement Methodology
An independently validated liquid
chromatography/tandem mass
spectrometry (LC/MS/MS) method,
Method 00816/M002, was previously
submitted for the determination of
residues of in/on samples of plant
commodities. The validated limit of
quantitation (LOQ) is 0.01 ppm for each
analyte in each matrix.
B. International Residue Limits
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In making its tolerance decisions, EPA
seeks to harmonize U.S. tolerances with
international standards whenever
possible, consistent with U.S. food
safety standards and agricultural
practices. EPA considers the
international maximum residue limits
(MRLs) established by the Codex
Alimentarius Commission (Codex), as
required by FFDCA section 408(b)(4).
The Codex Alimentarius is a joint
United Nations Food and Agriculture
Organization/World Health
Organization food standards program,
and it is recognized as an international
food safety standards-setting
organization in trade agreements to
which the United States is a party. EPA
may establish a tolerance that is
different from a Codex MRL; however,
FFDCA section 408(b)(4) requires that
EPA explain the reasons for departing
from the Codex level. There is currently
a Codex MRL for tea established at 50
ppm; therefore, the U.S. EPA is
establishing a tolerance on tea at the
same level to harmonize with Codex.
C. Revisions to Petitioned-For Tolerance
If only dried tea data are submitted for
imported tea (data in/on the RAC are
not required for imported tea) and the
tolerance level based on these data is
also meant to cover for detectable
residues in instant tea (may be
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demonstrated by data depicting
detectable residues in brewed tea), then
the correct commodity definition for
tolerance setting should be ‘‘tea’’ to
cover incurred residues in or on all tea
commodities and eliminate any
regulatory ambiguity. In order to
harmonize with Codex, EPA is
establishing a tolerance for residues of
flubendiamide in or on tea at 50 ppm.
The available residue data supports this
tolerance level. A revised Section F was
submitted by Nichino America, Inc. to
support this change to the petitioned-for
tolerance.
V. Conclusion
Therefore, a tolerance is established
for residues of flubendiamide, N2-[1,1dimethyl-2-(methylsulfonyl)ethyl-3iodo-N1-[2-methyl-4-[1,2,2,2-tetrafluoro1-(trifluoromethyl)ethyl]phenyl]-1,2benzenedicarboxamide, in or on tea at
50 ppm. At this time, there is no U.S.
registration for use of flubendiamide on
tea.
VI. Statutory and Executive Order
Reviews
This action establishes a tolerance
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997). This action does not
contain any information collections
subject to OMB approval under the
Paperwork Reduction Act (PRA) (44
U.S.C. 3501 et seq.), nor does it require
any special considerations under
Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerance in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
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30981
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
has determined that this action will not
have a substantial direct effect on States
or tribal governments, on the
relationship between the national
government and the States or tribal
governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, the Agency has determined
that Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999) and Executive Order 13175,
entitled ‘‘Consultation and Coordination
with Indian Tribal Governments’’ (65 FR
67249, November 9, 2000) do not apply
to this action. In addition, this action
does not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act (UMRA) (2 U.S.C.
1501 et seq.).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: May 23, 2017.
Donna S. Davis,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
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Federal Register / Vol. 82, No. 127 / Wednesday, July 5, 2017 / Rules and Regulations
2. In § 180.639, add alphabetically the
entry ‘‘Tea’’ to the table in paragraph (a)
to read as follows:
■
§ 180.639 Flubendiamide; tolerances for
residues.
(a) * * *
(1) * * *
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Tea 1 ......................................
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50
*
*
1 There are no U.S. registrations as of July
5, 2017, for use of flubendiamide on tea.
*
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[FR Doc. 2017–14108 Filed 7–3–17; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2016–0166; FRL–9962–61]
Indaziflam; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
tolerances for residues of indaziflam in
or on multiple commodities which are
identified and discussed later in this
document. Interregional Research
Project Number 4 (IR–4) requested these
tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective July
5, 2017. Objections and requests for
hearings must be received on or before
September 5, 2017, and must be filed in
accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
ADDRESSES: The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2016–0166, 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.
sradovich on DSK3GMQ082PROD with RULES
SUMMARY:
VerDate Sep<11>2014
16:11 Jul 03, 2017
Jkt 241001
FOR FURTHER INFORMATION CONTACT:
Michael Goodis, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
DC 20460–0001; main telephone
number: (703) 305–7090; email address:
RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Printing Office’s e-CFR
site at https://www.ecfr.gov/cgi-bin/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl.
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2016–0166 in the subject line on
the first page of your submission. All
objections and requests for a hearing
must be in writing, and must be
received by the Hearing Clerk on or
before September 5, 2017. Addresses for
mail and hand delivery of objections
and hearing requests are provided in 40
CFR 178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
PO 00000
Frm 00036
Fmt 4700
Sfmt 4700
Information not marked confidential
pursuant to 40 CFR part 2 may be
disclosed publicly by EPA without prior
notice. Submit the non-CBI copy of your
objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2016–0166, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be CBI or
other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW., Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
II. Summary of Petitioned-For
Tolerance
In the Federal Register of May 19,
2016 (81 FR 31581) (FRL–9946–02),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide petition (PP 6E8452) by IR–4,
Rutgers University, 500 College Rd.
East, Suite 201 W, Princeton, NJ 08540.
The petition requested that 40 CFR
180.653 be amended by establishing
tolerances for residues of the herbicide
indaziflam (N-[(1R,2S)-2,3-dihydro-2,6dimethyl-1H-inden-1-yl]-6-(1fluoroethyl)-1,3,5-triazine-2,4-diamine)
in or on bushberry, subgroup 13–07B at
0.01 parts per million (ppm); caneberry,
subgroup 13–07A at 0.01 ppm; coffee,
green bean at 0.01 ppm; fruit, small,
vine climbing, except fuzzy kiwifruit,
subgroup 13–07F at 0.01 ppm; hop,
dried cones at 0.03 ppm; fruit, stone,
group 12–12 at 0.01 ppm; and nut, tree,
group 14–12 at 0.01 ppm. Additionally,
the petition requested that tolerances be
established for the crops in the
proposed crop subgroup 23A (small
fruit, edible peel subgroup) at 0.01 ppm,
including acerola; African plum; agritos,
almondette; appleberry; arbutus berry;
bayberry, red; bignay; breadnut;
cabeluda; carandas-plum; Ceylon iron
wood; Ceylon olive; cherry-of-the-RioGrande; Chinese olive, black; Chinese
olive, white; chirauli-nut; cocoplum;
desert-date; false sandalwood; fragrant
manjack; gooseberry, Abyssinian;
gooseberry, Ceylon; gooseberry,
E:\FR\FM\05JYR1.SGM
05JYR1
Agencies
[Federal Register Volume 82, Number 127 (Wednesday, July 5, 2017)]
[Rules and Regulations]
[Pages 30979-30982]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-14108]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2007-0099; FRL-9962-13]
Flubendiamide; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes a tolerance for residues of
flubendiamide in or on tea at 50 parts per million (ppm). Nichino
America, Inc. requested this tolerance under the Federal Food, Drug,
and Cosmetic Act (FFDCA).
DATES: This regulation is effective July 5, 2017. Objections and
requests for hearings must be received on or before September 5, 2017,
and must be filed in accordance with the instructions provided in 40
CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2007-0099, 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.
FOR FURTHER INFORMATION CONTACT: Michael L. Goodis, P.E., Director,
Registration Division (7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460-0001; main telephone number: (703) 305-7090; email
address: RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
[[Page 30980]]
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of EPA's
tolerance regulations at 40 CFR part 180 through the Government
Printing Office's e-CFR site at https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, any person may file an
objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2007-0099 in the subject line on the first
page of your submission. All objections and requests for a hearing must
be in writing, and must be received by the Hearing Clerk on or before
September 5, 2017. Addresses for mail and hand delivery of objections
and hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be disclosed publicly by EPA without
prior notice. Submit the non-CBI copy of your objection or hearing
request, identified by docket ID number EPA-HQ-OPP-2007-0099, by one of
the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be CBI or other
information whose disclosure is restricted by statute.
Mail: OPP Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html. Additional
instructions on commenting or visiting the docket, along with more
information about dockets generally, is available at https://www.epa.gov/dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of August 12, 2016 (81 FR 53379) (FRL-9949-
53), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announced the filing of a pesticide petition (PP
6E8463) by Nichino America, Inc., 4550 New Linden Hill Road, Suite 501,
Wilmington, DE 19808-2951. This petition requested that 40 CFR 180.639
be amended by establishing an import tolerance for residues of
flubendiamide, N\2\-[1,1-dimethyl-2-(methylsulfonyl)ethyl-3-iodo-N\1\-
[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-1,2-
benzenedicarboxamide, in or on the processed commodity of dried tea at
60 parts per million (ppm). This document referenced a summary of a
petition prepared by Nichino America, Inc., the registrant, which is
available in the docket, https://www.regulations.gov. This tolerance was
requested to cover residues of flubendiamide in or on tea resulting
from uses of this pesticide on tea outside the United States; there is
no current U.S. registration for use of flubendiamide on tea. In order
to harmonize with Codex, EPA is establishing a tolerance for residues
of flubendiamide in or on tea at 50 ppm. The available residue data
supports this tolerance level. A revised Section F was submitted by
Nichino America, Inc. to support this change to the petitioned-for
tolerance. There were no comments received in response to the notice of
filing.
III. Aggregate Risk Assessment and Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a
tolerance (the legal limit for a pesticide chemical residue in or on a
food) only if EPA determines that the tolerance is ``safe.'' Section
408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a
reasonable certainty that no harm will result from aggregate exposure
to the pesticide chemical residue, including all anticipated dietary
exposures and all other exposures for which there is reliable
information.'' This includes exposure through drinking water and in
residential settings, but does not include occupational exposure.
Section 408(b)(2)(C) of FFDCA requires EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance and to ``ensure that there
is a reasonable certainty that no harm will result to infants and
children from aggregate exposure to the pesticide chemical residue. . .
.''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified in FFDCA section 408(b)(2)(D), EPA has reviewed the available
scientific data and other relevant information in support of this
action. EPA has sufficient data to assess the hazards of and to make a
determination on aggregate exposure for flubendiamide including
exposure resulting from the tolerance established by this action.
In the Federal Register of December 12, 2012 (77 FR 73940) (FRL-
9373-3), EPA amended tolerances for residues of flubendiamide in or on
apple, wet pomace and fruit, pome, group 11. EPA is relying upon
significant portions of those risk assessments and the corresponding
findings made in the December 12, 2012 Federal Register document in
support of this action for the following reasons. The toxicity profile
of flubendiamide has not changed. Much of the exposure profiled remains
the same as well because there is no U.S. registration associated with
the tea use (i.e., the estimated drinking water exposures reported in
2012 are not expected to change nor is there any need to conduct a
residential exposure assessment due to the lack of proposed or existing
residential uses for flubendiamide). The Agency did take into
consideration the potential additional dietary exposure to
flubendiamide as a result of residues in or on imported tea.
Aggregating that exposure with the dietary exposure estimated in the
December 2012 tolerance assessment resulted in no change to the acute
dietary exposure (3.1% of the aPAD for the general U.S. population and
5.5% of the aPAD for children 1-2 years old, the most highly exposed
population subgroup) and only a 1% change in the chronic dietary risk
(21% of the cPAD) for the general U.S. population and an increase of 9%
in the chronic dietary risk (67% of the cPAD) for children 1-2 years
old, the most highly exposed population subgroup. The Agency's findings
concerning cumulative effects and the children's safety factor as
reflected in the December 2012 tolerance rulemaking are also relied
upon in this action.
Based upon the risk assessments supporting the December 12, 2012
Federal Register document, the findings therein, and the updated risk
assessment accounting for the residues of flubendiamide on imported
tea, EPA concludes that there is a reasonable certainty that no harm
will result to the general population, or to infants and
[[Page 30981]]
children from aggregate exposure to flubendiamide residues.
For a detailed discussion of the aggregate risk assessments and
determination of safety for these tolerances, please refer to the
December 12, 2012, Federal Register document and its supporting
documents, available at https://www.regulations.gov in docket ID number
EPA-HQ-OPP-2007-0099. Further information about EPA's determination
that an updated risk assessment was not necessary may be found in the
document, ``Flubendiamide: Human Health Risk Assessment for the
Petition for a Tolerance Without U.S. Registration for Residues in/on
Tea.'' in docket ID number EPA-HQ-OPP-2007-0099.
IV. Other Considerations
A. Analytical Enforcement Methodology
An independently validated liquid chromatography/tandem mass
spectrometry (LC/MS/MS) method, Method 00816/M002, was previously
submitted for the determination of residues of in/on samples of plant
commodities. The validated limit of quantitation (LOQ) is 0.01 ppm for
each analyte in each matrix.
B. International Residue Limits
In making its tolerance decisions, EPA seeks to harmonize U.S.
tolerances with international standards whenever possible, consistent
with U.S. food safety standards and agricultural practices. EPA
considers the international maximum residue limits (MRLs) established
by the Codex Alimentarius Commission (Codex), as required by FFDCA
section 408(b)(4). The Codex Alimentarius is a joint United Nations
Food and Agriculture Organization/World Health Organization food
standards program, and it is recognized as an international food safety
standards-setting organization in trade agreements to which the United
States is a party. EPA may establish a tolerance that is different from
a Codex MRL; however, FFDCA section 408(b)(4) requires that EPA explain
the reasons for departing from the Codex level. There is currently a
Codex MRL for tea established at 50 ppm; therefore, the U.S. EPA is
establishing a tolerance on tea at the same level to harmonize with
Codex.
C. Revisions to Petitioned-For Tolerance
If only dried tea data are submitted for imported tea (data in/on
the RAC are not required for imported tea) and the tolerance level
based on these data is also meant to cover for detectable residues in
instant tea (may be demonstrated by data depicting detectable residues
in brewed tea), then the correct commodity definition for tolerance
setting should be ``tea'' to cover incurred residues in or on all tea
commodities and eliminate any regulatory ambiguity. In order to
harmonize with Codex, EPA is establishing a tolerance for residues of
flubendiamide in or on tea at 50 ppm. The available residue data
supports this tolerance level. A revised Section F was submitted by
Nichino America, Inc. to support this change to the petitioned-for
tolerance.
V. Conclusion
Therefore, a tolerance is established for residues of
flubendiamide, N\2\-[1,1-dimethyl-2-(methylsulfonyl)ethyl-3-iodo-N\1\-
[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-1,2-
benzenedicarboxamide, in or on tea at 50 ppm. At this time, there is no
U.S. registration for use of flubendiamide on tea.
VI. Statutory and Executive Order Reviews
This action establishes a tolerance under FFDCA section 408(d) in
response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001) or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997). This action does not contain any
information collections subject to OMB approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et seq.), nor does it require any
special considerations under Executive Order 12898, entitled ``Federal
Actions to Address Environmental Justice in Minority Populations and
Low-Income Populations'' (59 FR 7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerance in this
final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
tribal governments, on the relationship between the national government
and the States or tribal governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian tribes. Thus, the Agency has
determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999) and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November 9, 2000) do not apply to this action. In addition, this
action does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
(UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: May 23, 2017.
Donna S. Davis,
Acting Director, Registration Division, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
[[Page 30982]]
0
2. In Sec. 180.639, add alphabetically the entry ``Tea'' to the table
in paragraph (a) to read as follows:
Sec. 180.639 Flubendiamide; tolerances for residues.
(a) * * *
(1) * * *
* * * * *
Tea \1\................................................. 50
* * * * *
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\1\ There are no U.S. registrations as of July 5, 2017, for use of
flubendiamide on tea.
* * * * *
[FR Doc. 2017-14108 Filed 7-3-17; 8:45 am]
BILLING CODE 6560-50-P