Flutianil; Pesticide Tolerances, 12265-12269 [2018-05640]
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12265
Federal Register / Vol. 83, No. 55 / Wednesday, March 21, 2018 / Rules and Regulations
germane to this action; therefore, no
further response from the Agency is
required.
sradovich on DSK3GMQ082PROD with RULES
V. Conclusion
Therefore, tolerances are amended for
residues of aluminum tris (Oethylphosphonate), in or on fruit, citrus,
group 10–10 at 9.0 ppm.
VI. Statutory and Executive Order
Reviews
This action amends and expands an
existing crop group 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
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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: March 7, 2018.
Michael Goodis,
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.
2. In § 180.415,
a. Remove the entry for ‘‘Fruit, citrus,
group 10’’ from the table in paragraph
(a).
■ b. Add alphabetically an entry to the
table in paragraph (a) for ‘‘Fruit, citrus,
group 10–10’’.
The addition reads as follows:
■
■
§ 180.415 Aluminum tris (Oethylphosphonate); tolerances for residues.
(a) *
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Parts per
million
Commodity
*
*
*
*
Fruit, citrus, group 10–10 .............
*
*
*
*
*
*
*
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*
9.0
*
*
[FR Doc. 2018–05642 Filed 3–20–18; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2015–0817; FRL–9974–32]
Flutianil; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
tolerances for residues of flutianil in or
on multiple commodities that are
identified and discussed later in this
document and an exemption for indirect
or inadvertent residues of flutianil on
other crops rotated into fields
previously treated with flutianil. OAT
AGRIO Company, Ltd. requested these
tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective
March 21, 2018. Objections and requests
for hearings must be received on or
before May 21, 2018, 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–2015–0817, 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, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
SUMMARY:
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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.
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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–2015–0817 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 May 21, 2018. 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
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objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2015–0817, 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 April 25,
2016 (81 FR 24044) (FRL–9944–86),
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 5F8408) by OAT
AGRIO Company, Ltd, 1–3–1 Kanda
Ogawa-machi, Chiyoda-ku, Tokyo 101–
0052, Japan. The petition requested that
40 CFR part 180 be amended by
establishing tolerances for residues of
the fungicide flutianil, (2Z)-2-[2-fluoro5-(trifluoromethyl)phenyl]sulfanyl-2-[3(2-methoxyphenyl)thiazolidin-2ylidene]acetonitrile, in or on apple, fruit
at 0.2 parts per million (ppm); apple,
juice at 0.03 ppm; apple, wet pomace at
2 ppm; cantaloupe at 0.07 ppm; cherry,
fruit at 0.4 ppm; cucumber at 0.02 ppm;
grape, fruit at 0.7 ppm; grape, juice at
0.2 ppm; grape, raisins at 0.3 ppm;
squash at 0.03 ppm; and strawberry,
fruit at 0.3 ppm. That document
referenced a summary of the petition
prepared by OAT AGRIO Company Ltd.,
the registrant, which is available in the
docket, https://www.regulations.gov. One
comment was received on the notice of
filing. EPA’s response to this comments
is discussed in Unit IV.C.
Following the publication of this
notice, the petitioner revised its petition
by revising commodity terms to be
consistent with the terminology EPA
uses for commodities, removing certain
processed commodities for which
specific tolerances are not needed,
amending tolerance levels, and
requesting an exemption to cover
inadvertent residues. EPA published a
notice in the Federal Register of
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October 12, 2017 (82 FR 47422) (FRL–
9967–09), pursuant to FFDCA section
408(d)(3), 21 U.S.C. 346a(d)(3),
announcing OAT AGRIO Company’s
amended pesticide petition (PP 5F8408).
Superseding the original petition, the
revised petition requested that 40 CFR
part 180 be amended by establishing
tolerances for residues of the fungicide
flutianil in or on apple at 0.15 parts per
million (ppm); apple, wet pomace at
0.30 ppm; cantaloupe at 0.07 ppm;
cherry at 0.40 ppm; cucumber at 0.20;
ppm; grape at 0.70 ppm; squash at 0.05
ppm; and strawberry at 0.50 ppm.
Additionally, OAT AGRIO Company
requested that an exemption from the
requirement of a tolerance be
established in 40 CFR 180 for indirect
or inadvertent residues of fungicide,
flutianil in or on all food commodities
for which tolerances are not separately
established. Comments were received
on the notice of filing. EPA’s response
to these comments is discussed in Unit
IV.C.
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. . . .’’
Similarly, FFDCA section 408(c)(2)
authorizes EPA to establish an
exemption from the requirement of a
tolerance only if EPA determines the
exemption is ‘‘safe’’, which has the
same definition for exemptions as for
tolerances and requires consideration of
the same exposures and factors as for
tolerances. 21 U.S.C. 346a(c)(2)(B).
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
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sufficient data to assess the hazards of
and to make a determination on
aggregate exposure for flutianil
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with flutianil follows.
EPA has evaluated the available
toxicity data and considered its validity,
completeness, and reliability as well as
the relationship of the results of the
studies to human risk. EPA has also
considered available information
concerning the variability of the
sensitivities of major identifiable
subgroups of consumers, including
infants and children.
No single or repeated dose study
performed by any route of exposure
produced an adverse effect following
flutianil exposure below, at, or above
the limit dose (1,000 mg/kg/day). The
only toxic effect of flutianil exposure in
the rat 28-day, 90-day, or 104-day oral
toxicity studies was associated with
hyaline droplet formation in the renal
proximal tubular cells of males. No
toxicity was observed in the female rats
dosed up to the limit dose for
comparable time periods. An
immunohistochemical staining
demonstrated that the hyaline droplets
in the proximal tubular cells were
related to the presence of alpha-2mglobulin, which is not relevant for
human toxicity. Based on the link to
alpha-2m-globulin and the lack of any
degenerative or other associated effects,
the hyaline droplet was not considered
biologically relevant to humans.
No toxicity was seen in the
developmental, reproductive,
neurotoxic, or immunotoxic studies for
flutianil. No dermal or systemic toxicity
was observed at the limit dose in the rat
28-day dermal toxicity study.
Nevertheless, in the rat 28-day
inhalation toxicity study, increased lung
weights in females and
histopathological findings of minimal
nasal mucous cell hypertrophy/
hyperplasia and minimal lung
centriacinar inflammation in males and
females were observed at the highest
dose tested. These observations were
consistent with response to aerosol
exposure to an airway irritant. The nasal
mucous cell hypertrophy/hyperplasia is
considered the physiological response
of these cells to irritant; however, the
increased lung weights and cellular
inflammation reflect some degree of
edema in air spaces, and inflammation
in the lung could affect airway
responsiveness and pulmonary
function. Therefore, the increased lung
weights in females and lung lesions in
both sexes were considered adverse
effects. Flutianil is classified as ‘‘Not
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Likely to be Carcinogenic to Humans’’
based on lack of evidence of
carcinogenicity in rats and mice and no
evidence of mutagenicity. Flutianil
produced no genotoxicity.
Specific information on the studies
received and the nature of the adverse
effects caused by flutianil as well as the
no-observed-adverse-effect-level
(NOAEL) and the lowest-observedadverse-effect-level (LOAEL) from the
toxicity studies can be found at https://
www.regulations.gov in document
‘‘Flutianil. Draft Human Risk
Assessment to Support New Uses for a
New Active Ingredient, Flutianil on
Apple, Cantaloupe, Cherry, Cucumber,
Grape, Summer Squash, and
Strawberry’’ dated November 1, 2017 in
docket ID number EPA–HQ–OPP–2015–
0817.
Based on the analysis of the available
flutianil toxicological studies, there is
no adverse toxicity from oral exposures
seen in any of the required submitted
toxicology studies. No toxicity endpoint
and point of departure for regulating
dietary exposure is established for the
human health risk assessment. There are
no registered or proposed residential
uses at this time for flutianil; therefore,
residential handler and post-application
exposure and risk were not assessed.
Flutianil is proposed for use on a
variety of crops. Humans could
potentially be exposed to flutianil
residues in food because flutianil may
be applied directly to growing crops.
These applications can also result in
flutianil reaching surface and ground
water, both of which can serve as
sources of drinking water. There are no
proposed uses in residential settings;
therefore, there are no anticipated
residential exposures.
Based on the toxicological profile of
flutianil, EPA has concluded that the
FFDCA requirements to retain an
additional safety factor for protection of
infants and children and to consider
cumulative effects do not apply. Section
408(b)(2)(C) of the FFDCA (21 U.S.C.
346a) requires an additional tenfold
margin of safety in the case of threshold
risks, which are not present in this case.
Section 408(b)(2)(D)(v) of the FFDCA
requires consideration of information
concerning cumulative effects of
substances that have a common
mechanism of toxicity, which flutianil
does not have.
Based on the available data indicating
a lack of adverse effects from exposure
to flutianil, EPA concludes that there is
a reasonable certainty that no harm will
result to the general population, or to
infants and children from aggregate
exposure to flutianil.
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IV. Other Considerations
A. Analytical Enforcement Methodology
The gas chromatography-mass
spectrometry detector (GC/MSD) is used
to measure and evaluate the chemical
flutianil on apples, cantaloupe, cherry,
cucumber, squash, and strawberry. The
high performance liquid
chromatography with tandem mass
spectral detection (LCMS/MS) is used to
measure and evaluate the chemical
flutianil and the metabolite OC–56635
in grapes.
Adequate enforcement methodology
(gas chromatography) is available to
enforce the tolerance expression.
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.
The Codex has not established a MRL
for flutianil.
C. Response to Comments
Several comments were received,
although many simply expressed
concern about the use of pesticides on
food generally. While EPA recognizes
that some individuals oppose the use of
pesticides in or on food, the FFDCA
authorizes EPA to establish tolerances
or exemptions where it determines that
doing so is safe. As required by the
FFDCA, EPA conducted a
comprehensive assessment of flutianil,
including its potential for
carcinogenicity. Based on its assessment
of the available data, the Agency
believes that given the observed lack of
toxicity of this chemical, no risks of
concern are expected. Therefore, EPA
concludes that the tolerances and
exemption are safe and can be
supported. The commenters did not
provide any information to indicate
otherwise.
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Some comments (i.e., comments from
the Center for Biological Diversity
(CBD)) were not relevant to this action
because they raised issues concerning
compliance with the Endangered
Species Act (ESA) and the Federal
Insecticide, Fungicide, and Rodenticide
Act (FIFRA), which is not relevant to
the determination needed to support
tolerance actions under the FFDCA.
Comments were received on the
potential of flutianil to harm humans
based on the human health and
environmental toxicity findings of the
European Food Safety Authority
(EFSA). Although concerns were raised
in the EFSA report about the potential
for carcinogenicity and reproductive
toxicity of flutianil, EPA has received
additional data on flutianil supporting
the Agency’s conclusions of a lack of
carcinogenicity or reproductive toxicity.
Therefore, EPA concludes that it has
sufficient data to address the concerns
raised by the EFSA assessment and
support its safety finding for flutianil.
For further information concerning
these studies, see the ‘‘Final Registration
Decision for the New Active Ingredient
Flutianil: A Fungicide for Use on
Apples, Cantaloupes, Cherries,
Cucumbers, Grapes, Squash, and
Strawberries’’ [Docket ID Number EPA–
HQ–OPP–2015–0817].
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V. Conclusion
Although the lack of toxicity supports
a safety finding for an exemption from
the requirement of tolerance for all
crops. EPA is establishing numerical
tolerances for residues resulting from
direct applications to certain
commodities because the petitioner
requested them for international trade
purposes. Therefore, tolerances are
established for residues of flutianil,
(2Z)-2-[2-fluoro-5(trifluoromethy)phenyl]sulfanyl-2-[3-(2methoxyphenyl)thiazolidin-2ylidene]acetonitrile, in or on apple at
0.15 ppm; apple, wet pomace at 0.30
ppm; cantaloupe at 0.07 ppm; cherry at
0.40 ppm; cucumber at 0.20 ppm; grape
at 0.70 ppm; squash at 0.05 ppm; and
strawberry at 0.50 ppm.
Additionally, an exemption from the
requirement of a tolerance is established
for indirect or inadvertent residues of
flutianil, (2Z)-2-[2-fluoro-5(trifluoromethy)phenyl]sulfanyl-2-[3-(2methoxyphenyl)thiazolidin-2ylidene]acetonitrile, in or on all food
commodities, except for those
commodities with tolerances
established.
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VI. Statutory and Executive Order
Reviews
This action establishes tolerances and
an exemption from the requirement of 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); Executive Order 13045,
entitled ‘‘Protection of Children from
Environmental Health Risks and Safety
Risks’’ (62 FR 19885, April 23, 1997); or
Executive Order 13771, entitled
‘‘Reducing Regulations and Controlling
Regulatory Costs’’ (82 FR 9339, February
3, 2017). 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 tolerances and exemption 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
PO 00000
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Fmt 4700
Sfmt 4700
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: March 8, 2018.
Richard P. Keigwin, Jr.,
Director, 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.
2. Add § 180.697 to subpart C to read
as follows:
■
§ 180.697
residues.
Flutianil; tolerances for
(a) General. Tolerances are
established for the combined residues of
the fungicide flutianil, including its
metabolites and degradates in or on food
commodities in the table below.
Compliance with the tolerance levels
specified below is to be determined by
measuring only flutianil, (2Z)-2-[2fluoro-5(trifluoromethyl)phenyl]sulfanyl-2-[3-(2methoxyphenyl)thiazolidin-2ylidene]acetonitrile in or on the
following commodities:
Commodity
Apple ...........................................
Apple, wet pomace .....................
Cantaloupe .................................
E:\FR\FM\21MRR1.SGM
21MRR1
Parts per
million
0.15
0.30
0.07
Federal Register / Vol. 83, No. 55 / Wednesday, March 21, 2018 / Rules and Regulations
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Cherry .........................................
0.40 Constitution Ave. NW, Washington, DC
Cucumber ...................................
0.20 20460–0001. The Public Reading Room
Grape ..........................................
0.70
is open from 8:30 a.m. to 4:30 p.m.,
Squash ........................................
0.05
Strawberry ..................................
0.50 Monday through Friday, excluding legal
holidays. The telephone number for the
(b) Section 18 emergency exemptions. Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
[Reserved]
Docket is (703) 305–5805. Please review
(c) Tolerances with regional
the visitor instructions and additional
registrations. [Reserved]
information about the docket available
(d) Indirect or inadvertent residues.
at https://www.epa.gov/dockets.
[Reserved]
FOR FURTHER INFORMATION CONTACT:
■ 3. Add § 180.1354 to subpart D to read
Michael Goodis, Registration Division
as follows:
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
§ 180.1354 Flutianil; exemption from the
Pennsylvania Ave. NW, Washington, DC
requirement of a tolerance.
20460–0001; main telephone number:
An exemption from the requirement
(703) 305–7090; email address:
of a tolerance is established for indirect
RDFRNotices@epa.gov.
and inadvertent residues of the
SUPPLEMENTARY INFORMATION:
fungicide flutianil, including its
metabolites and degradates, in or on all
I. General Information
food commodities not listed in
A. Does this action apply to me?
§ 180.697(a), when residues are present
therein as a result of uptake by crops
You may be potentially affected by
rotated into fields containing the crops
this action if you are an agricultural
in § 180.697(a) that were previously
producer, food manufacturer, or
treated with flutianil.
pesticide manufacturer. The following
list of North American Industrial
[FR Doc. 2018–05640 Filed 3–20–18; 8:45 am]
Classification System (NAICS) codes is
BILLING CODE 6560–50–P
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
ENVIRONMENTAL PROTECTION
applies to them. Potentially affected
AGENCY
entities may include:
40 CFR Part 180
• Crop production (NAICS code 111).
• Animal production (NAICS code
[EPA–HQ–OPP–2017–0211; FRL–9973–11]
112).
• Food manufacturing (NAICS code
S-Metolachlor; Pesticide Tolerances
311).
AGENCY: Environmental Protection
• Pesticide manufacturing (NAICS
Agency (EPA).
code 32532).
ACTION: Final rule.
B. How can I get electronic access to
Commodity
Parts per
million
This regulation establishes
tolerances for residues of S-metolachlor
in or on sugarcane, cane and sugarcane
molasses. Syngenta Crop Protection
requested these tolerances under the
Federal Food, Drug, and Cosmetic Act
(FFDCA).
SUMMARY:
This regulation is effective
March 21, 2018. Objections and requests
for hearings must be received on or
before May 21, 2018, and must be filed
in accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
sradovich on DSK3GMQ082PROD with RULES
DATES:
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2017–0211, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
ADDRESSES:
VerDate Sep<11>2014
16:29 Mar 20, 2018
Jkt 244001
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–2017–0211 in the subject line on
PO 00000
Frm 00023
Fmt 4700
Sfmt 4700
12269
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 May 21, 2018. 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–
2017–0211, 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 September
15, 2017 (82 FR 43352) (FRL–9965–43),
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 6F8519) by
Syngenta Crop Protection, LLC, P.O.
Box 18300, Greensboro, NC 27419. The
petition requested that 40 CFR part 180
be amended by establishing tolerances
for residues of the herbicide
S-metolachlor in or on sugarcane at 0.4
parts per million (ppm) and sugarcane
molasses at 1.5 ppm. That document
referenced a summary of the petition
prepared by Syngenta Crop Protection,
the registrant, which is available in the
docket, https://www.regulations.gov. A
comment was received on the notice of
filing. EPA’s response to this comment
is discussed in Unit IV.C.
Based upon review of the data
supporting the petition, EPA is
E:\FR\FM\21MRR1.SGM
21MRR1
Agencies
[Federal Register Volume 83, Number 55 (Wednesday, March 21, 2018)]
[Rules and Regulations]
[Pages 12265-12269]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-05640]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2015-0817; FRL-9974-32]
Flutianil; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes tolerances for residues of
flutianil in or on multiple commodities that are identified and
discussed later in this document and an exemption for indirect or
inadvertent residues of flutianil on other crops rotated into fields
previously treated with flutianil. OAT AGRIO Company, Ltd. requested
these tolerances under the Federal Food, Drug, and Cosmetic Act
(FFDCA).
DATES: This regulation is effective March 21, 2018. Objections and
requests for hearings must be received on or before May 21, 2018, 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-2015-0817, 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, Registration
Division (7505P), Office of Pesticide Programs, Environmental
Protection Agency, 1200
[[Page 12266]]
Pennsylvania Ave. NW, Washington, DC 20460-0001; main telephone number:
(703) 305-7090; 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 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/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-2015-0817 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
May 21, 2018. 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-2015-0817, 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 April 25, 2016 (81 FR 24044) (FRL-9944-
86), 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
5F8408) by OAT AGRIO Company, Ltd, 1-3-1 Kanda Ogawa-machi, Chiyoda-ku,
Tokyo 101-0052, Japan. The petition requested that 40 CFR part 180 be
amended by establishing tolerances for residues of the fungicide
flutianil, (2Z)-2-[2-fluoro-5-(trifluoromethyl)phenyl]sulfanyl-2-[3-(2-
methoxyphenyl)thiazolidin-2-ylidene]acetonitrile, in or on apple, fruit
at 0.2 parts per million (ppm); apple, juice at 0.03 ppm; apple, wet
pomace at 2 ppm; cantaloupe at 0.07 ppm; cherry, fruit at 0.4 ppm;
cucumber at 0.02 ppm; grape, fruit at 0.7 ppm; grape, juice at 0.2 ppm;
grape, raisins at 0.3 ppm; squash at 0.03 ppm; and strawberry, fruit at
0.3 ppm. That document referenced a summary of the petition prepared by
OAT AGRIO Company Ltd., the registrant, which is available in the
docket, https://www.regulations.gov. One comment was received on the
notice of filing. EPA's response to this comments is discussed in Unit
IV.C.
Following the publication of this notice, the petitioner revised
its petition by revising commodity terms to be consistent with the
terminology EPA uses for commodities, removing certain processed
commodities for which specific tolerances are not needed, amending
tolerance levels, and requesting an exemption to cover inadvertent
residues. EPA published a notice in the Federal Register of October 12,
2017 (82 FR 47422) (FRL-9967-09), pursuant to FFDCA section 408(d)(3),
21 U.S.C. 346a(d)(3), announcing OAT AGRIO Company's amended pesticide
petition (PP 5F8408). Superseding the original petition, the revised
petition requested that 40 CFR part 180 be amended by establishing
tolerances for residues of the fungicide flutianil in or on apple at
0.15 parts per million (ppm); apple, wet pomace at 0.30 ppm; cantaloupe
at 0.07 ppm; cherry at 0.40 ppm; cucumber at 0.20; ppm; grape at 0.70
ppm; squash at 0.05 ppm; and strawberry at 0.50 ppm. Additionally, OAT
AGRIO Company requested that an exemption from the requirement of a
tolerance be established in 40 CFR 180 for indirect or inadvertent
residues of fungicide, flutianil in or on all food commodities for
which tolerances are not separately established. Comments were received
on the notice of filing. EPA's response to these comments is discussed
in Unit IV.C.
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. . .
.''
Similarly, FFDCA section 408(c)(2) authorizes EPA to establish an
exemption from the requirement of a tolerance only if EPA determines
the exemption is ``safe'', which has the same definition for exemptions
as for tolerances and requires consideration of the same exposures and
factors as for tolerances. 21 U.S.C. 346a(c)(2)(B).
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
[[Page 12267]]
sufficient data to assess the hazards of and to make a determination on
aggregate exposure for flutianil including exposure resulting from the
tolerances established by this action. EPA's assessment of exposures
and risks associated with flutianil follows.
EPA has evaluated the available toxicity data and considered its
validity, completeness, and reliability as well as the relationship of
the results of the studies to human risk. EPA has also considered
available information concerning the variability of the sensitivities
of major identifiable subgroups of consumers, including infants and
children.
No single or repeated dose study performed by any route of exposure
produced an adverse effect following flutianil exposure below, at, or
above the limit dose (1,000 mg/kg/day). The only toxic effect of
flutianil exposure in the rat 28-day, 90-day, or 104-day oral toxicity
studies was associated with hyaline droplet formation in the renal
proximal tubular cells of males. No toxicity was observed in the female
rats dosed up to the limit dose for comparable time periods. An
immunohistochemical staining demonstrated that the hyaline droplets in
the proximal tubular cells were related to the presence of alpha-
2[micro]-globulin, which is not relevant for human toxicity. Based on
the link to alpha-2[micro]-globulin and the lack of any degenerative or
other associated effects, the hyaline droplet was not considered
biologically relevant to humans.
No toxicity was seen in the developmental, reproductive,
neurotoxic, or immunotoxic studies for flutianil. No dermal or systemic
toxicity was observed at the limit dose in the rat 28-day dermal
toxicity study. Nevertheless, in the rat 28-day inhalation toxicity
study, increased lung weights in females and histopathological findings
of minimal nasal mucous cell hypertrophy/hyperplasia and minimal lung
centriacinar inflammation in males and females were observed at the
highest dose tested. These observations were consistent with response
to aerosol exposure to an airway irritant. The nasal mucous cell
hypertrophy/hyperplasia is considered the physiological response of
these cells to irritant; however, the increased lung weights and
cellular inflammation reflect some degree of edema in air spaces, and
inflammation in the lung could affect airway responsiveness and
pulmonary function. Therefore, the increased lung weights in females
and lung lesions in both sexes were considered adverse effects.
Flutianil is classified as ``Not Likely to be Carcinogenic to Humans''
based on lack of evidence of carcinogenicity in rats and mice and no
evidence of mutagenicity. Flutianil produced no genotoxicity.
Specific information on the studies received and the nature of the
adverse effects caused by flutianil as well as the no-observed-adverse-
effect-level (NOAEL) and the lowest-observed-adverse-effect-level
(LOAEL) from the toxicity studies can be found at https://www.regulations.gov in document ``Flutianil. Draft Human Risk
Assessment to Support New Uses for a New Active Ingredient, Flutianil
on Apple, Cantaloupe, Cherry, Cucumber, Grape, Summer Squash, and
Strawberry'' dated November 1, 2017 in docket ID number EPA-HQ-OPP-
2015-0817.
Based on the analysis of the available flutianil toxicological
studies, there is no adverse toxicity from oral exposures seen in any
of the required submitted toxicology studies. No toxicity endpoint and
point of departure for regulating dietary exposure is established for
the human health risk assessment. There are no registered or proposed
residential uses at this time for flutianil; therefore, residential
handler and post-application exposure and risk were not assessed.
Flutianil is proposed for use on a variety of crops. Humans could
potentially be exposed to flutianil residues in food because flutianil
may be applied directly to growing crops. These applications can also
result in flutianil reaching surface and ground water, both of which
can serve as sources of drinking water. There are no proposed uses in
residential settings; therefore, there are no anticipated residential
exposures.
Based on the toxicological profile of flutianil, EPA has concluded
that the FFDCA requirements to retain an additional safety factor for
protection of infants and children and to consider cumulative effects
do not apply. Section 408(b)(2)(C) of the FFDCA (21 U.S.C. 346a)
requires an additional tenfold margin of safety in the case of
threshold risks, which are not present in this case. Section
408(b)(2)(D)(v) of the FFDCA requires consideration of information
concerning cumulative effects of substances that have a common
mechanism of toxicity, which flutianil does not have.
Based on the available data indicating a lack of adverse effects
from exposure to flutianil, EPA concludes that there is a reasonable
certainty that no harm will result to the general population, or to
infants and children from aggregate exposure to flutianil.
IV. Other Considerations
A. Analytical Enforcement Methodology
The gas chromatography-mass spectrometry detector (GC/MSD) is used
to measure and evaluate the chemical flutianil on apples, cantaloupe,
cherry, cucumber, squash, and strawberry. The high performance liquid
chromatography with tandem mass spectral detection (LCMS/MS) is used to
measure and evaluate the chemical flutianil and the metabolite OC-56635
in grapes.
Adequate enforcement methodology (gas chromatography) is available
to enforce the tolerance expression.
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.
The Codex has not established a MRL for flutianil.
C. Response to Comments
Several comments were received, although many simply expressed
concern about the use of pesticides on food generally. While EPA
recognizes that some individuals oppose the use of pesticides in or on
food, the FFDCA authorizes EPA to establish tolerances or exemptions
where it determines that doing so is safe. As required by the FFDCA,
EPA conducted a comprehensive assessment of flutianil, including its
potential for carcinogenicity. Based on its assessment of the available
data, the Agency believes that given the observed lack of toxicity of
this chemical, no risks of concern are expected. Therefore, EPA
concludes that the tolerances and exemption are safe and can be
supported. The commenters did not provide any information to indicate
otherwise.
[[Page 12268]]
Some comments (i.e., comments from the Center for Biological
Diversity (CBD)) were not relevant to this action because they raised
issues concerning compliance with the Endangered Species Act (ESA) and
the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), which
is not relevant to the determination needed to support tolerance
actions under the FFDCA.
Comments were received on the potential of flutianil to harm humans
based on the human health and environmental toxicity findings of the
European Food Safety Authority (EFSA). Although concerns were raised in
the EFSA report about the potential for carcinogenicity and
reproductive toxicity of flutianil, EPA has received additional data on
flutianil supporting the Agency's conclusions of a lack of
carcinogenicity or reproductive toxicity. Therefore, EPA concludes that
it has sufficient data to address the concerns raised by the EFSA
assessment and support its safety finding for flutianil. For further
information concerning these studies, see the ``Final Registration
Decision for the New Active Ingredient Flutianil: A Fungicide for Use
on Apples, Cantaloupes, Cherries, Cucumbers, Grapes, Squash, and
Strawberries'' [Docket ID Number EPA-HQ-OPP-2015-0817].
V. Conclusion
Although the lack of toxicity supports a safety finding for an
exemption from the requirement of tolerance for all crops. EPA is
establishing numerical tolerances for residues resulting from direct
applications to certain commodities because the petitioner requested
them for international trade purposes. Therefore, tolerances are
established for residues of flutianil, (2Z)-2-[2-fluoro-5-
(trifluoromethy)phenyl]sulfanyl-2-[3-(2-methoxyphenyl)thiazolidin-2-
ylidene]acetonitrile, in or on apple at 0.15 ppm; apple, wet pomace at
0.30 ppm; cantaloupe at 0.07 ppm; cherry at 0.40 ppm; cucumber at 0.20
ppm; grape at 0.70 ppm; squash at 0.05 ppm; and strawberry at 0.50 ppm.
Additionally, an exemption from the requirement of a tolerance is
established for indirect or inadvertent residues of flutianil, (2Z)-2-
[2-fluoro-5-(trifluoromethy)phenyl]sulfanyl-2-[3-(2-
methoxyphenyl)thiazolidin-2-ylidene]acetonitrile, in or on all food
commodities, except for those commodities with tolerances established.
VI. Statutory and Executive Order Reviews
This action establishes tolerances and an exemption from the
requirement of 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); Executive Order 13045, entitled ``Protection of
Children from Environmental Health Risks and Safety Risks'' (62 FR
19885, April 23, 1997); or Executive Order 13771, entitled ``Reducing
Regulations and Controlling Regulatory Costs'' (82 FR 9339, February 3,
2017). 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 tolerances and
exemption 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: March 8, 2018.
Richard P. Keigwin, Jr.,
Director, 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.
0
2. Add Sec. 180.697 to subpart C to read as follows:
Sec. [emsp14]180.697 Flutianil; tolerances for residues.
(a) General. Tolerances are established for the combined residues
of the fungicide flutianil, including its metabolites and degradates in
or on food commodities in the table below. Compliance with the
tolerance levels specified below is to be determined by measuring only
flutianil, (2Z)-2-[2-fluoro-5-(trifluoromethyl)phenyl]sulfanyl-2-[3-(2-
methoxyphenyl)thiazolidin-2-ylidene]acetonitrile in or on the following
commodities:
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
Apple....................................................... 0.15
Apple, wet pomace........................................... 0.30
Cantaloupe.................................................. 0.07
[[Page 12269]]
Cherry...................................................... 0.40
Cucumber.................................................... 0.20
Grape....................................................... 0.70
Squash...................................................... 0.05
Strawberry.................................................. 0.50
------------------------------------------------------------------------
(b) Section 18 emergency exemptions. [Reserved]
(c) Tolerances with regional registrations. [Reserved]
(d) Indirect or inadvertent residues. [Reserved]
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3. Add Sec. 180.1354 to subpart D to read as follows:
Sec. [emsp14]180.1354 Flutianil; exemption from the requirement of a
tolerance.
An exemption from the requirement of a tolerance is established for
indirect and inadvertent residues of the fungicide flutianil, including
its metabolites and degradates, in or on all food commodities not
listed in Sec. 180.697(a), when residues are present therein as a
result of uptake by crops rotated into fields containing the crops in
Sec. 180.697(a) that were previously treated with flutianil.
[FR Doc. 2018-05640 Filed 3-20-18; 8:45 am]
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