Florpyrauxifen-Benzyl; Pesticide Tolerances, 46685-46688 [2017-21614]
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178 (see also Unit I.C. of the
Final rule.
SUPPLEMENTARY INFORMATION).
[FR Doc. 2017–21504 Filed 10–5–17; 8:45 am]
asabaliauskas on DSKBBXCHB2PROD with RULES
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2016–0560; FRL–9963–66]
Florpyrauxifen-Benzyl; Pesticide
Tolerances
Environmental Protection
Agency (EPA).
AGENCY:
VerDate Sep<11>2014
16:21 Oct 05, 2017
This regulation establishes
tolerances for residues of
florpyrauxifen-benzyl in or on rice
grain, freshwater fish, shellfish
crustacean, and mollusc. Dow
AgroSciences LLC requested these
tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
SUMMARY:
BILLING CODE 6560–50–P
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This regulation is effective
October 6, 2017. Objections and
requests for hearings must be received
on or before December 5, 2017, and
must be filed in accordance with the
instructions provided in 40 CFR part
DATES:
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The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2016–0560, 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
ADDRESSES:
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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, 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).
• 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.
asabaliauskas on DSKBBXCHB2PROD with RULES
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–2016–0560 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 December 5, 2017. Addresses for
mail and hand delivery of objections
VerDate Sep<11>2014
16:21 Oct 05, 2017
Jkt 244001
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–
2016–0560, 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 December
20, 2016 (81 FR 92758) (FRL–9956–04),
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 5F8403) by Dow
AgroSciences LLC, 9330 Zionsville
Road, Indianapolis, IN 46268. The
petition requested that 40 CFR part 180
be amended by establishing tolerances
for residues of the herbicide
florpyrauxifen-benzyl (2Pyridinecarboxylic acid, 4-amino-3chloro-6-(4-chloro-2-fluoro-3methoxyphenyl)-5-fluoro-,
phenylmethyl ester) and florpyrauxifen
(metabolite; 2-Pyridinecarboxylic acid,
4-amino-3-chloro-6-(4-chloro-2-fluoro-3methoxyphenyl)-5-fluoro-), in or on the
raw agricultural commodities rice, grain
(dehulled) at 0.01 parts per million
(ppm); rice, grain at 0.2 ppm; fish,
freshwater at 2 ppm; shellfish,
crustacean at 0.5 ppm; and shellfish,
mollusk at 9 ppm. That document
referenced a summary of the petition
prepared by Dow AgroSciences LLC, the
registrant, which is available in the
docket, https://www.regulations.gov.
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There were no comments received in
response to the notice of filing.
Based upon review of the data
supporting the petition, EPA is
establishing tolerance levels that vary
from the petitioned-for levels for certain
crops and is correcting commodity
definitions, as needed, to be consistent
with current EPA policy. These changes
are explained further 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. . . .’’
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 florpyrauxifenbenzyl including exposure resulting
from the tolerances established by this
action. EPA’s assessment of exposures
and risks associated with
florpyrauxifen-benzyl 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.
Florpyrauxifen-benzyl is not
genotoxic and there were no treatmentrelated findings up to the limit dose
(1,000 milligrams/kilogram (mg/kg)/day)
or highest doses tested in the acute,
short-term, sub-chronic, or chronic oral
toxicity studies, two-generation
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Federal Register / Vol. 82, No. 193 / Friday, October 6, 2017 / Rules and Regulations
reproduction or developmental toxicity
studies or in the neurotoxicity study.
Chronic administration of
florpyrauxifen-benzyl did not show any
carcinogenicity potential and did not
cause any adverse effects in mice, rats
or dogs even up to the highest doses
tested.
Specific information on the studies
received and the nature of the adverse
effects caused by florpyrauxifen-benzyl
as well as the no-observed-adverseeffect-level (NOAEL) and the lowestobserved-adverse-effect-level (LOAEL)
from the toxicity studies can be found
at https://www.regulations.gov in
document ‘‘Florpyrauxifen-benzyl: New
Active Ingredient, First Food Use.
Human Health Risk Assessment for the
Establishment of Permanent Tolerances
on Rice, Fish, and Shellfish and
Registration for Uses on Rice and
Freshwater Aquatic Weed Control’’
dated December 1, 2016 in docket ID
number EPA–HQ–OPP–2016–0560.
Because no single or repeated dose
study performed by any route of
exposure produced an adverse effect
following florpyrauxifen-benzyl
exposure, toxicity endpoints and points
of departure were not selected for
florpyrauxifen-benzyl exposure
scenarios and a quantitative risk
assessment was not conducted. Instead,
a qualitative human health risk
assessment has been conducted to
support the proposed uses of
florpyrauxifen-benzyl.
Florpyrauxifen-benzyl is proposed for
use on rice and aquatic sites. Humans
could potentially be exposed to
florpyrauxifen-benzyl residues in food
(including fish and shellfish) because
florpyrauxifen-benzyl may be applied
directly to growing rice and aquatic
sites. These applications can also result
in florpyrauxifen-benzyl reaching
surface and ground water, both of which
can serve as sources of drinking water.
There are no proposed uses in
residential settings and there are no
anticipated residential exposures.
Section 408(b)(2)(C) of FFDCA
provides that EPA shall apply an
additional tenfold (10X) margin of safety
for infants and children in the case of
threshold effects to account for prenatal
and postnatal toxicity and the
completeness of the database on toxicity
and exposure, unless EPA determines
based on reliable data that a different
margin of safety will be safe for infants
and children. This additional margin of
safety is commonly referred to as the
FQPA Safety Factor (SF). In applying
this provision, EPA either retains the
default value of 10X, or uses a different
additional safety factor when reliable
data available to EPA support the choice
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16:21 Oct 05, 2017
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of a different factor. EPA considers the
toxicity database to be complete and
there are no residual uncertainties in the
florpyrauxifen-benzyl exposure
database. Because there are no threshold
effects in the florpyrauxifen-benzyl
database, the requirement to retain this
safety factor is inapplicable to the
current tolerance action.
Based on the lack of toxicity from
exposure to residues of florpyrauxifenbenzyl, 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 florpyrauxifen-benzyl.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate analytical enforcement
methodology which uses highperformance liquid chromatography
with tandem mass spectrometry (HPLC/
MS–MS) to quantitate residues of
florpyrauxifen-benzyl and
florpyrauxifen is available for
enforcement.
The method may be requested from:
Chief, Analytical Chemistry Branch,
Environmental Science Center, 701
Mapes Rd., Ft. Meade, MD 20755–5350;
telephone number: (410) 305–2905;
email address: residuemethods@
epa.gov.
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 florpyrauxifen-benzyl.
C. Revisions to Petitioned-For
Tolerances
Although a tolerance for rice, grain
(dehulled) was requested, EPA
determined that no such tolerance is
required. Rice, grain (dehulled) is
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46687
covered by the rice grain tolerance.
Based on the Organization of Economic
Cooperation and Development (OECD)
statistical calculation applied to the
field trial (U.S.) residue data, EPA
determined that the appropriate
tolerance level for rice, grain is 0.30
ppm. The OECD calculation procedures
are globally recognized for calculating
MRLs to facilitate the harmonization of
regulatory limits.
For fish-shellfish, mollusc the
tolerance level is established at 20 ppm,
rather than the requested 9 ppm, based
on the residue data. Also, to be
consistent with current EPA policy, the
commodity definitions were revised as
fish-freshwater finfish; fish-shellfish,
crustacean; and fish-shellfish, mollusc,
and the Agency added a significant
figure to the tolerances for rice, grain;
fish-freshwater finfish; and fishshellfish, crustacean.
V. Conclusion
Despite the lack of toxicity, the EPA
is establishing tolerances as requested
by the petitioner for international trade
purposes. Therefore, tolerances are
established for residues of
florpyrauxifen-benzyl, including its
metabolites and degradates, in or on
rice, grain at 0.30 ppm; fish-freshwater
finfish at 2.0 ppm; fish-shellfish,
crustacean at 0.50 ppm; and fishshellfish, mollusc at 20 ppm.
VI. Statutory and Executive Order
Reviews
This action establishes tolerances
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
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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
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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: September 8, 2017.
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 § 180.695 to subpart C to read
as follows:
■
§ 180.695 Florpyrauxifen-benzyl;
Pesticide Tolerances.
(a) General. Tolerances are
established for residues of
florpyrauxifen-benzyl, including its
metabolites and degradates, in or on the
commodities in the table below.
Compliance with the tolerance levels
specified below is to be determined by
measuring only the sum of
florpyrauxifen-benzyl (phenylmethyl 4-
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amino-3-chloro- 6-(4-chloro-2-fluoro-3methoxyphenyl)-5-fluoro-2pyridinecarboxylate) and its acid
metabolite (4-amino-3-chloro-6-(4chloro-2-fluoro-3-methoxyphenyl)-5fluoropyridine-2-carboxylic acid)
calculated as the stoichiometric
equivalent of florpyrauxifen-benzyl, in
or on the commodity.
Commodity
Parts per
million
Fish—freshwater finfish ........
Fish—shellfish, crustacean ...
Fish—shellfish, mollusc ........
Rice, grain ............................
2.0
0.50
20
0.30
(b) Section 18 emergency exemptions.
[Reserved]
(c) Tolerances with regional
registrations. [Reserved]
(d) Indirect or inadvertent residues.
[Reserved]
[FR Doc. 2017–21614 Filed 10–5–17; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Parts 1, 2, 15, 90, 95, and 97
[ET Docket No. 15–26; FCC 17–94]
Permitting Radar Services in the 76–81
GHz Band
Correction
In rule document 2017–18463
beginning on page 43865 in the issue of
Wednesday, September 20, 2017, make
the following correction:
§ 2.106
[Corrected]
In Part 2, in § 2.106, on page 43869,
the table should appear as follows:
■
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Agencies
[Federal Register Volume 82, Number 193 (Friday, October 6, 2017)]
[Rules and Regulations]
[Pages 46685-46688]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-21614]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2016-0560; FRL-9963-66]
Florpyrauxifen-Benzyl; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes tolerances for residues of
florpyrauxifen-benzyl in or on rice grain, freshwater fish, shellfish
crustacean, and mollusc. Dow AgroSciences LLC requested these
tolerances under the Federal Food, Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective October 6, 2017. Objections and
requests for hearings must be received on or before December 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-2016-0560, 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
[[Page 46686]]
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, 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).
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-2016-0560 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
December 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-2016-0560, 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 December 20, 2016 (81 FR 92758) (FRL-
9956-04), 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
5F8403) by Dow AgroSciences LLC, 9330 Zionsville Road, Indianapolis, IN
46268. The petition requested that 40 CFR part 180 be amended by
establishing tolerances for residues of the herbicide florpyrauxifen-
benzyl (2-Pyridinecarboxylic acid, 4-amino-3-chloro-6-(4-chloro-2-
fluoro-3-methoxyphenyl)-5-fluoro-, phenylmethyl ester) and
florpyrauxifen (metabolite; 2-Pyridinecarboxylic acid, 4-amino-3-
chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoro-), in or on the
raw agricultural commodities rice, grain (dehulled) at 0.01 parts per
million (ppm); rice, grain at 0.2 ppm; fish, freshwater at 2 ppm;
shellfish, crustacean at 0.5 ppm; and shellfish, mollusk at 9 ppm. That
document referenced a summary of the petition prepared by Dow
AgroSciences LLC, the registrant, which is available in the docket,
https://www.regulations.gov. There were no comments received in response
to the notice of filing.
Based upon review of the data supporting the petition, EPA is
establishing tolerance levels that vary from the petitioned-for levels
for certain crops and is correcting commodity definitions, as needed,
to be consistent with current EPA policy. These changes are explained
further 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. . .
.''
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 florpyrauxifen-benzyl including
exposure resulting from the tolerances established by this action.
EPA's assessment of exposures and risks associated with florpyrauxifen-
benzyl 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.
Florpyrauxifen-benzyl is not genotoxic and there were no treatment-
related findings up to the limit dose (1,000 milligrams/kilogram (mg/
kg)/day) or highest doses tested in the acute, short-term, sub-chronic,
or chronic oral toxicity studies, two-generation
[[Page 46687]]
reproduction or developmental toxicity studies or in the neurotoxicity
study. Chronic administration of florpyrauxifen-benzyl did not show any
carcinogenicity potential and did not cause any adverse effects in
mice, rats or dogs even up to the highest doses tested.
Specific information on the studies received and the nature of the
adverse effects caused by florpyrauxifen-benzyl 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 ``Florpyrauxifen-benzyl: New Active
Ingredient, First Food Use. Human Health Risk Assessment for the
Establishment of Permanent Tolerances on Rice, Fish, and Shellfish and
Registration for Uses on Rice and Freshwater Aquatic Weed Control''
dated December 1, 2016 in docket ID number EPA-HQ-OPP-2016-0560.
Because no single or repeated dose study performed by any route of
exposure produced an adverse effect following florpyrauxifen-benzyl
exposure, toxicity endpoints and points of departure were not selected
for florpyrauxifen-benzyl exposure scenarios and a quantitative risk
assessment was not conducted. Instead, a qualitative human health risk
assessment has been conducted to support the proposed uses of
florpyrauxifen-benzyl.
Florpyrauxifen-benzyl is proposed for use on rice and aquatic
sites. Humans could potentially be exposed to florpyrauxifen-benzyl
residues in food (including fish and shellfish) because florpyrauxifen-
benzyl may be applied directly to growing rice and aquatic sites. These
applications can also result in florpyrauxifen-benzyl reaching surface
and ground water, both of which can serve as sources of drinking water.
There are no proposed uses in residential settings and there are no
anticipated residential exposures.
Section 408(b)(2)(C) of FFDCA provides that EPA shall apply an
additional tenfold (10X) margin of safety for infants and children in
the case of threshold effects to account for prenatal and postnatal
toxicity and the completeness of the database on toxicity and exposure,
unless EPA determines based on reliable data that a different margin of
safety will be safe for infants and children. This additional margin of
safety is commonly referred to as the FQPA Safety Factor (SF). In
applying this provision, EPA either retains the default value of 10X,
or uses a different additional safety factor when reliable data
available to EPA support the choice of a different factor. EPA
considers the toxicity database to be complete and there are no
residual uncertainties in the florpyrauxifen-benzyl exposure database.
Because there are no threshold effects in the florpyrauxifen-benzyl
database, the requirement to retain this safety factor is inapplicable
to the current tolerance action.
Based on the lack of toxicity from exposure to residues of
florpyrauxifen-benzyl, 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 florpyrauxifen-benzyl.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate analytical enforcement methodology which uses high-
performance liquid chromatography with tandem mass spectrometry (HPLC/
MS-MS) to quantitate residues of florpyrauxifen-benzyl and
florpyrauxifen is available for enforcement.
The method may be requested from: Chief, Analytical Chemistry
Branch, Environmental Science Center, 701 Mapes Rd., Ft. Meade, MD
20755-5350; telephone number: (410) 305-2905; email address:
residuemethods@epa.gov.
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 florpyrauxifen-benzyl.
C. Revisions to Petitioned-For Tolerances
Although a tolerance for rice, grain (dehulled) was requested, EPA
determined that no such tolerance is required. Rice, grain (dehulled)
is covered by the rice grain tolerance. Based on the Organization of
Economic Cooperation and Development (OECD) statistical calculation
applied to the field trial (U.S.) residue data, EPA determined that the
appropriate tolerance level for rice, grain is 0.30 ppm. The OECD
calculation procedures are globally recognized for calculating MRLs to
facilitate the harmonization of regulatory limits.
For fish-shellfish, mollusc the tolerance level is established at
20 ppm, rather than the requested 9 ppm, based on the residue data.
Also, to be consistent with current EPA policy, the commodity
definitions were revised as fish-freshwater finfish; fish-shellfish,
crustacean; and fish-shellfish, mollusc, and the Agency added a
significant figure to the tolerances for rice, grain; fish-freshwater
finfish; and fish-shellfish, crustacean.
V. Conclusion
Despite the lack of toxicity, the EPA is establishing tolerances as
requested by the petitioner for international trade purposes.
Therefore, tolerances are established for residues of florpyrauxifen-
benzyl, including its metabolites and degradates, in or on rice, grain
at 0.30 ppm; fish-freshwater finfish at 2.0 ppm; fish-shellfish,
crustacean at 0.50 ppm; and fish-shellfish, mollusc at 20 ppm.
VI. Statutory and Executive Order Reviews
This action establishes tolerances 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
[[Page 46688]]
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: September 8, 2017.
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. 180.695 to subpart C to read as follows:
Sec. [emsp14]180.695 Florpyrauxifen-benzyl; Pesticide Tolerances.
(a) General. Tolerances are established for residues of
florpyrauxifen-benzyl, including its metabolites and degradates, in or
on the commodities in the table below. Compliance with the tolerance
levels specified below is to be determined by measuring only the sum of
florpyrauxifen-benzyl (phenylmethyl 4-amino-3-chloro- 6-(4-chloro-2-
fluoro-3-methoxyphenyl)-5-fluoro-2-pyridinecarboxylate) and its acid
metabolite (4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-
fluoropyridine-2-carboxylic acid) calculated as the stoichiometric
equivalent of florpyrauxifen-benzyl, in or on the commodity.
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
Fish--freshwater finfish................................ 2.0
Fish--shellfish, crustacean............................. 0.50
Fish--shellfish, mollusc................................ 20
Rice, grain............................................. 0.30
------------------------------------------------------------------------
(b) Section 18 emergency exemptions. [Reserved]
(c) Tolerances with regional registrations. [Reserved]
(d) Indirect or inadvertent residues. [Reserved]
[FR Doc. 2017-21614 Filed 10-5-17; 8:45 am]
BILLING CODE 6560-50-P