Fluensulfone; Pesticide Tolerances, 46156-46159 [2021-17682]
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46156
Federal Register / Vol. 86, No. 157 / Wednesday, August 18, 2021 / Rules and Regulations
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
of § 721.1725(b)(1) apply to paragraph
(a)(2)(ii) of this section.
§ 721.11442 Halogenated alkylbenzoic
acid, ethyl ester (generic) (P–19–108).
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(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as halogenated alkylbenzoic
acid, ethyl ester (PMN P–19–108) is
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Hazard communication.
Requirements as specified in § 721.72(a)
through (f), (g)(1), (g)(2)(i) through (iii),
(g)(3)(i) and (ii), and (g)(5). For purposes
of § 721.72(e), the concentration is set at
1.0%. For purposes of § 721.72(g)(1),
this substance may cause: Skin
irritation; respiratory complications;
central nervous system effects; internal
organ effects; reproductive effects;
developmental effects; eye irritation.
Alternative hazard and warning
statements that meet the criteria of the
Globally Harmonized System and OSHA
Hazard Communication Standard may
be used.
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(k) and (q). It is a
significant new use to manufacture or
process the substance without including
the engineering controls/processes
described in the premanufacture notice.
(iii) Release to water. Requirements as
specified in § 721.90(a)(4), (b)(4), and
(c)(4) where N=14.
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph (b).
(1) Recordkeeping. Recordkeeping
requirements as specified in
§ 721.125(a) through (c), (f) through (i),
and (k) are applicable to manufacturers
and processors of this substance.
(2) Limitation or revocation of certain
notification requirements. The
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
of § 721.1725(b)(1) apply to paragraph
(a)(2)(ii) of this section.
§ 721.11443 Halogenated benzoic acid,
ethyl ester (generic) (P–19–110).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as halogenated benzoic acid,
ethyl ester (PMN P–19–110) is subject to
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reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Hazard communication.
Requirements as specified in § 721.72(a)
through (f), (g)(1), (g)(2)(i) through (iii),
(g)(3)(i) and (ii), and (g)(5). For purposes
of § 721.72(e), the concentration is set at
1.0%. For purposes of § 721.72(g)(1),
this substance may cause: Skin
irritation; respiratory complications;
central nervous system effects; internal
organ effects; reproductive effects;
developmental effects; eye irritation.
Alternative hazard and warning
statements that meet the criteria of the
Globally Harmonized System and OSHA
Hazard Communication Standard may
be used.
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(k) and (q). It is a
significant new use to manufacture or
process the substance without including
the engineering controls/processes
described in the premanufacture notice.
(iii) Release to water. Requirements as
specified in § 721.90(a)(4), (b)(4), and
(c)(4) where N=14.
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph (b).
(1) Recordkeeping. Recordkeeping
requirements as specified in
§ 721.125(a) through (c), (f) through (i),
and (k) are applicable to manufacturers
and processors of this substance.
(2) Limitation or revocation of certain
notification requirements. The
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
of § 721.1725(b)(1) apply to paragraph
(a)(2)(ii) of this section.
[FR Doc. 2021–17392 Filed 8–17–21; 8:45 am]
BILLING CODE 6560–50–P
Federal Food, Drug, and Cosmetic Act
(FFDCA).
This regulation is effective
August 18, 2021. Objections and
requests for hearings must be received
on or before October 18, 2021, 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–2020–0118, 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.
Due to the public health concerns
related to COVID–19, the EPA Docket
Center (EPA/DC) and Reading Room is
closed to visitors with limited
exceptions. The staff continues to
provide remote customer service via
email, phone, and webform. For the
latest status information on EPA/DC
services and docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Marietta Echeverria, 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:
DATES:
I. General Information
A. Does this action apply to me?
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2020–0118; FRL–8653–01–
OCSPP]
Fluensulfone; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
tolerance for residues of fluensulfone in
or on soybean, seed. Makhteshim Agan
of North America (d/b/a ADAMA)
requested these tolerances under the
SUMMARY:
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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).
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Federal Register / Vol. 86, No. 157 / Wednesday, August 18, 2021 / Rules and Regulations
B. How can I get electronic access to
other related information?
II. Summary of Petitioned-For
Tolerance
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Publishing Office’s eCFR site at https://www.ecfr.gov/cgi-bin/
text-idx?&c=ecfr&tpl=/ecfrbrowse/
Title40/40tab_02.tpl.
In the Federal Register of April 15,
2020 (85 FR 20910) (FRL–10006–54),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of
pesticide petition (PP 9F8799) by
Makhteshim Agan of North America (d/
b/a ADAMA), 3120 Highwoods Blvd.,
Suite 100, Raleigh, NC 27604. The
petition requested that 40 CFR 180.680
be amended by establishing tolerances
for residues of the nematicide
fluensulfone, in or on soybean, seed at
0.1 parts per million (ppm); soybean,
forage at 7.0 ppm; and soybean, hay at
20 ppm. That document referenced a
summary of the petition prepared by
Makhteshim Agan of North America, the
petitioner, which is available in the
docket, https://www.regulations.gov.
Two comments were received on the
notice of filing. EPA’s response to these
comments is discussed in Unit IV.C.
Based upon review of the data
supporting the petition, EPA is
establishing a tolerance that varies from
what is requested. The reason for these
changes is explained in Unit IV.D.
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C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a(g), 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–2020–0118 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
October 18, 2021. 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–
2020–0118, 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.
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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
therein, 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 fluensulfone,
including exposure resulting from the
tolerance established by this action.
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EPA’s assessment of exposures and risks
associated with fluensulfone follows.
In an effort to streamline Federal
Register publications, EPA is not
reprinting here summaries of its
analyses that have previously appeared
in the Federal Register in previous
tolerance rulemakings for the same
pesticide. To that end, this rulemaking
refers the reader to several sections from
the April 13, 2018 tolerance rulemaking
for residues of fluensulfone that remain
unchanged for an understanding of the
Agency’s rationale in support of this
rulemaking. See 83 FR 15971 (FRL–
9975–76). Those sections are: Units III.A
(Toxicological Profile); III.B.
(Toxicological Points of Departure/
Levels of Concern); and III.C. (Exposure
Assessment), except as explained in the
next paragraphs; III.D. (Safety Factor for
Infants and Children).
Exposure assessment updates. EPA’s
exposure assessments have been
updated to include the additional
exposure from use of fluensulfone on
soybeans. EPA’s aggregate exposure
assessment incorporated this additional
dietary exposure, as well as exposure
from drinking water and from
residential sources. The new use does
not result in an increase in the
estimated residue levels in drinking
water or in exposure from residential
sources relative to those used in the last
assessment.
Further information about EPA’s risk
assessment and determination of safety
supporting the new fluensulfone
tolerance can be found at https://
www.regulations.gov in the document
titled ‘‘Fluensulfone. Human Health
Risk Assessment for a New Use on
Soybean.’’ in docket ID EPA–HQ–OPP–
2020–0118.
Assessment of aggregate risks. EPA
determines whether acute and chronic
dietary pesticide exposures are safe by
comparing aggregate exposure estimates
to the acute population adjusted dose
(aPAD) and chronic population adjusted
dose (cPAD). Short-, intermediate-, and
chronic-term risks are evaluated by
comparing the estimated aggregate food,
water, and residential exposure to the
appropriate points of departure (PODs)
to ensure that an adequate margin of
exposure (MOE) exists. For linear cancer
risks, EPA calculates the lifetime
probability of acquiring cancer given the
estimated aggregate exposure.
Acute dietary risks are below the
Agency’s level of concern: The acute
dietary risk estimate is 21% of the aPAD
for infants (<1 year old), the group with
the highest exposure. Chronic dietary
risks are below the Agency’s level of
concern: 4.8% of the cPAD for infants
(<1 year old), the group with the highest
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Federal Register / Vol. 86, No. 157 / Wednesday, August 18, 2021 / Rules and Regulations
exposure. EPA has concluded the
combined short-term food, water, and
residential exposures result in aggregate
margins of exposure above the level of
concern of 100 for all scenarios assessed
and are not of concern. EPA has
determined that quantification of cancer
risk using a non-linear approach (i.e.,
reference dose) will adequately account
for all chronic toxicity, including
carcinogenicity, that could result from
exposure to fluensulfone; the chronic
aggregate assessment did not result in
risk estimates of concern.
Determination of safety. Therefore,
based on the risk assessments and
information described above, EPA
concludes there is a reasonable certainty
that no harm will result to the general
population, or to infants and children,
from aggregate exposure to fluensulfone
residues. More detailed information on
this action to establish a tolerance on
soybean can be found in the document
entitled, ‘‘Fluensulfone. Human Health
Risk Assessment for a new use on
Soybean’’ by going to the docket
established by this action, which is
described under ADDRESSES.
IV. Other Considerations
A. Analytical Enforcement Methodology
There are adequate residue analytical
methods for enforcing tolerances for
fluensulfone residues of concern in/on
the registered plant and livestock
commodities. These methods include
two high-performance liquid
chromatography methods with tandem
mass-spectroscopy detection (HPLC/
MS/MS) for determining residues in/on
plant and livestock matrices.
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.
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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).
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 fluensulfone on soybean.
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C. Response to Comments
EPA received two comments from
anonymous sources. One comment cited
concern regarding fluoride; this
comment is not relevant to the Agency’s
evaluation of a tolerance for the
proposed new use of fluensulfone on
soybean. The other comment expresses
concern about pesticides in general, and
requests that the Agency deny use of
fluensulfone without specifically
mentioning the new use on soybean.
While the agency recognizes that some
people do not like pesticides, the
Agency has evaluated the aggregate risk
of fluensulfone and has determined that
there is a reasonable certainty that no
harm will result to the general
population, or to infants and children,
from aggregate exposure to fluensulfone
residues.
D. Revisions to Petitioned-For
Tolerances
The agency has determined that
tolerances are not needed for soybean,
forage and soybean, hay, as the label
contains a feeding restriction for those
commodities, and the commodities will
not be in the channels of trade. Further,
the agency has recommended amending
the proposed tolerance for soybean, seed
from 0.1 ppm to 0.07 ppm based upon
the OECD MRL/Tolerance Calculation
Procedures.
V. Conclusion
Therefore, a tolerance is established
for residues of fluensulfone on soybean,
seed at 0.07 ppm.
VI. Statutory and Executive Order
Reviews
This action establishes a tolerance
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997). This action does not
contain any information collections
subject to OMB approval under the
Paperwork Reduction Act (PRA) (44
U.S.C. 3501 et seq.), nor does it require
any special considerations under
Executive Order 12898, entitled
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‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerance in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or Tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
has determined that this action will not
have a substantial direct effect on States
or Tribal Governments, on the
relationship between the National
Government and the States or Tribal
Governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, the Agency has determined
that Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999) and Executive Order 13175,
entitled ‘‘Consultation and Coordination
with Indian Tribal Governments’’ (65 FR
67249, November 9, 2000) do not apply
to this action. In addition, this action
does not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act (UMRA) (2 U.S.C.
1501 et seq.).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
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Federal Register / Vol. 86, No. 157 / Wednesday, August 18, 2021 / Rules and Regulations
Dated: August 6, 2021.
Marietta Echeverria,
Acting Director, Registration Division, Office
of Pesticide Programs.
PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
CHEMICAL RESIDUES IN FOOD
Therefore, for the reasons stated in the
preamble, EPA is amending 40 CFR
chapter I as follows:
■
2. In § 180.680, amend the table 1 to
§ 180.680 by adding in alphabetical
order in paragraph (a) the entry
‘‘Soybean, seed’’ to read as follows:
■
1. The authority citation for part 180
continues to read as follows:
§ 180.680 Fluensulfone; tolerances for
residues.
Authority: 21 U.S.C. 321(q), 346a and 371.
(a) * * *
TABLE 1 TO § 180.680
Parts per
million
Commodity
*
*
*
*
*
*
Soybean, seed .......................................................................................................................................................................................
*
*
*
*
*
*
*
*
*
*
*
[FR Doc. 2021–17682 Filed 8–17–21; 8:45 am]
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0.07
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Agencies
[Federal Register Volume 86, Number 157 (Wednesday, August 18, 2021)]
[Rules and Regulations]
[Pages 46156-46159]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-17682]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2020-0118; FRL-8653-01-OCSPP]
Fluensulfone; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes tolerance for residues of
fluensulfone in or on soybean, seed. Makhteshim Agan of North America
(d/b/a ADAMA) requested these tolerances under the Federal Food, Drug,
and Cosmetic Act (FFDCA).
DATES: This regulation is effective August 18, 2021. Objections and
requests for hearings must be received on or before October 18, 2021,
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-2020-0118, 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.
Due to the public health concerns related to COVID-19, the EPA
Docket Center (EPA/DC) and Reading Room is closed to visitors with
limited exceptions. The staff continues to provide remote customer
service via email, phone, and webform. For the latest status
information on EPA/DC services and docket access, visit https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Marietta Echeverria, 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:
[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).
[[Page 46157]]
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
Publishing 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(g), 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-2020-0118 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
October 18, 2021. 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-2020-0118, 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 15, 2020 (85 FR 20910) (FRL-10006-
54), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of pesticide petition (PP
9F8799) by Makhteshim Agan of North America (d/b/a ADAMA), 3120
Highwoods Blvd., Suite 100, Raleigh, NC 27604. The petition requested
that 40 CFR 180.680 be amended by establishing tolerances for residues
of the nematicide fluensulfone, in or on soybean, seed at 0.1 parts per
million (ppm); soybean, forage at 7.0 ppm; and soybean, hay at 20 ppm.
That document referenced a summary of the petition prepared by
Makhteshim Agan of North America, the petitioner, which is available in
the docket, https://www.regulations.gov. Two comments were received on
the notice of filing. EPA's response to these comments is discussed in
Unit IV.C.
Based upon review of the data supporting the petition, EPA is
establishing a tolerance that varies from what is requested. The reason
for these changes is explained in Unit IV.D.
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 therein, 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 fluensulfone, including exposure resulting from
the tolerance established by this action. EPA's assessment of exposures
and risks associated with fluensulfone follows.
In an effort to streamline Federal Register publications, EPA is
not reprinting here summaries of its analyses that have previously
appeared in the Federal Register in previous tolerance rulemakings for
the same pesticide. To that end, this rulemaking refers the reader to
several sections from the April 13, 2018 tolerance rulemaking for
residues of fluensulfone that remain unchanged for an understanding of
the Agency's rationale in support of this rulemaking. See 83 FR 15971
(FRL-9975-76). Those sections are: Units III.A (Toxicological Profile);
III.B. (Toxicological Points of Departure/Levels of Concern); and
III.C. (Exposure Assessment), except as explained in the next
paragraphs; III.D. (Safety Factor for Infants and Children).
Exposure assessment updates. EPA's exposure assessments have been
updated to include the additional exposure from use of fluensulfone on
soybeans. EPA's aggregate exposure assessment incorporated this
additional dietary exposure, as well as exposure from drinking water
and from residential sources. The new use does not result in an
increase in the estimated residue levels in drinking water or in
exposure from residential sources relative to those used in the last
assessment.
Further information about EPA's risk assessment and determination
of safety supporting the new fluensulfone tolerance can be found at
https://www.regulations.gov in the document titled ``Fluensulfone. Human
Health Risk Assessment for a New Use on Soybean.'' in docket ID EPA-HQ-
OPP-2020-0118.
Assessment of aggregate risks. EPA determines whether acute and
chronic dietary pesticide exposures are safe by comparing aggregate
exposure estimates to the acute population adjusted dose (aPAD) and
chronic population adjusted dose (cPAD). Short-, intermediate-, and
chronic-term risks are evaluated by comparing the estimated aggregate
food, water, and residential exposure to the appropriate points of
departure (PODs) to ensure that an adequate margin of exposure (MOE)
exists. For linear cancer risks, EPA calculates the lifetime
probability of acquiring cancer given the estimated aggregate exposure.
Acute dietary risks are below the Agency's level of concern: The
acute dietary risk estimate is 21% of the aPAD for infants (<1 year
old), the group with the highest exposure. Chronic dietary risks are
below the Agency's level of concern: 4.8% of the cPAD for infants (<1
year old), the group with the highest
[[Page 46158]]
exposure. EPA has concluded the combined short-term food, water, and
residential exposures result in aggregate margins of exposure above the
level of concern of 100 for all scenarios assessed and are not of
concern. EPA has determined that quantification of cancer risk using a
non-linear approach (i.e., reference dose) will adequately account for
all chronic toxicity, including carcinogenicity, that could result from
exposure to fluensulfone; the chronic aggregate assessment did not
result in risk estimates of concern.
Determination of safety. Therefore, based on the risk assessments
and information described above, EPA concludes there is a reasonable
certainty that no harm will result to the general population, or to
infants and children, from aggregate exposure to fluensulfone residues.
More detailed information on this action to establish a tolerance on
soybean can be found in the document entitled, ``Fluensulfone. Human
Health Risk Assessment for a new use on Soybean'' by going to the
docket established by this action, which is described under ADDRESSES.
IV. Other Considerations
A. Analytical Enforcement Methodology
There are adequate residue analytical methods for enforcing
tolerances for fluensulfone residues of concern in/on the registered
plant and livestock commodities. These methods include two high-
performance liquid chromatography methods with tandem mass-spectroscopy
detection (HPLC/MS/MS) for determining residues in/on plant and
livestock matrices.
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:
[email protected].
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). 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 fluensulfone on soybean.
C. Response to Comments
EPA received two comments from anonymous sources. One comment cited
concern regarding fluoride; this comment is not relevant to the
Agency's evaluation of a tolerance for the proposed new use of
fluensulfone on soybean. The other comment expresses concern about
pesticides in general, and requests that the Agency deny use of
fluensulfone without specifically mentioning the new use on soybean.
While the agency recognizes that some people do not like pesticides,
the Agency has evaluated the aggregate risk of fluensulfone and has
determined that there is a reasonable certainty that no harm will
result to the general population, or to infants and children, from
aggregate exposure to fluensulfone residues.
D. Revisions to Petitioned-For Tolerances
The agency has determined that tolerances are not needed for
soybean, forage and soybean, hay, as the label contains a feeding
restriction for those commodities, and the commodities will not be in
the channels of trade. Further, the agency has recommended amending the
proposed tolerance for soybean, seed from 0.1 ppm to 0.07 ppm based
upon the OECD MRL/Tolerance Calculation Procedures.
V. Conclusion
Therefore, a tolerance is established for residues of fluensulfone
on soybean, seed at 0.07 ppm.
VI. Statutory and Executive Order Reviews
This action establishes a tolerance under FFDCA section 408(d) in
response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001) or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997). This action does not contain any
information collections subject to OMB approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et seq.), nor does it require any
special considerations under Executive Order 12898, entitled ``Federal
Actions to Address Environmental Justice in Minority Populations and
Low-Income Populations'' (59 FR 7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerance in this
final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or Tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
Tribal Governments, on the relationship between the National Government
and the States or Tribal Governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian tribes. Thus, the Agency has
determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999) and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November 9, 2000) do not apply to this action. In addition, this
action does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
(UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
[[Page 46159]]
Dated: August 6, 2021.
Marietta Echeverria,
Acting Director, Registration Division, Office of Pesticide Programs.
Therefore, for the reasons stated in the preamble, EPA is amending
40 CFR chapter I as follows:
PART 180--TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES
IN FOOD
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. In Sec. 180.680, amend the table 1 to Sec. 180.680 by adding in
alphabetical order in paragraph (a) the entry ``Soybean, seed'' to read
as follows:
Sec. 180.680 Fluensulfone; tolerances for residues.
(a) * * *
Table 1 to Sec. 180.680
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * * * *
Soybean, seed............................................. 0.07
* * * * * * *
------------------------------------------------------------------------
* * * * *
[FR Doc. 2021-17682 Filed 8-17-21; 8:45 am]
BILLING CODE 6560-50-P