[Federal Register Volume 88, Number 175 (Tuesday, September 12, 2023)]
[Rules and Regulations]
[Pages 62464-62471]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-19607]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2020-0065; FRL-8786-01-OCSPP]
Fluazaindolizine; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes tolerances for residues of
fluazaindolizine in or on multiple commodities that are identified and
discussed later in this document. E.I. du Pont de Nemours & Company
(``DuPont'', now Corteva) requested these tolerances under the Federal
Food, Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective September 12, 2023. Objections and
requests for hearings must be received on or before November 13, 2023,
and must be filed in accordance with the instructions provided in 40
CFR part
[[Page 62465]]
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-2020-0065, is available online at
http://www.regulations.gov or in-person 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 and the OPP Docket is (202) 566-
1744. For the latest status information on EPA/DC services and docket
access, visit https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Charles Smith, Director, Registration
Division (7505T), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-
0001; main telephone number: (202) 566-1030; 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 Office of the
Federal Register's e-CFR site at https://www.ecfr.gov/current/title40.
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-2020-0065 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
November 13, 2023. 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-2020-0065, by one of
the following methods:
Federal eRulemaking Portal: http://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 http://www.epa.gov/dockets.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at http://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 a pesticide petition (PP
9F8795) by E.I. du Pont de Nemours & Company (``DuPont''), Chestnut Run
Plaza, 974 Centre Road, Wilmington, DE 19805. The petition requested to
establish tolerances in the 40 CFR part 180 for residues of the
nematicide, fluazaindolizine, by measuring the sum of post-hydrolysis
residues IN-A5760, IN-F4106, IN-QEK31, IN-QZY47, IN-TMQ01, IN-UJV12,
and IN-UNS90 (expressed in parent equivalents) in or on Carrots at 15
parts per million (ppm); Cucurbit Vegetables (Crop Group 9) at 3 ppm;
Fruiting Vegetables (Crop Group 8-10) at 3 ppm; Sun dried tomatoes at
30 ppm; Tomato paste at 15 ppm; Tomato puree at 6 ppm; Tomato wet
pomace at 6 ppm; Tuberous and Corm Vegetables (Crop Subgroup 1C) at 9
ppm; Dried potato at 30 ppm; Potato process waste at 40 ppm; and
establishing tolerances for residues of fluazaindolizine plus its
metabolites IN-QEK and IN-F4106 (expressed in parent equivalents), in
the animal commodities: Cattle, whole milk at 0.5 ppm; Cattle, fat at
0.09 ppm; Cattle, muscle at 0.02 ppm; Cattle, liver at 0.2 ppm; Cattle,
kidney at 0.5 ppm; Goat, whole milk at 0.5 ppm; Goat, fat at 0.09 ppm;
Goat, muscle at 0.02 ppm; Goat, liver at 0.2 ppm; Goat, kidney at 0.5
ppm; Hog, whole milk at 0.5 ppm; Hog, fat at 0.09 ppm; Hog, muscle at
0.02 ppm; Hog, liver at 0.2 ppm; Hog, kidney at 0.5 ppm; Horse, whole
milk at 0.5 ppm; Horse, fat at 0.09 ppm; Horse, muscle at 0.02 ppm;
Horse, liver at 0.2 ppm; Horse, kidney at 0.5 ppm; Sheep, whole milk at
0.5 ppm; Sheep, fat at 0.09 ppm; Sheep, muscle at 0.02 ppm; Sheep,
liver at 0.2 ppm; Sheep, kidney at 0.5 ppm. In addition, DuPont
proposed pursuant to section 408(d) of the Federal Food, Drug and
Cosmetic Act, 21 U.S.C. 346a(d), to amend 40 CFR part 180 to establish
indirect or inadvertent tolerances for residues of fluazaindolizine, by
measuring the sum of post-hydrolysis residues IN-A5760, IN-F4106, IN-
QEK31, IN-QZY47, IN-TMQ01, IN-UJV12, and IN-UNS90 (expressed in parent
equivalents) in or on the following commodities: Brassica Head and Stem
Vegetables (Crop Group 5-16) at 0.5 ppm; Bulb Vegetables (Crop Group 3-
07) at 3 ppm; Cereal Grains (Crop Group 15) at 3 ppm; Corn milled by-
products at 6 ppm; Foliage of Legume Vegetables (Crop Group 7), Vines
at 8 ppm; Foliage of Legume Vegetables (Crop Group 7), Forage and Straw
at 5 ppm; Foliage of Legume Vegetables (Crop Group 7), Hay at 40 ppm;
Forage, Fodder and Straw of Cereal Grains (Crop Group 16), Fodder at 4
ppm; Forage, Fodder and Straw of Cereal Grains (Crop Group 16), Forage
at 8 ppm; Forage, Fodder and Straw of Cereal Grains (Crop Group 16),
Hay at 15 ppm; Forage, Fodder and Straw of Cereal Grains (Crop Group
16), Straw at 10 ppm; Fruiting Vegetables (Crop Group 8-10) at 1 ppm;
Grain, Aspirated Fractions at 0.5 ppm; Grass, Forage, Fodder and Hay
(Crop Group 17), Forage at 8 ppm; Grass, Forage, Fodder and Hay (Crop
Group 17), Hay at 15
[[Page 62466]]
ppm; Leafy Vegetables (Crop Group 4-16) at 9 ppm; Leaves of Root and
Tuber (Crop Group 2) at 15 ppm; Legume Vegetables (Crop Group 6),
Mature Seed at 9 ppm; Legume Vegetables (Crop Group 6), Immature Seed
and Pod at 3 ppm; Low Growing Berry (Crop Subgroup 13-07G) at 0.6 ppm;
Nongrass Animal Feeds (Forage, Fodder, Straw and Hay) (Crop Group 18),
Fodder at 5 ppm; Nongrass Animal Feeds (Forage, Fodder, Straw and Hay)
(Crop Group 18), Forage at 8 ppm; Nongrass Animal Feeds (Forage,
Fodder, Straw and Hay) (Crop Group 18), Hay at 15 ppm; Nongrass Animal
Feeds (Forage, Fodder, Straw and Hay) (Crop Group 18), Straw at 10 ppm;
Oilseed (Crop Group 20) at 9 ppm; Oilseed Crop Group 20), Forage and
Straw at 5 ppm; Root Vegetables (Crop Subgroup 1A) at 7 ppm; Root
Vegetables Except Sugar Beet (Crop Subgroup 1B) at 7 ppm; Soybean Hulls
at 20 ppm; Soybean Meal at 20 ppm; Stalk, Stem and Leaf Petiole
Vegetables (Crop Group 22) at 3 ppm; Strawberry, Dehydrated at 3 ppm;
and Wheat Milled By-Products at 6 ppm. That document referenced a
summary of the petition prepared by DuPont (now Corteva), the
registrant, which is available in the docket, http://www.regulations.gov. A comment was received on the notice of filing.
EPA's response to this comment is discussed in Unit IV.C.
In the Federal Register of June 28, 2021 (86 FR 33922) (FRL-10025-
08), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), amending the previous NOF dated April 15, 2020 by
announcing commodities that were not included in the previous NOF. E.I.
du Pont de Nemours & Company (``DuPont''), Chestnut Run Plaza, 974
Centre Road, Wilmington, DE 19805, requests to establish a tolerance in
40 CFR part 180 for residues of the nematicide, fluazaindolizine in or
on Poultry, fat at 0.01 ppm; Poultry, meat at 0.01 ppm; Poultry, meat
byproducts at 0.01 ppm; and Eggs at 0.01 ppm. In addition, DuPont is
proposing pursuant to section 408(d) of the Federal Food, Drug and
Cosmetic Act, 21 U.S.C. 346a(d), to amend 40 CFR part 180 to establish
indirect or inadvertent tolerances for residues of fluazaindolizine,
including its metabolites and their conjugates, expressed as the
stoichiometric equivalent of fluazaindolizine, in or on the following
commodity: Grass, forage, fodder and hay, group 17, straw at 0.15 ppm.
Based upon review of the data supporting the petition, EPA is
establishing tolerances at different levels than petitioned-for and has
determined that tolerances for certain petitioned-for commodities are
not necessary. The Agency has also modified all of the commodity
definitions used and updated certain crop groups. The reasons for these
changes are 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 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 fluazaindolizine including
exposure resulting from the tolerances established by this action.
EPA's assessment of exposures and risks associated with
fluazaindolizine follows.
A. Toxicological Profile
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.
The main target organs of fluazaindolizine are the urinary tract
(rat and mouse), liver and/or gallbladder (mouse and dog), and
hematopoietic system (dog). In the mouse carcinogenicity study, the
incidence and severity of amyloidosis in specific tissues was increased
in both sexes. There was no evidence of increased in utero
susceptibility in the rat or rabbit developmental studies; however,
increased quantitative susceptibility was observed in the rat
reproductive toxicity study, based on urinary tract histopathological
lesions in F2 generation weanlings at a lower dose than
doses resulting in toxicity in parental animals. Fluazaindolizine is
classified as ``Not likely to be carcinogenic to humans'' based on lack
of evidence of treatment-related increases in tumors in adequately
conducted carcinogenicity studies in rats and mice.
Specific information on the studies received and the nature of the
adverse effects caused by fluazaindolizine 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 http://www.regulations.gov in the document titled ``Fluazaindolizine: Human
Health Risk Assessment for the New Active Ingredient'' (hereinafter
``Fluazaindolizine Human Health Risk Assessment'') on pages 54-82 in
docket ID number EPA-HQ-OPP-2020-0065.
B. Toxicological Points of Departure/Levels of Concern
Once a pesticide's toxicological profile is determined, EPA
identifies toxicological points of departure (POD) and levels of
concern to use in evaluating the risk posed by human exposure to the
pesticide. For hazards that have a threshold below which there is no
appreciable risk, the toxicological POD is used as the basis for
derivation of reference values for risk assessment. PODs are developed
based on a careful analysis of the doses in each toxicological study to
determine the dose at which no adverse effects are observed (the NOAEL)
and the lowest dose at which adverse effects of concern are identified
(the LOAEL). Uncertainty/safety factors are used in conjunction with
the POD to calculate a safe exposure level--generally referred to as a
population-adjusted dose (PAD) or a reference dose (RfD)--and a safe
margin of exposure (MOE). For non-threshold risks, the Agency assumes
that any amount of exposure will lead to some degree of risk. Thus, the
Agency estimates risk in terms of the probability of an occurrence of
the adverse effect expected in a lifetime. For more information on the
general principles EPA uses in risk characterization and a complete
description of the risk assessment process, see http://www.epa.gov/pesticide-science-and-assessing-pesticide-risks.
A summary of the toxicological endpoints for fluazaindolizine used
for
[[Page 62467]]
human risk assessment can be found in the Fluazaindolizine Human Health
Risk Assessment.
C. Exposure Assessment
1. Dietary exposure from food and feed uses. In evaluating dietary
exposure to fluazaindolizine, EPA considered exposure under the
petitioned-for tolerances. EPA assessed dietary exposures from
fluazaindolizine in food as follows:
i. Acute exposure. Quantitative acute dietary exposure and risk
assessments are performed for a food-use pesticide, if a toxicological
study has indicated the possibility of an effect of concern occurring
as a result of a 1-day or single exposure.
No such effects were identified in the toxicological studies for
fluazaindolizine; therefore, a quantitative acute dietary exposure
assessment is unnecessary.
ii. Chronic exposure. In conducting the chronic dietary exposure
assessment, EPA used the 2003-2008 food consumption data from the U.S.
Department of Agriculture's National Health and Nutrition Examination
Survey, What We Eat in America (NHANES/WWEIA). As to residue levels in
food, EPA used field-trial based anticipated residue calculations for
all crops and assumed 100 percent crop treated (PCT) for all crops.
iii. Cancer. Based on the data summarized in the Fluazaindolizine
Human Health Risk Assessment, EPA has concluded that fluazaindolizine
does not pose a cancer risk to humans. Therefore, a dietary exposure
assessment for the purpose of assessing cancer risk is unnecessary.
iv. Anticipated residue and percent crop treated (PCT) information.
Section 408(b)(2)(E) of FFDCA authorizes EPA to use available data and
information on the anticipated residue levels of pesticide residues in
food and the actual levels of pesticide residues that have been
measured in food. If EPA relies on such information, EPA must require
pursuant to FFDCA section 408(f)(1) that data be provided 5 years after
the tolerance is established, modified, or left in effect,
demonstrating that the levels in food are not above the levels
anticipated. For the present action, EPA will issue such data call-ins
as are required by FFDCA section 408(b)(2)(E) and authorized under
FFDCA section 408(f)(1). Data will be required to be submitted no later
than 5 years from the date of issuance of these tolerances.
2. Dietary exposure from drinking water. The Agency used screening-
level water exposure models in the dietary exposure analysis and risk
assessment for fluazaindolizine in drinking water. Further information
regarding EPA drinking water models used in pesticide exposure
assessment can be found at http://www.epa.gov/pesticide-science-and-assessing-pesticide-risks/models-pesticide-risk-assessment.
Separate estimated drinking water concentrations (EDWCs) were
calculated for the metabolite IN-VM862 and a combination of
fluazaindolizine and the other metabolites IN-QEK31, IN-REG72, IN-
F4106, and IN-A5760, due to greater toxicological potency of IN-VM862.
This combination is referred to as the Fluazaindolizine Drinking Water
Total Residue Fraction (FDWTRF). Based on the Pesticide Water
Calculator (PWC), EPA used an EDWC of 990 ppb for FDWTRF and 1,300 ppb
for IN-VM862 in the chronic dietary risk assessment.
3. From non-dietary exposure. The term ``residential exposure'' is
used in this document to refer to non-occupational, non-dietary
exposure (e.g., for lawn and garden pest control, indoor pest control,
termiticides, and flea and tick control on pets). Fluazaindolizine is
not registered for any specific use patterns that would result in
residential exposure.
4. Cumulative effects from substances with a common mechanism of
toxicity. Section 408(b)(2)(D)(v) of FFDCA requires that, when
considering whether to establish, modify, or revoke a tolerance, the
Agency consider ``available information'' concerning the cumulative
effects of a particular pesticide's residues and ``other substances
that have a common mechanism of toxicity.''
Unlike other pesticides for which EPA has followed a cumulative
risk approach based on a common mechanism of toxicity, EPA has not made
a common mechanism of toxicity finding as to fluazaindolizine and any
other substances and fluazaindolizine does not appear to produce a
toxic metabolite produced by other substances. For the purposes of this
tolerance action, therefore, EPA has not assumed that fluazaindolizine
has a common mechanism of toxicity with other substances.
For information regarding EPA's efforts to determine which
chemicals have a common mechanism of toxicity and to evaluate the
cumulative effects of such chemicals, see EPA's website at https://www.epa.gov/pesticide-science-and-assessing-pesticide-risks/cumulative-assessment-risk-pesticides.
D. Safety Factor for Infants and Children
1. In general. 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.
2. Prenatal and postnatal sensitivity. Increased quantitative
susceptibility was observed for fluazaindolizine in the rat 2-
generation reproductive study. An increased incidence and severity of
urinary tract histopathology was observed in male and female
F2 weanlings at a lower dose than in P and F1
adult animals. No susceptibility was observed in the rat or rabbit
developmental toxicity studies. The metabolite IN-F4106 showed
increased prenatal susceptibility (decreased fetal body weight) in the
rat developmental toxicity study. However, concern for prenatal
susceptibility is low for both parent and metabolite because clear
NOAELs and LOAELs were identified for fetal toxicity and endpoints
selected for risk assessment are protective of these findings.
3. Conclusion. EPA has determined that reliable data show the
safety of infants and children would be adequately protected if the
FQPA SF were reduced to 1X. That decision is based on the following
findings:
i. The toxicity database for fluazaindolizine is complete.
ii. There is no indication that fluazaindolizine is a neurotoxic
chemical and there is no need for a developmental neurotoxicity study
or additional uncertainty factors to account for neurotoxicity.
iii. Increased quantitative susceptibility was observed for
fluazaindolizine in the rat two-generation reproductive study. However,
as noted above, concern for prenatal susceptibility is low for both
parent and metabolite because clear NOAELs and LOAELs were identified
for fetal toxicity and endpoints selected for risk assessment are
protective of these findings.
iv. There are no residual uncertainties with regard to the exposure
assessment
[[Page 62468]]
for fluazaindolizine. An acute dietary endpoint was not identified for
any population and therefore an assessment of acute dietary risk was
not performed. For chronic dietary exposure, risk estimates were
partially refined by using average field trial residues and empirical
processing factors. Conservative, upper bound estimates were used to
assess exposure to fluazaindolizine and its residues of concern through
drinking water. Based on these considerations, exposure from food and
drinking water will not be underestimated. No residential use patterns
are proposed at this time.
E. Aggregate Risks and Determination of Safety
EPA determines whether acute and chronic dietary pesticide
exposures are safe by comparing aggregate exposure estimates to the
acute PAD (aPAD) and chronic PAD (cPAD). For linear cancer risks, EPA
calculates the lifetime probability of acquiring cancer given the
estimated aggregate exposure. Short-, intermediate-, and chronic-term
risks are evaluated by comparing the estimated aggregate food, water,
and residential exposure to the appropriate PODs to ensure that an
adequate MOE exists.
1. Acute risk. An acute aggregate risk assessment takes into
account acute exposure estimates from dietary consumption of food and
drinking water. No adverse effect resulting from a single oral exposure
was identified and no acute dietary endpoint was selected. Therefore,
fluazaindolizine is not expected to pose an acute risk.
2. Chronic risk. Using the exposure assumptions described in this
unit for chronic exposure, EPA has concluded that chronic exposure to
fluazaindolizine from food and water will utilize 82% of the cPAD for
all infants less than one year old, the population group receiving the
greatest exposure. There are no residential uses for fluazaindolizine.
3. Short- and intermediate-term risk. Short- and intermediate-term
aggregate risk takes into account short- and intermediate-term
residential exposure plus chronic exposure to food and water
(considered to be a background exposure level). Short- and
intermediate-term adverse effects were identified; however,
fluazaindolizine is not registered for any use patterns that would
result in either short- or intermediate-term residential exposure.
Because there is no short- or intermediate-term residential exposure
and chronic dietary exposure has already been assessed under the
appropriately protective cPAD (which is at least as protective as the
POD used to assess short- or intermediate-term risk), no further
assessment of short- or intermediate-term risk is necessary, and EPA
relies on the chronic dietary risk assessment for evaluating short- and
intermediate-term risk for fluazaindolizine.
4. Aggregate cancer risk for U.S. population. Fluazaindolizine is
not expected to pose a cancer risk to humans.
5. Determination of safety. Based on these risk assessments, 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 fluazaindolizine residues.
IV. Other Considerations
A. Analytical Enforcement Methodology
Crops: The petitioner submitted method validation, supplemental
method validation, and radiovalidation data for Method No. DuPont-33861
(Rev. 3). This method successfully quantitates two ion transitions for
fluazaindolizine via liquid chromatography with tandem mass
spectrometry (LC-MS/MS). Method No. DuPont-33861 (Rev. 3) meets HED's
criteria for enforcement analytical methods.
Livestock: The petitioner submitted method validation and an
independent laboratory validation (ILV) for Method No. DuPont-39226
(Rev. 1). This method successfully quantitates two ion transitions for
fluazaindolizine via LC-MS/MS. Method No. DuPont-39226 (Rev. 1) meets
HED's criteria for enforcement analytical methods.
The methods 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).
The Codex has not established any MRLs for fluazaindolizine.
C. Response to Comments
One comment was received on the April 15, 2020, notice of filing
that stated in part ``this application should be denied. stop using
this chemical.'' Although the Agency recognizes that some individuals
believe that pesticides should be banned on agricultural crops, the
existing legal framework provided by section 408 of the FFDCA
authorizes EPA to establish tolerances when it determines that the
tolerance is safe. Upon consideration of the validity, completeness,
and reliability of the available data as well as other factors the
FFDCA requires EPA to consider, EPA has determined that the
fluazaindolizine tolerances are safe. The commenter has provided no
information indicating that a safety determination cannot be supported.
D. Revisions to Petitioned-For Tolerances
All tolerance values being established in this rulemaking vary
slightly from what the petitioner requested. This is primarily because
the petitioner proposed various metabolites as residues of concern for
crop and livestock commodities, whereas EPA has concluded that the only
residue needed to measure compliance with the tolerance is
fluazaindolizine. All raw agricultural commodity (RAC) crop tolerances
were calculated according to the Organization for Economic Cooperation
and Development (OECD) tolerance calculation procedure. Tolerances in/
on processed commodities were calculated by multiplying average
processing factors by the mean or highest average field trial (HAFT)
value for blended and non-blended commodities, respectively. Commodity
definitions are used in accordance with EPA's correct commodity
definition guideline.
EPA is not establishing the requested primary crop tolerances for
dried potato, potato process waste, tomato paste, and tomato puree, or
the requested rotational crop tolerances for aspirated grain fractions
(AGF), corn milled byproducts, soybean hulls, soybean meal, dehydrated
strawberries, and wheat milled byproducts. Residues of parent
fluazaindolizine in these processed commodities are not expected to
concentrate to levels above the associated tolerances for the raw
agricultural commodities, so processed commodity tolerances are not
necessary. The Agency is not establishing the requested primary crop
tolerance on tomato wet pomace, as this processed fraction is not
considered a significant feed item and a tolerance is not necessary.
The Agency is not establishing the requested rotational crop
tolerance for fruiting vegetable crop group 8-10, as residues of parent
fluazaindolizine are
[[Page 62469]]
expected to be below the limit of quantitation (LOQ) in fruiting
vegetables planted as rotational crops and therefore the primary crop
tolerance is adequate.
The Agency is not establishing the requested rotational crop
tolerances for the straw of commodities in crop groups 7 and 20, as
these are not identified as significant feed items and tolerances are
not needed. Similarly, EPA is not establishing the requested rotational
crop tolerance for the fodder of crop group 18, as this is not a
recognized commodity for the crop group.
Finally, EPA is establishing rotational crop tolerances for crop
groups 6-22, 7-22, 15-22 and 16-22 rather than the requested rotational
crop tolerances on crop groups 6, 7, 15 and 16. EPA proposed changes to
these four crop groups on January 10, 2022 (87 FR 1091) (FRL-5031-12-
OCSPP) and finalized the revised crop groups as 6-22, 7-22, 15-22 and
16-22 on September 21, 2022 (87 FR 57627) (FRL-5031-13-OCSPP). EPA
regulations state ``Once a revised crop group is established, EPA will
no longer establish tolerances under the pre-existing crop group.'' 40
CFR 180.40(j)(4). EPA has determined that the residue data support
rotational crop tolerances for crop groups 6-22, 7-22, 15-22 and 16-22
based on EPA's practice for evaluating residue data for rotational crop
tolerances and because there were no changes to major crops in groups
6-22, 7-22, 15-22 and 16-22. No food commodities are included in the
revised crop groups that were not already accounted for in the initial
dietary exposure assessment. Therefore, an updated dietary assessment
is not needed, and the exposure and risk assessments do not change as a
result of the crop group updates.
V. Conclusion
Therefore, tolerances are established for residues of
fluazaindolizine, including its metabolites and degradates in or on
carrot at 0.05 ppm; cattle, fat at 0.01 ppm; cattle, meat at 0.01 ppm;
cattle, meat byproducts at 0.01 ppm; egg at 0.01 ppm; goat, fat at 0.01
ppm; goat, meat at 0.01 ppm; goat, meat byproducts at 0.01 ppm; hog,
fat at 0.01 ppm; hog, meat at 0.01 ppm; hog, meat byproducts at 0.01
ppm; horse, fat at 0.01 ppm; horse, meat at 0.01 ppm; horse, meat
byproducts at 0.01 ppm; milk at 0.01 ppm; poultry, fat at 0.01 ppm;
poultry meat at 0.01 ppm; poultry, meat byproducts at 0.01 ppm; sheep,
fat at 0.01 ppm; sheep, meat at 0.01 ppm; sheep, meat byproducts at
0.01 ppm; tomato, dried at 0.4 ppm; vegetable, cucurbit, group 9 at
0.15 ppm; vegetable, fruiting, group 8-10 at 0.07 ppm; and vegetable,
tuberous and corm, subgroup 1C at 0.2 ppm.
Additionally, tolerances are established for inadvertent residues
of fluazaindolizine, including its metabolites and degradates in or on
animal feed, nongrass, group 18, forage at 0.01 ppm; animal feed,
nongrass, group 18, hay at 0.015 ppm; animal feed, nongrass, group 18,
straw at 0.15 ppm; berry, low growing, subgroup 13-07G at 0.01 ppm;
grain, cereal, forage, hay, stover, and straw group 16-22, forage at
0.01 ppm; grain, cereal, forage, hay, stover, and straw group 16-22,
hay at 0.015 ppm; grain, cereal, forage, hay, stover, and straw group
16-22, stover at 0.15 ppm; grain, cereal, forage, hay, stover, and
straw group 16-22, straw at 0.15 ppm; grain, cereal, group 15-22 at
0.01 ppm; grass, forage, fodder and hay, group 17, forage at 0.01 ppm;
grass, forage, fodder, and hay, group 17, hay at 0.015 ppm; grass,
forage, fodder and hay, group 17, straw at 0.15 ppm; oilseed group 20
at 0.8 ppm; rapeseed, forage at 0.09 ppm; stalk, stem, and leaf petiole
vegetable group 22 at 0.03 ppm; vegetable, Brassica, head and stem,
group 5-16 at 0.015 ppm; vegetable, bulb, group 3-07 at 0.03 ppm;
vegetable, legume, forage and hay, group 7-22, forage at 0.09 ppm;
vegetable, legume, forage and hay, group 7-22, hay at 0.4 ppm;
vegetable, leafy, group 4-16 at 0.015 ppm; vegetable, leaves of root
and tuber, group 2 at 0.015 ppm; vegetable, legume, group 6-22 at 0.8
ppm; and vegetable, root, subgroup 1B at 0.02 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 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 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
[[Page 62470]]
and pests, Reporting and recordkeeping requirements.
Dated: September 5, 2023.
Edward Messina,
Director, 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. Add Sec. 180.720 to subpart C to read as follows:
Sec. 180.720 Fluazaindolizine; tolerances for residues.
(a) General. Tolerances are established for residues of the
nematicide fluazaindolizine, including its metabolites and degradates,
in or on the commodities to Table 1 of this section. Compliance with
the tolerance levels specified in Table 1 is to be determined by
measuring only fluazaindolizine, 8-chloro-N-[(2-chloro-5-
methoxyphenyl)sulfonyl]-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-
carboxamide, in or on the commodity.
Table 1 to Paragraph (a)
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
Carrot.................................................. 0.05
Cattle, fat............................................. 0.01
Cattle, meat............................................ 0.01
Cattle, meat byproducts................................. 0.01
Egg..................................................... 0.01
Goat, fat............................................... 0.01
Goat, meat.............................................. 0.01
Goat, meat byproducts................................... 0.01
Hog, fat................................................ 0.01
Hog, meat............................................... 0.01
Hog, meat byproducts.................................... 0.01
Horse, fat.............................................. 0.01
Horse, meat............................................. 0.01
Horse, meat byproducts.................................. 0.01
Milk.................................................... 0.01
Poultry, fat............................................ 0.01
Poultry, meat........................................... 0.01
Poultry, meat byproducts................................ 0.01
Sheep, fat.............................................. 0.01
Sheep, meat............................................. 0.01
Sheep, meat byproducts.................................. 0.01
Tomato, dried........................................... 0.4
Vegetable, cucurbit, group 9............................ 0.15
Vegetable, fruiting, group 8-10......................... 0.07
Vegetable, tuberous and corm, subgroup 1C............... 0.2
------------------------------------------------------------------------
(b)-(c) [Reserved]
(d) Indirect or inadvertent residues. Tolerances are established
for residues of the nematicide fluazaindolizine, including its
metabolites and degradates, in or on the commodities to Table 2 of this
section. Compliance with the tolerance levels specified in Table 2 is
to be determined by measuring only fluazaindolizine, 8-chloro-N-[(2-
chloro-5-methoxyphenyl)sulfonyl]-6-(trifluoromethyl)imidazo[1,2-
a]pyridine-2-carboxamide, in or on the commodity.
Table 2 to Paragraph (d)
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
Animal feed, nongrass, group 18, forage................. 0.01
Animal feed, nongrass, group 18, hay.................... 0.015
Animal feed, nongrass, group 18, straw.................. 0.15
Berry, low growing, subgroup 13-07G..................... 0.01
Grain, cereal, forage, hay, stover, and straw group 16- 0.01
22, forage.............................................
Grain, cereal, forage, hay, stover, and straw group 16- 0.015
22, hay................................................
Grain, cereal, forage, hay, stover, and straw group 16- 0.15
22, stover.............................................
Grain, cereal, forage, hay, stover, and straw group 16- 0.15
22, straw..............................................
Grain, cereal, group 15-22.............................. 0.01
Grass, forage, fodder and hay, group 17, forage......... 0.01
Grass, forage, fodder and hay, group 17, hay............ 0.015
Grass, forage, fodder and hay, group 17, straw.......... 0.15
Oilseed group 20........................................ 0.8
Rapeseed, forage........................................ 0.09
Stalk, stem and leaf petiole vegetable group 22......... 0.03
[[Page 62471]]
Vegetable, Brassica, head and stem, group 5-16.......... 0.015
Vegetable, bulb, group 3-07............................. 0.03
Vegetable, legume, forage and hay, group 7-22, forage... 0.09
Vegetable, legume, forage and hay, group 7-22, hay...... 0.4
Vegetable, leafy, group 4-16............................ 0.015
Vegetable, leaves of root and tuber, group 2............ 0.015
Vegetable, legume, group 6-22........................... 0.8
Vegetable, root, subgroup 1B............................ 0.02
------------------------------------------------------------------------
[FR Doc. 2023-19607 Filed 9-11-23; 8:45 am]
BILLING CODE 6560-50-P