Oxirane, 2-methyl-, Polymer With Oxirane, Monoundecyl Ether, Branched and Linear; Exemption From the Requirement of a Tolerance, 44712-44718 [2019-18362]
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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).
§ 180.350 Nitrapyrin; tolerances for
residues.
(a) General. Tolerances are
established for residues of the
nitrification inhibitor nitrapyrin,
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 nitrapyrin (2-chloro-6(trichloromethyl) pyridine) and its 6–
CPA metabolite (6-chloro-picolinic
acid), calculated as the stoichiometric
equivalent of nitrapyrin, in or on the
commodity:
Parts per
million
Commodity
*
*
*
*
Fruit, citrus, group 10–10 ...........
Fruit, citrus, group 10–10, dried
pulp .........................................
Fruit, citrus, group 10–10, oil ......
Leaf petiole vegetable subgroup
22B ..........................................
*
0.06
*
*
*
*
Vegetable, Brassica, head and
stem, group 5–16 ....................
Vegetable, bulb, group 3–07 ......
Vegetable, leafy, group 4–16 .....
*
*
*
*
*
*
*
*
0.5
2
0.5
0.1
0.3
0.4
*
*
*
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
[FR Doc. 2019–18382 Filed 8–26–19; 8:45 am]
Dated: August 8, 2019.
Michael Goodis,
Director, Registration Division, Office of
Pesticide Programs.
40 CFR Part 180
Environmental Protection
Agency (EPA).
ACTION: Final rule.
1. The authority citation for part 180
continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.350, paragraph (a):
a. Revise the introductory text.
b. Add alphabetically the entries for
‘‘Fruit, citrus, group 10–10’’; ‘‘Fruit,
citrus, group 10–10, dried pulp’’; ‘‘Fruit,
■
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This regulation establishes an
exemption from the requirement of a
tolerance for residues of oxirane, 2methyl-, polymer with oxirane,
monoundecyl ether, branched and
linear (CAS Reg. No. 2222805–23–2)
SUMMARY:
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when used as an inert ingredient in a
pesticide chemical formulation.
Exponent, Inc. on behalf of Clariant
Corporation submitted a petition to EPA
under the Federal Food, Drug, and
Cosmetic Act (FFDCA), requesting an
amendment to an existing requirement
of a tolerance. This regulation
eliminates the need to establish a
maximum permissible level for residues
of oxirane, 2-methyl-, polymer with
oxirane, monoundecyl ether, branched
and linear.
DATES: This regulation is effective
August 27, 2019. Objections and
requests for hearings must be received
on or before October 28, 2019, 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–2019–0093, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Michael Goodis, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; main telephone number:
(703) 305–7090; email address:
RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
AGENCY:
■
17:38 Aug 26, 2019
ENVIRONMENTAL PROTECTION
AGENCY
Oxirane, 2-methyl-, Polymer With
Oxirane, Monoundecyl Ether,
Branched and Linear; Exemption From
the Requirement of a Tolerance
PART 180—[AMENDED]
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BILLING CODE 6560–50–P
[EPA–HQ–OPP–2019–0093; FRL–9996–95]
Therefore, 40 CFR chapter I is
amended as follows:
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citrus, group 10–10, oil’’; ‘‘Leaf petiole
vegetable subgroup 22B’’; ‘‘Vegetable,
Brassica, head and stem, group 5–16’’;
‘‘Vegetable, bulb, group 3–07’’; and
‘‘Vegetable, leafy, group 4–16’’ to the
table.
The revision and additions read as
follows:
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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).
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• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
available at https://www.epa.gov/
dockets.
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of 40 CFR part 180
through the Government Publishing
Office’s e-CFR site at https://
www.ecfr.gov/cgi-bin/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl.
In the Federal Register of August 5,
2009 (74 FR 38935) (FRL–8430–1), EPA
issued a final rule, announcing the
establishment of a tolerance exemption
pursuant to a pesticide petition (PP
9E7534) by The Joint Inerts Task Force,
Cluster Support Team 1 (CST 1), c/o
CropLife America, 1156 15th Street NW,
Suite 400, Washington, DC 20005. The
petition requested that 40 CFR 180.910,
180.930, 180.940(a) and 180.960 be
amended by establishing an exemption
from the requirement of a tolerance for
residues of a group of substances known
as a-alkyl-whydroxypoly(oxypropylene) and/or poly
(oxyethylene) polymers where the alkyl
chain contains a minimum of 6 carbons,
herein referred to in this document as
AAA.
The current petition seeks to expand
the exemptions for AAA by adding
additional CAS Reg. Nos. In the Federal
Register of May 13, 2019 (84 FR 20843)
(FRL–9991–91), EPA issued a document
pursuant to FFDCA section 408, 21
U.S.C. 346a, announcing the filing of a
pesticide petition (PP IN–11254) by
Exponent Inc. on behalf of Clariant
Corporation, Suite 1100, 1150
Connecticut Avenue NW, Washington
DC 20036. The petition requested that
40 CFR 180.910, 180.930, 180.940(a)
and 180.960 be amended by establishing
an exemption from the requirement of a
tolerance for residues of oxirane,
2-methyl-, polymer with oxirane,
monoundecyl ether, branched and
linear (CAS Reg. No. 2222805–23–2).
That document referenced a summary of
the petition prepared by Exponent, the
petitioner, 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 has
confirmed that the requested CAS Reg.
No. is acceptable for consideration
under the currently approved
descriptor. This determination is based
on the Agency’s risk assessment which
can be found at https://
www.regulations.gov in document
‘‘Alkyl Alcohol Alkoxylates (AAA–JITF
CST 1 Inert Ingredient), Human Health
Risk Assessment to Support Proposed
Exemption from the Requirement of a
Tolerance under 40 CFR 180.960 when
used as an Inert Ingredient in Pesticide
Formulations’’ in docket ID number
EPA–HQ–OPP–2009–0145.
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–2019–0093 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 28, 2019. 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–
2019–0093, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be CBI or
other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW, Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on commenting
or visiting the docket, along with more
information about dockets generally, is
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II. Petition for Exemption
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III. Inert Ingredient Definition
Inert ingredients are all ingredients
that are not active ingredients as defined
in 40 CFR 153.125 and include, but are
not limited to, the following types of
ingredients (except when they have a
pesticidal efficacy of their own):
Solvents such as alcohols and
hydrocarbons; surfactants such as
polyoxyethylene polymers and fatty
acids; carriers such as clay and
diatomaceous earth; thickeners such as
carrageenan and modified cellulose;
wetting, spreading, and dispersing
agents; propellants in aerosol
dispensers; microencapsulating agents;
and emulsifiers. The term ‘‘inert’’ is not
intended to imply nontoxicity; the
ingredient may or may not be
chemically active. Generally, EPA has
exempted inert ingredients from the
requirement of a tolerance based on the
low toxicity of the individual inert
ingredients.
IV. Aggregate Risk Assessment and
Determination of Safety
Section 408(c)(2)(A)(i) of FFDCA
allows EPA to establish an exemption
from the requirement for 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. . . .’’
EPA establishes exemptions from the
requirement of a tolerance only in those
cases where it can be clearly
demonstrated that the risks from
aggregate exposure to pesticide
chemical residues under reasonably
foreseeable circumstances will pose no
appreciable risks to human health. In
order to determine the risks from
aggregate exposure to pesticide inert
ingredients, the Agency considers the
toxicity of the inert in conjunction with
possible exposure to residues of the
inert ingredient through food, drinking
water, and through other exposures that
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occur as a result of pesticide use in
residential settings. If EPA is able to
determine that a finite tolerance is not
necessary to ensure that there is a
reasonable certainty that no harm will
result from aggregate exposure to the
inert ingredient, an exemption from the
requirement of a tolerance may be
established.
Consistent with FFDCA section
408(c)(2)(A), and the factors specified in
FFDCA section 408(c)(2)(B), 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 oxirane, 2methyl-, polymer with oxirane,
monoundecyl ether, branched and
linear including exposure resulting from
the exemption established by this
action. EPA’s assessment of exposures
and risks associated with oxirane, 2methyl-, polymer with oxirane,
monoundecyl ether, branched and
linear follows.
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A. Toxicological Profile
EPA has evaluated the available
toxicity data and considered their
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. Specific
information on the studies received and
the nature of the adverse effects caused
by AAA as well as the no-observedadverse-effect-level (NOAEL) and the
lowest-observed-adverse-effect-level
(LOAEL) from the toxicity studies are
discussed in the final rule published in
the Federal Register of August 5, 2009
(74 FR 38935) (FRL–8430–1).
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
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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 https://
www.epa.gov/pesticides/factsheets/
riskassess.htm.
A summary of the toxicological
endpoints for AAA used for human risk
assessment is discussed in Unit IV of
the final rule published in the Federal
Register of August 5, 2009 (74 FR
38938) (FRL–8430–1).
C. Exposure Assessment
1. Dietary exposure from food and
feed uses. In evaluating dietary
exposure to AAA, EPA considered
exposure under the proposed exemption
from the requirement of a tolerance.
EPA assessed dietary exposures from
AAA in food as follows:
i. Acute exposure. No adverse effects
attributable to a single exposure of the
AAAs was seen in the toxicity
databases. Therefore, acute dietary risk
assessments for the AAAs are not
necessary.
ii. Chronic exposure. In conducting
the chronic dietary exposure
assessment, EPA used food
consumption information from the U.S.
Department of Agriculture (USDA) 1994
-1996 and 1998 Nationwide Continuing
Surveys of Food Intake by Individuals
(CSFII).
iii. Cancer. The Agency used a
qualitative structure activity
relationship (SAR) database, DEREK11,
to determine if there were structural
alerts suggestive of carcinogenicity. No
structural alerts for carcinogenicity were
identified. The AAAs are not expected
to be carcinogenic. Therefore, a cancer
dietary exposure assessment is not
necessary to assess cancer risk.
2. Dietary exposure from drinking
water. The Agency used screening level
water exposure models in the dietary
exposure analysis and risk assessment
for the AAAs in drinking water.
3. From non-dietary exposure. The
term ‘‘residential exposure’’ is used in
this document to refer to
nonoccupational, non-dietary exposure
(e.g., for lawn and garden pest control,
indoor pest control, termiticides, and
flea and tick control on pets). The AAAs
may be used in inert ingredients in
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pesticide products that are registered for
specific uses that may result in both
indoor and outdoor residential
exposures. A screening level residential
exposure and risk assessment was
completed for products containing the
AAAs as inert ingredients.
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.’’
EPA has not found AAA to share a
common mechanism of toxicity with
any other substances, and AAA does not
appear to produce a toxic metabolite
produced by other substances. For the
purposes of this tolerance action,
therefore, EPA has assumed that AAA
does not have 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/pesticides/cumulative.
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.
In the case of the lower weight AAA
surfactants, there was no evidence of
increased susceptibility to the offspring
of rats following prenatal and postnatal
exposure in the reproductive/
developmental screening studies on
several representative AAA surfactants.
Decreased litter size and increased postimplantation loss were observed in one
OPPTS Harmonized Guideline 870.3550
reproduction/developmental toxicity
screening study at 470 mg/kg/day where
maternal/paternal toxicity was
manifested as one maternal death (GD
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22), decreased body weight, bodyweight
gain and food consumption and clinical
signs (ptosis and hypoactivity) and
microscopic changes in the testes
(atrophy) and epididymides (increased
intraluminal exfoliated spermatogenic
cells) and dilated seminiferous tubules
at the same dose (470 mg/kg/day). The
maternal and offspring toxicity NOAEL
was 168 mg/kg/day. The offspring
toxicity in the OPPTS Harmonized Test
Guideline 870.3650 study was
manifested in the presence of more
severe maternal toxicity (deaths),
therefore, EPA concluded that there is
no evidence of increased susceptibility
in this study. In addition, there was no
evidence of increased susceptibility in
other submitted studies.
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 for the lower weight
AAAs. (As discussed earlier, given the
low toxicological concerns with the
high weight AAAs, a safety factor
analysis is unnecessary).
E. Aggregate Risks and Determination of
Safety Determination of Safety Section
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, AAA is not
expected to pose an acute risk.
2. Chronic risk. A chronic aggregate
risk assessment takes into account
exposure estimates from chronic dietary
consumption of food and drinking
water. Using the exposure assumptions
discussed in this unit for chronic
exposure the chronic dietary exposure
from food and water to the AAAs is
11% of the cPAD for the U.S.
population and 37% of the cPAD for
children 1 to 2 years old, the most
highly exposed population subgroup.
3. Short-term risk. Short-term
aggregate exposure takes into account
short-term residential exposure plus
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chronic exposure to food and water
(considered to be a background
exposure level).
AAAs are used as inert ingredients in
pesticide products that are currently
registered for uses that could result in
short-term residential exposure and the
Agency has determined that it is
appropriate to aggregate chronic
exposure through food and water with
short-term residential exposures to the
AAAs. EPA has concluded that the
combined short-term aggregated food,
water, and residential exposures result
in aggregate MOEs of 110 for both adult
males and females. Adult residential
exposure combines high end indoor
inhalation handler exposure with a
high-end post application to pet
exposures. EPA has concluded the
combined short-term aggregated food,
water, and residential exposures result
in an aggregate MOE of 110 for children.
Children’s residential exposure includes
total combined pet exposures. As the
level of concern is for MOEs that are
lower than 100, these MOEs are not of
concern.
4. Intermediate-term risk.
Intermediate-term aggregate exposure
takes into account intermediate-term
residential exposure plus chronic
exposure to food and water (considered
to be a background exposure level).
The AAAs are used as inert
ingredients in pesticide products that
are currently registered for uses that
could result in intermediate-term
residential exposure and the Agency has
determined that it is appropriate to
aggregate chronic exposure through food
and water with intermediate-term
residential exposures to the AAAs. EPA
has concluded that the combined
intermediate-term aggregated food,
water, and residential exposures result
in aggregate MOEs of 230 for both adult
males and females, respectively. Adult
residential exposure includes high-end
post application dermal exposure from
contact with treated pets. EPA has
concluded that the combined
intermediate-term aggregated food,
water, and residential exposures result
in an aggregate MOE of 110 for children.
Children’s residential exposure includes
total combined pet exposure. As the
level of concern is for MOEs that are
lower than 100, these MOEs are not of
concern.
5. Aggregate cancer risk for U.S.
population. The Agency has not
identified any concerns for
carcinogenicity relating to the AAAs.
6. 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
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from aggregate exposure to residues of
the lower weight AAAs. For the high
molecular weight AAAs under 40 CFR
180.960. Since AAA conforms to the
criteria that identify a low-risk polymer,
there are no concerns for risks
associated with any potential exposure
scenarios that are reasonably
foreseeable. Therefore, 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 residues of
the high molecular weight AAAs.
V. Other Considerations
A. Analytical Enforcement Methodology
An analytical method is not required
for enforcement purposes since the
Agency is establishing an exemption
from the requirement of a tolerance
without any numerical limitation.
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 Nation 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 AAAs.
VI. Conclusions
Therefore, an exemption from the
requirement of a tolerance is established
for residues of the lower molecular
weight a-alkyl-whydroxypoly(oxypropylene) and/or poly
(oxyethylene) polymers where the alkyl
chain contains a minimum of 6 carbons,
including oxirane, 2-methyl-, polymer
with oxirane, monoundecyl ether,
branched and linear (CAS Reg. No.
2222805–23–2) when used as an inert
ingredient in pesticide formulations
applied to pre- and post-harvest,
applied to livestock, and used in
antimicrobial formulations under 40
CFR 180.910, 40 CFR 180.930, and 40
CFR 180.940(a). In addition, an
E:\FR\FM\27AUR1.SGM
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Federal Register / Vol. 84, No. 166 / Tuesday, August 27, 2019 / Rules and Regulations
exemption from the requirement of a
tolerance is established for residues of
the larger molecular weight compounds
of a-alkyl-w-hydroxypoly
(oxypropylene) and/or poly
(oxyethylene) polymers where the alkyl
chain contains a minimum of 6 carbons,
including oxirane, 2-methyl-, polymer
with oxirane, monoundecyl ether,
branched and linear (CAS Reg. No.
2222805–23–2) under 40 CFR 180.960.
jspears on DSK3GMQ082PROD with RULES
VII. 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).
VIII. 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: August 16, 2019.
Daniel Rosenblatt,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.910, revise the inert
ingredients ‘‘a-Alkyl-w-hydroxypoly
(oxypropylene) and/or poly
(oxyethylene) polymers where the alkyl
chain contains a minimum of six
carbons’’ in the table to read as follows:
■
§ 180.910 Inert ingredients used pre- and
post-harvest; exemptions from the
requirement of a tolerance.
*
*
*
*
*
Inert ingredients
Limits
*
*
*
*
*
*
a-Alkyl-w-hydroxypoly (oxypropylene) and/or poly (oxyethylene) polymers where the alkyl chain contains a minimum of six carbons
(CAS Reg. Nos.: 9002–92–0; 9004–95–9; 9004–98–2; 9005–00–9; 9035–85–2; 9038–29–3; 9038–43–1; 9040–05–5; 9043–30–5;
9087–53–0; 25190–05–0; 24938–91–8; 25231–21–4; 251553–55–6; 26183–52–8; 26468–86–0; 26636–39–5; 27252–75–1;
27306–79–2; 31726–34–8; 34398–01–1; 34398–05–5; 37251–67–5; 37311–00–5; 37311–01–6; 37311–02–7; 37311–04–9;
39587–22–9; 50861–66–0; 52232–09–4; 52292–17–8; 52609–19–5; 57679–21–7; 59112–62–8; 60828–78–6; 61702–78–1;
61723–78–2; 61725–89–1; 61791–13–7; 61791–20–6; 61791–28–4; 61804–34–0; 61827–42–7; 61827–84–7; 62648–50–4;
63303–01–5; 63658–45–7; 63793–60–2; 64366–70–7; 64415–24–3; 64415–25–4; 64425–86–1; 65104–72–5; 65150–81–4;
66455–14–9: 66455–15–0; 67254–71–1; 67763–08–0; 68002–96–0; 68002–97–1; 68131–39–5; 68131–40–8; 68154–96–1;
68154–97–2; 68154–98–3; 68155–01–1; 68213–23–0; 68213–24–1; 68238–81–3; 68238–82–4; 68409–58–5; 68409–59–6;
68439–30–5; 68439–45–2; 68439–46–3; 68439–48–5; 68439–49–6; 68439–50–9; 68439–51–0; 68439–53–2; 68439–54–3;
68458–88–8; 68526–94–3; 68526–95–4; 68551–12–2; 68551–13–3; 68551–14–4; 68603–20–3; 68603–25–8; 68920–66–1;
68920–69–4; 68937–66–6; 68951–67–7; 68954–94–9; 68987–81–5; 68991–48–0; 69011–36–5; 69013–18–9; 69013–19–0;
69227–20–9; 69227–21–0; 69227–22–1; 69364–63–2; 70750–27–5; 70879–83–3; 70955–07–6; 71011–10–4; 71060–57–6;
71243–46–4; 72066–65–0; 72108–90–8; 72484–69–6; 72854–13–8; 72905–87–4; 73018–31–2; 73049–34–0; 74432–13–6;
74499–34–6; 78330–19–5; 78330–20–8; 78330–21–9; 78330–23–1; 79771–03–2; 84133–50–6; 85422–93–1; 97043–91–9;
97953–22–5; 102782–43–4; 103331–86–8; 103657–84–7; 103657–85–8; 103818–93–5; 103819–03–0; 106232–83–1; 111905–
54–5; 116810–31–2; 116810–32–3; 116810–33–4; 120313–48–6; 120944–68–5; 121617–09–2; 126646–02–4; 126950–62–7;
127036–24–2; 139626–71–4; 152231–44–2; 154518–36–2; 157627–86–6; 157627–88–8; 157707–41–0; 157707–43–2; 159653–
49–3; 160875–66–1; 160901–20–2; 160901–09–7; 160901–19–9; 161025–21–4; 161025–22–5; 166736–08–9; 169107–21–5;
172588–43–1; 176022–76–7; 196823–11–7; 287935–46–0; 288260–45–7; 303176–75–2; 954108–36–2; 2222805–23–2).
*
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3. In § 180.930, revise the inert
ingredients ‘‘a-Alkyl-w-hydroxypoly
(oxypropylene) and/or poly
(oxyethylene) polymers where the alkyl
■
chain contains a minimum of six
carbons’’ in the table to read as follows:
§ 180.930 Inert ingredients applied to
animals; exemptions from the requirement
of a tolerance.
*
*
*
*
Inert ingredients
*
Limits
*
*
*
*
*
*
a-Alkyl-w-hydroxypoly (oxypropylene) and/or poly (oxyethylene) polymers where the alkyl chain contains a min- ....................
imum of six carbons (CAS Reg. Nos.: 9002–92–0; 9004–95–9; 9004–98–2; 9005–00–9; 9035–85–2; 9038–29–
3; 9038–43–1; 9040–05–5; 9043–30–5; 9087–53–0; 25190–05–0; 24938–91–8; 25231–21–4; 251553–55–6;
26183–52–8; 26468–86–0; 26636–39–5; 27252–75–1; 27306–79–2; 31726–34–8; 34398–01–1; 34398–05–5;
37251–67–5; 37311–00–5; 37311–01–6; 37311–02–7; 37311–04–9; 39587–22–9; 50861–66–0; 52232–09–4;
52292–17–8; 52609–19–5; 57679–21–7; 59112–62–8; 60828–78–6; 61702–78–1; 61723–78–2; 61725–89–1;
61791–13–7; 61791–20–6; 61791–28–4; 61804–34–0; 61827–42–7; 61827–84–7; 62648–50–4; 63303–01–5;
63658–45–7; 63793–60–2; 64366–70–7; 64415–24–3; 64415–25–4; 64425–86–1; 65104–72–5; 65150–81–4;
66455–14–9: 66455–15–0; 67254–71–1; 67763–08–0; 68002–96–0; 68002–97–1; 68131–39–5; 68131–40–8;
68154–96–1; 68154–97–2; 68154–98–3; 68155–01–1; 68213–23–0; 68213–24–1; 68238–81–3; 68238–82–4;
68409–58–5; 68409–59–6; 68439–30–5; 68439–45–2; 68439–46–3; 68439–48–5; 68439–49–6; 68439–50–9;
68439–51–0; 68439–53–2; 68439–54–3; 68458–88–8; 68526–94–3; 68526–95–4; 68551–12–2; 68551–13–3;
68551–14–4; 68603–20–3; 68603–25–8; 68920–66–1; 68920–69–4; 68937–66–6; 68951–67–7; 68954–94–9;
68987–81–5; 68991–48–0; 69011–36–5; 69013–18–9; 69013–19–0; 69227–20–9; 69227–21–0; 69227–22–1;
69364–63–2; 70750–27–5; 70879–83–3; 70955–07–6; 71011–10–4; 71060–57–6; 71243–46–4; 72066–65–0;
72108–90–8; 72484–69–6; 72854–13–8; 72905–87–4; 73018–31–2; 73049–34–0; 74432–13–6; 74499–34–6;
78330–19–5; 78330–20–8; 78330–21–9; 78330–23–1; 79771–03–2; 84133–50–6; 85422–93–1; 97043–91–9;
97953–22–5; 102782–43–4; 103331–86–8; 103657–84–7; 103657–85–8; 103818–93–5; 103819–03–0;
106232–83–1; 111905–54–5; 116810–31–2; 116810–32–3; 116810–33–4; 120313–48–6; 120944–68–5;
121617–09–2; 126646–02–4; 126950–62–7; 127036–24–2; 139626–71–4; 152231–44–2; 154518–36–2;
157627–86–6; 157627–88–8; 157707–41–0; 157707–43–2; 159653–49–3; 160875–66–1; 160901–20–2;
160901–09–7; 160901–19–9; 161025–21–4; 161025–22–5; 166736–08–9; 169107–21–5; 172588–43–1;
176022–76–7; 196823–11–7; 287935–46–0; 288260–45–7; 303176–75–2; 954108–36–2; 2222805–23–2).
*
*
*
4. In § 180.940, revise the inert
ingredients ‘‘a-Alkyl-w-hydroxypoly
(oxypropylene) and/or poly
(oxyethylene) polymers where the alkyl
chain contains a minimum of six
jspears on DSK3GMQ082PROD with RULES
■
*
*
carbons’’ in the table in paragraph (a) to
read as follows:
*
§ 180.940 Tolerance exemptions for active
and inert ingredients for use in
antimicrobial formulations (Food-contact
surface sanitizing solutions).
*
*
*
(a) * * *
*
*
CAS Reg. No.
*
a-Alkyl-w-hydroxypoly
(oxypropylene) and/or
poly (oxyethylene) polymers where the alkyl
chain contains a minimum of six carbons.
*
*
*
*
*
9002–92–0; 9004–95–9; 9004–98–2; 9005–00–9; 9035–85–2; 9038–29–3; 9038–43–1; 9040–05–5;
9043–30–5; 9087–53–0; 25190–05–0; 24938–91–8; 25231–21–4; 251553–55–6; 26183–52–8;
26468–86–0; 26636–39–5; 27252–75–1; 27306–79–2; 31726–34–8; 34398–01–1; 34398–05–5;
37251–67–5; 37311–00–5; 37311–01–6; 37311–02–7; 37311–04–9; 39587–22–9; 50861–66–0;
52232–09–4; 52292–17–8; 52609–19–5; 57679–21–7; 59112–62–8; 60828–78–6; 61702–78–1;
61723–78–2; 61725–89–1; 61791–13–7; 61791–20–6; 61791–28–4; 61804–34–0; 61827–42–7;
61827–84–7; 62648–50–4; 63303–01–5; 63658–45–7; 63793–60–2; 64366–70–7; 64415–24–3;
64415–25–4; 64425–86–1; 65104–72–5; 65150–81–4; 66455–14–9: 66455–15–0; 67254–71–1;
67763–08–0; 68002–96–0; 68002–97–1; 68131–39–5; 68131–40–8; 68154–96–1; 68154–97–2;
68154–98–3; 68155–01–1; 68213–23–0; 68213–24–1; 68238–81–3; 68238–82–4; 68409–58–5;
68409–59–6; 68439–30–5; 68439–45–2; 68439–46–3; 68439–48–5; 68439–49–6; 68439–50–9;
68439–51–0; 68439–53–2; 68439–54–3; 68458–88–8; 68526–94–3; 68526–95–4; 68551–12–2;
68551–13–3; 68551–14–4; 68603–20–3; 68603–25–8; 68920–66–1; 68920–69–4; 68937–66–6;
68951–67–7; 68954–94–9; 68987–81–5; 68991–48–0; 69011–36–5; 69013–18–9; 69013–19–0;
69227–20–9; 69227–21–0; 69227–22–1; 69364–63–2; 70750–27–5; 70879–83–3; 70955–07–6;
71011–10–4; 71060–57–6; 71243–46–4; 72066–65–0; 72108–90–8; 72484–69–6; 72854–13–8;
72905–87–4; 73018–31–2; 73049–34–0; 74432–13–6; 74499–34–6; 78330–19–5; 78330–20–8;
78330–21–9; 78330–23–1; 79771–03–2; 84133–50–6; 85422–93–1; 97043–91–9; 97953–22–5;
102782–43–4; 103331–86–8; 103657–84–7; 103657–85–8; 103818–93–5; 103819–03–0; 106232–
83–1; 111905–54–5; 116810–31–2; 116810–32–3; 116810–33–4; 120313–48–6; 120944–68–5;
121617–09–2; 126646–02–4; 126950–62–7; 127036–24–2; 139626–71–4; 152231–44–2; 154518–
36–2; 157627–86–6; 157627–88–8; 157707–41–0; 157707–43–2; 159653–49–3; 160875–66–1;
160901–20–2; 160901–09–7; 160901–19–9; 161025–21–4; 161025–22–5; 166736–08–9; 169107–
21–5; 172588–43–1; 176022–76–7; 196823–11–7; 287935–46–0; 288260–45–7; 303176–75–2;
954108–36–2; 2222805–23–2.
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*
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related adjuvants of
surfactants
*
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*
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None
*
44718
*
Federal Register / Vol. 84, No. 166 / Tuesday, August 27, 2019 / Rules and Regulations
*
*
*
*
(oxyethylene) polymers where the alkyl
chain contains a minimum of six
carbons and a minimum number
average molecular weight (in amu)
1,100’’ in the table to read as follows:
5. In § 180.960, revise the inert
ingredients ‘‘a-Alkyl-w-hydroxypoly
(oxypropylene) and/or poly
■
Polymer
§ 180.960 Polymers; exemptions from the
requirement of a tolerance.
*
*
*
*
*
CAS No.
*
*
*
*
*
*
*
a-Alkyl-w-hydroxypoly
9002–92–0; 9004–95–9; 9004–98–2; 9005–00–9; 9035–85–2; 9038–29–3; 9038–43–1; 9040–05–5; 9043–30–5;
(oxypropylene) and/or poly
9087–53–0; 25190–05–0; 24938–91–8; 25231–21–4; 251553–55–6; 26183–52–8; 26468–86–0; 26636–39–5;
(oxyethylene) polymers
27252–75–1; 27306–79–2; 31726–34–8; 34398–01–1; 34398–05–5; 37251–67–5; 37311–00–5; 37311–01–6;
where the alkyl chain con37311–02–7; 37311–04–9; 39587–22–9; 50861–66–0; 52232–09–4; 52292–17–8; 52609–19–5; 57679–21–7;
tains a minimum of six
59112–62–8; 60828–78–6; 61702–78–1; 61723–78–2; 61725–89–1; 61791–13–7; 61791–20–6; 61791–28–4;
carbons and a minimum
61804–34–0; 61827–42–7; 61827–84–7; 62648–50–4; 63303–01–5; 63658–45–7; 63793–60–2; 64366–70–7;
number average molecular
64415–24–3; 64415–25–4; 64425–86–1; 65104–72–5; 65150–81–4; 66455–14–9: 66455–15–0; 67254–71–1;
weight (in amu) 1,100.
67763–08–0; 68002–96–0; 68002–97–1; 68131–39–5; 68131–40–8; 68154–96–1; 68154–97–2; 68154–98–3;
68155–01–1; 68213–23–0; 68213–24–1; 68238–81–3; 68238–82–4; 68409–58–5; 68409–59–6; 68439–30–5;
68439–45–2; 68439–46–3; 68439–48–5; 68439–49–6; 68439–50–9; 68439–51–0; 68439–53–2; 68439–54–3;
68458–88–8; 68526–94–3; 68526–95–4; 68551–12–2; 68551–13–3; 68551–14–4; 68603–20–3; 68603–25–8;
68920–66–1; 68920–69–4; 68937–66–6; 68951–67–7; 68954–94–9; 68987–81–5; 68991–48–0; 69011–36–5;
69013–18–9; 69013–19–0; 69227–20–9; 69227–21–0; 69227–22–1; 69364–63–2; 70750–27–5; 70879–83–3;
70955–07–6; 71011–10–4; 71060–57–6; 71243–46–4; 72066–65–0; 72108–90–8; 72484–69–6; 72854–13–8;
72905–87–4; 73018–31–2; 73049–34–0; 74432–13–6; 74499–34–6; 78330–19–5; 78330–20–8; 78330–21–9;
78330–23–1; 79771–03–2; 84133–50–6; 85422–93–1; 97043–91–9; 97953–22–5; 102782–43–4; 103331–86–
8; 103657–84–7; 103657–85–8; 103818–93–5; 103819–03–0; 106232–83–1; 111905–54–5; 116810–31–2;
116810–32–3; 116810–33–4; 120313–48–6; 120944–68–5; 121617–09–2; 126646–02–4; 126950–62–7;
127036–24–2; 139626–71–4; 152231–44–2; 154518–36–2; 157627–86–6; 157627–88–8; 157707–41–0;
157707–43–2; 159653–49–3; 160875–66–1; 160901–20–2; 160901–09–7; 160901–19–9; 161025–21–4;
161025–22–5; 166736–08–9; 169107–21–5; 172588–43–1; 176022–76–7; 196823–11–7; 287935–46–0;
288260–45–7; 303176–75–2; 954108–36–2; 2222805–23–2
*
*
*
*
*
[FR Doc. 2019–18362 Filed 8–26–19; 8:45 am]
178 (see also Unit I.C. of the
BILLING CODE 6560–50–P
SUPPLEMENTARY INFORMATION).
40 CFR Part 180
[EPA–HQ–OPP–2018–0088; FRL–9997–10]
Emamectin Benzoate; Pesticide
Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
tolerances for residues of emamectin
benzoate (referred to as emamectin in
this document) in or on multiple
commodities which are identified and
discussed later in this document.
Interregional Research Project No. 4 (IR–
4) and Syngenta Crop Protection, LLC
requested these tolerances under the
Federal Food, Drug, and Cosmetic Act
(FFDCA).
jspears on DSK3GMQ082PROD with RULES
SUMMARY:
This regulation is effective
August 27, 2019. Objections and
requests for hearings must be received
on or before October 28, 2019, and must
be filed in accordance with the
instructions provided in 40 CFR part
DATES:
A. Does this action apply to me?
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2018–0088, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
VerDate Sep<11>2014
17:38 Aug 26, 2019
Jkt 247001
FOR FURTHER INFORMATION CONTACT:
Michael Goodis, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; main telephone number:
(703) 305–7090; email address:
RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00038
Fmt 4700
Sfmt 4700
*
I. General Information
ADDRESSES:
ENVIRONMENTAL PROTECTION
AGENCY
*
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 Publishing Office’s eCFR site at https://www.ecfr.gov/cgi-bin/
text-idx?&c=ecfr&tpl=/ecfrbrowse/
Title40/40tab_02.tpl.
E:\FR\FM\27AUR1.SGM
27AUR1
Agencies
[Federal Register Volume 84, Number 166 (Tuesday, August 27, 2019)]
[Rules and Regulations]
[Pages 44712-44718]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-18362]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2019-0093; FRL-9996-95]
Oxirane, 2-methyl-, Polymer With Oxirane, Monoundecyl Ether,
Branched and Linear; Exemption From the Requirement of a Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes an exemption from the requirement
of a tolerance for residues of oxirane, 2-methyl-, polymer with
oxirane, monoundecyl ether, branched and linear (CAS Reg. No. 2222805-
23-2) when used as an inert ingredient in a pesticide chemical
formulation. Exponent, Inc. on behalf of Clariant Corporation submitted
a petition to EPA under the Federal Food, Drug, and Cosmetic Act
(FFDCA), requesting an amendment to an existing requirement of a
tolerance. This regulation eliminates the need to establish a maximum
permissible level for residues of oxirane, 2-methyl-, polymer with
oxirane, monoundecyl ether, branched and linear.
DATES: This regulation is effective August 27, 2019. Objections and
requests for hearings must be received on or before October 28, 2019,
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-2019-0093, is available at https://www.regulations.gov or at the Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the Environmental Protection Agency
Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334,
1301 Constitution Ave. NW, Washington, DC 20460-0001. The Public
Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805. Please review the visitor instructions and
additional information about the docket available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Michael Goodis, Registration Division
(7505P), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave. NW, Washington, DC 20460-0001; main telephone
number: (703) 305-7090; email address: [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).
[[Page 44713]]
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 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, 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-2019-0093 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 28, 2019. 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-2019-0093, 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. Petition for Exemption
In the Federal Register of August 5, 2009 (74 FR 38935) (FRL-8430-
1), EPA issued a final rule, announcing the establishment of a
tolerance exemption pursuant to a pesticide petition (PP 9E7534) by The
Joint Inerts Task Force, Cluster Support Team 1 (CST 1), c/o CropLife
America, 1156 15th Street NW, Suite 400, Washington, DC 20005. The
petition requested that 40 CFR 180.910, 180.930, 180.940(a) and 180.960
be amended by establishing an exemption from the requirement of a
tolerance for residues of a group of substances known as [alpha]-alkyl-
[omega]-hydroxypoly(oxypropylene) and/or poly (oxyethylene) polymers
where the alkyl chain contains a minimum of 6 carbons, herein referred
to in this document as AAA.
The current petition seeks to expand the exemptions for AAA by
adding additional CAS Reg. Nos. In the Federal Register of May 13, 2019
(84 FR 20843) (FRL-9991-91), EPA issued a document pursuant to FFDCA
section 408, 21 U.S.C. 346a, announcing the filing of a pesticide
petition (PP IN-11254) by Exponent Inc. on behalf of Clariant
Corporation, Suite 1100, 1150 Connecticut Avenue NW, Washington DC
20036. The petition requested that 40 CFR 180.910, 180.930, 180.940(a)
and 180.960 be amended by establishing an exemption from the
requirement of a tolerance for residues of oxirane, 2-methyl-, polymer
with oxirane, monoundecyl ether, branched and linear (CAS Reg. No.
2222805-23-2). That document referenced a summary of the petition
prepared by Exponent, the petitioner, 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 has
confirmed that the requested CAS Reg. No. is acceptable for
consideration under the currently approved descriptor. This
determination is based on the Agency's risk assessment which can be
found at https://www.regulations.gov in document ``Alkyl Alcohol
Alkoxylates (AAA-JITF CST 1 Inert Ingredient), Human Health Risk
Assessment to Support Proposed Exemption from the Requirement of a
Tolerance under 40 CFR 180.960 when used as an Inert Ingredient in
Pesticide Formulations'' in docket ID number EPA-HQ-OPP-2009-0145.
III. Inert Ingredient Definition
Inert ingredients are all ingredients that are not active
ingredients as defined in 40 CFR 153.125 and include, but are not
limited to, the following types of ingredients (except when they have a
pesticidal efficacy of their own): Solvents such as alcohols and
hydrocarbons; surfactants such as polyoxyethylene polymers and fatty
acids; carriers such as clay and diatomaceous earth; thickeners such as
carrageenan and modified cellulose; wetting, spreading, and dispersing
agents; propellants in aerosol dispensers; microencapsulating agents;
and emulsifiers. The term ``inert'' is not intended to imply
nontoxicity; the ingredient may or may not be chemically active.
Generally, EPA has exempted inert ingredients from the requirement of a
tolerance based on the low toxicity of the individual inert
ingredients.
IV. Aggregate Risk Assessment and Determination of Safety
Section 408(c)(2)(A)(i) of FFDCA allows EPA to establish an
exemption from the requirement for 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. . . .''
EPA establishes exemptions from the requirement of a tolerance only
in those cases where it can be clearly demonstrated that the risks from
aggregate exposure to pesticide chemical residues under reasonably
foreseeable circumstances will pose no appreciable risks to human
health. In order to determine the risks from aggregate exposure to
pesticide inert ingredients, the Agency considers the toxicity of the
inert in conjunction with possible exposure to residues of the inert
ingredient through food, drinking water, and through other exposures
that
[[Page 44714]]
occur as a result of pesticide use in residential settings. If EPA is
able to determine that a finite tolerance is not necessary to ensure
that there is a reasonable certainty that no harm will result from
aggregate exposure to the inert ingredient, an exemption from the
requirement of a tolerance may be established.
Consistent with FFDCA section 408(c)(2)(A), and the factors
specified in FFDCA section 408(c)(2)(B), 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 oxirane, 2-methyl-, polymer
with oxirane, monoundecyl ether, branched and linear including exposure
resulting from the exemption established by this action. EPA's
assessment of exposures and risks associated with oxirane, 2-methyl-,
polymer with oxirane, monoundecyl ether, branched and linear follows.
A. Toxicological Profile
EPA has evaluated the available toxicity data and considered their
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. Specific information on the studies received and the nature
of the adverse effects caused by AAA as well as the no-observed-
adverse-effect-level (NOAEL) and the lowest-observed-adverse-effect-
level (LOAEL) from the toxicity studies are discussed in the final rule
published in the Federal Register of August 5, 2009 (74 FR 38935) (FRL-
8430-1).
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 https://www.epa.gov/pesticides/factsheets/riskassess.htm.
A summary of the toxicological endpoints for AAA used for human
risk assessment is discussed in Unit IV of the final rule published in
the Federal Register of August 5, 2009 (74 FR 38938) (FRL-8430-1).
C. Exposure Assessment
1. Dietary exposure from food and feed uses. In evaluating dietary
exposure to AAA, EPA considered exposure under the proposed exemption
from the requirement of a tolerance. EPA assessed dietary exposures
from AAA in food as follows:
i. Acute exposure. No adverse effects attributable to a single
exposure of the AAAs was seen in the toxicity databases. Therefore,
acute dietary risk assessments for the AAAs are not necessary.
ii. Chronic exposure. In conducting the chronic dietary exposure
assessment, EPA used food consumption information from the U.S.
Department of Agriculture (USDA) 1994 -1996 and 1998 Nationwide
Continuing Surveys of Food Intake by Individuals (CSFII).
iii. Cancer. The Agency used a qualitative structure activity
relationship (SAR) database, DEREK11, to determine if there were
structural alerts suggestive of carcinogenicity. No structural alerts
for carcinogenicity were identified. The AAAs are not expected to be
carcinogenic. Therefore, a cancer dietary exposure assessment is not
necessary to assess cancer risk.
2. Dietary exposure from drinking water. The Agency used screening
level water exposure models in the dietary exposure analysis and risk
assessment for the AAAs in drinking water.
3. From non-dietary exposure. The term ``residential exposure'' is
used in this document to refer to nonoccupational, non-dietary exposure
(e.g., for lawn and garden pest control, indoor pest control,
termiticides, and flea and tick control on pets). The AAAs may be used
in inert ingredients in pesticide products that are registered for
specific uses that may result in both indoor and outdoor residential
exposures. A screening level residential exposure and risk assessment
was completed for products containing the AAAs as inert ingredients.
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.''
EPA has not found AAA to share a common mechanism of toxicity with
any other substances, and AAA does not appear to produce a toxic
metabolite produced by other substances. For the purposes of this
tolerance action, therefore, EPA has assumed that AAA does not have 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/pesticides/cumulative.
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. In the case of the lower
weight AAA surfactants, there was no evidence of increased
susceptibility to the offspring of rats following prenatal and
postnatal exposure in the reproductive/developmental screening studies
on several representative AAA surfactants. Decreased litter size and
increased post-implantation loss were observed in one OPPTS Harmonized
Guideline 870.3550 reproduction/developmental toxicity screening study
at 470 mg/kg/day where maternal/paternal toxicity was manifested as one
maternal death (GD
[[Page 44715]]
22), decreased body weight, bodyweight gain and food consumption and
clinical signs (ptosis and hypoactivity) and microscopic changes in the
testes (atrophy) and epididymides (increased intraluminal exfoliated
spermatogenic cells) and dilated seminiferous tubules at the same dose
(470 mg/kg/day). The maternal and offspring toxicity NOAEL was 168 mg/
kg/day. The offspring toxicity in the OPPTS Harmonized Test Guideline
870.3650 study was manifested in the presence of more severe maternal
toxicity (deaths), therefore, EPA concluded that there is no evidence
of increased susceptibility in this study. In addition, there was no
evidence of increased susceptibility in other submitted studies.
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 for the lower weight AAAs. (As discussed
earlier, given the low toxicological concerns with the high weight
AAAs, a safety factor analysis is unnecessary).
E. Aggregate Risks and Determination of Safety Determination of Safety
Section
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,
AAA is not expected to pose an acute risk.
2. Chronic risk. A chronic aggregate risk assessment takes into
account exposure estimates from chronic dietary consumption of food and
drinking water. Using the exposure assumptions discussed in this unit
for chronic exposure the chronic dietary exposure from food and water
to the AAAs is 11% of the cPAD for the U.S. population and 37% of the
cPAD for children 1 to 2 years old, the most highly exposed population
subgroup.
3. Short-term risk. Short-term aggregate exposure takes into
account short-term residential exposure plus chronic exposure to food
and water (considered to be a background exposure level).
AAAs are used as inert ingredients in pesticide products that are
currently registered for uses that could result in short-term
residential exposure and the Agency has determined that it is
appropriate to aggregate chronic exposure through food and water with
short-term residential exposures to the AAAs. EPA has concluded that
the combined short-term aggregated food, water, and residential
exposures result in aggregate MOEs of 110 for both adult males and
females. Adult residential exposure combines high end indoor inhalation
handler exposure with a high-end post application to pet exposures. EPA
has concluded the combined short-term aggregated food, water, and
residential exposures result in an aggregate MOE of 110 for children.
Children's residential exposure includes total combined pet exposures.
As the level of concern is for MOEs that are lower than 100, these MOEs
are not of concern.
4. Intermediate-term risk. Intermediate-term aggregate exposure
takes into account intermediate-term residential exposure plus chronic
exposure to food and water (considered to be a background exposure
level).
The AAAs are used as inert ingredients in pesticide products that
are currently registered for uses that could result in intermediate-
term residential exposure and the Agency has determined that it is
appropriate to aggregate chronic exposure through food and water with
intermediate-term residential exposures to the AAAs. EPA has concluded
that the combined intermediate-term aggregated food, water, and
residential exposures result in aggregate MOEs of 230 for both adult
males and females, respectively. Adult residential exposure includes
high-end post application dermal exposure from contact with treated
pets. EPA has concluded that the combined intermediate-term aggregated
food, water, and residential exposures result in an aggregate MOE of
110 for children. Children's residential exposure includes total
combined pet exposure. As the level of concern is for MOEs that are
lower than 100, these MOEs are not of concern.
5. Aggregate cancer risk for U.S. population. The Agency has not
identified any concerns for carcinogenicity relating to the AAAs.
6. 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 residues of the lower weight AAAs. For the high molecular
weight AAAs under 40 CFR 180.960. Since AAA conforms to the criteria
that identify a low-risk polymer, there are no concerns for risks
associated with any potential exposure scenarios that are reasonably
foreseeable. Therefore, 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 residues of the high
molecular weight AAAs.
V. Other Considerations
A. Analytical Enforcement Methodology
An analytical method is not required for enforcement purposes since
the Agency is establishing an exemption from the requirement of a
tolerance without any numerical limitation.
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 Nation 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 AAAs.
VI. Conclusions
Therefore, an exemption from the requirement of a tolerance is
established for residues of the lower molecular weight [alpha]-alkyl-
[omega]-hydroxypoly(oxypropylene) and/or poly (oxyethylene) polymers
where the alkyl chain contains a minimum of 6 carbons, including
oxirane, 2-methyl-, polymer with oxirane, monoundecyl ether, branched
and linear (CAS Reg. No. 2222805-23-2) when used as an inert ingredient
in pesticide formulations applied to pre- and post-harvest, applied to
livestock, and used in antimicrobial formulations under 40 CFR 180.910,
40 CFR 180.930, and 40 CFR 180.940(a). In addition, an
[[Page 44716]]
exemption from the requirement of a tolerance is established for
residues of the larger molecular weight compounds of a-alkyl-w-
hydroxypoly (oxypropylene) and/or poly (oxyethylene) polymers where the
alkyl chain contains a minimum of 6 carbons, including oxirane, 2-
methyl-, polymer with oxirane, monoundecyl ether, branched and linear
(CAS Reg. No. 2222805-23-2) under 40 CFR 180.960.
VII. 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).
VIII. 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: August 16, 2019.
Daniel Rosenblatt,
Acting Director, Registration Division, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. In Sec. 180.910, revise the inert ingredients ``[alpha]-Alkyl-
[omega]-hydroxypoly (oxypropylene) and/or poly (oxyethylene) polymers
where the alkyl chain contains a minimum of six carbons'' in the table
to read as follows:
Sec. 180.910 Inert ingredients used pre- and post-harvest; exemptions
from the requirement of a tolerance.
* * * * *
------------------------------------------------------------------------
Inert ingredients Limits Uses
------------------------------------------------------------------------
* * * * * * *
[alpha]-Alkyl-[omega]-hydroxypoly ........... Surfactants,
(oxypropylene) and/or poly (oxyethylene) related
polymers where the alkyl chain contains adjuvants of
a minimum of six carbons (CAS Reg. Nos.: surfactants
9002-92-0; 9004-95-9; 9004-98-2; 9005-00-
9; 9035-85-2; 9038-29-3; 9038-43-1; 9040-
05-5; 9043-30-5; 9087-53-0; 25190-05-0;
24938-91-8; 25231-21-4; 251553-55-6;
26183-52-8; 26468-86-0; 26636-39-5;
27252-75-1; 27306-79-2; 31726-34-8;
34398-01-1; 34398-05-5; 37251-67-5;
37311-00-5; 37311-01-6; 37311-02-7;
37311-04-9; 39587-22-9; 50861-66-0;
52232-09-4; 52292-17-8; 52609-19-5;
57679-21-7; 59112-62-8; 60828-78-6;
61702-78-1; 61723-78-2; 61725-89-1;
61791-13-7; 61791-20-6; 61791-28-4;
61804-34-0; 61827-42-7; 61827-84-7;
62648-50-4; 63303-01-5; 63658-45-7;
63793-60-2; 64366-70-7; 64415-24-3;
64415-25-4; 64425-86-1; 65104-72-5;
65150-81-4; 66455-14-9: 66455-15-0;
67254-71-1; 67763-08-0; 68002-96-0;
68002-97-1; 68131-39-5; 68131-40-8;
68154-96-1; 68154-97-2; 68154-98-3;
68155-01-1; 68213-23-0; 68213-24-1;
68238-81-3; 68238-82-4; 68409-58-5;
68409-59-6; 68439-30-5; 68439-45-2;
68439-46-3; 68439-48-5; 68439-49-6;
68439-50-9; 68439-51-0; 68439-53-2;
68439-54-3; 68458-88-8; 68526-94-3;
68526-95-4; 68551-12-2; 68551-13-3;
68551-14-4; 68603-20-3; 68603-25-8;
68920-66-1; 68920-69-4; 68937-66-6;
68951-67-7; 68954-94-9; 68987-81-5;
68991-48-0; 69011-36-5; 69013-18-9;
69013-19-0; 69227-20-9; 69227-21-0;
69227-22-1; 69364-63-2; 70750-27-5;
70879-83-3; 70955-07-6; 71011-10-4;
71060-57-6; 71243-46-4; 72066-65-0;
72108-90-8; 72484-69-6; 72854-13-8;
72905-87-4; 73018-31-2; 73049-34-0;
74432-13-6; 74499-34-6; 78330-19-5;
78330-20-8; 78330-21-9; 78330-23-1;
79771-03-2; 84133-50-6; 85422-93-1;
97043-91-9; 97953-22-5; 102782-43-4;
103331-86-8; 103657-84-7; 103657-85-8;
103818-93-5; 103819-03-0; 106232-83-1;
111905-54-5; 116810-31-2; 116810-32-3;
116810-33-4; 120313-48-6; 120944-68-5;
121617-09-2; 126646-02-4; 126950-62-7;
127036-24-2; 139626-71-4; 152231-44-2;
154518-36-2; 157627-86-6; 157627-88-8;
157707-41-0; 157707-43-2; 159653-49-3;
160875-66-1; 160901-20-2; 160901-09-7;
160901-19-9; 161025-21-4; 161025-22-5;
166736-08-9; 169107-21-5; 172588-43-1;
176022-76-7; 196823-11-7; 287935-46-0;
288260-45-7; 303176-75-2; 954108-36-2;
2222805-23-2).
* * * * * * *
------------------------------------------------------------------------
[[Page 44717]]
0
3. In Sec. 180.930, revise the inert ingredients ``[alpha]-Alkyl-
[omega]-hydroxypoly (oxypropylene) and/or poly (oxyethylene) polymers
where the alkyl chain contains a minimum of six carbons'' in the table
to read as follows:
Sec. 180.930 Inert ingredients applied to animals; exemptions from
the requirement of a tolerance.
* * * * *
------------------------------------------------------------------------
Inert ingredients Limits Uses
------------------------------------------------------------------------
* * * * * * *
[alpha]-Alkyl-[omega]-hydroxypoly ........... Surfactants,
(oxypropylene) and/or poly (oxyethylene) related
polymers where the alkyl chain contains adjuvants of
a minimum of six carbons (CAS Reg. Nos.: surfactants
9002-92-0; 9004-95-9; 9004-98-2; 9005-00-
9; 9035-85-2; 9038-29-3; 9038-43-1; 9040-
05-5; 9043-30-5; 9087-53-0; 25190-05-0;
24938-91-8; 25231-21-4; 251553-55-6;
26183-52-8; 26468-86-0; 26636-39-5;
27252-75-1; 27306-79-2; 31726-34-8;
34398-01-1; 34398-05-5; 37251-67-5;
37311-00-5; 37311-01-6; 37311-02-7;
37311-04-9; 39587-22-9; 50861-66-0;
52232-09-4; 52292-17-8; 52609-19-5;
57679-21-7; 59112-62-8; 60828-78-6;
61702-78-1; 61723-78-2; 61725-89-1;
61791-13-7; 61791-20-6; 61791-28-4;
61804-34-0; 61827-42-7; 61827-84-7;
62648-50-4; 63303-01-5; 63658-45-7;
63793-60-2; 64366-70-7; 64415-24-3;
64415-25-4; 64425-86-1; 65104-72-5;
65150-81-4; 66455-14-9: 66455-15-0;
67254-71-1; 67763-08-0; 68002-96-0;
68002-97-1; 68131-39-5; 68131-40-8;
68154-96-1; 68154-97-2; 68154-98-3;
68155-01-1; 68213-23-0; 68213-24-1;
68238-81-3; 68238-82-4; 68409-58-5;
68409-59-6; 68439-30-5; 68439-45-2;
68439-46-3; 68439-48-5; 68439-49-6;
68439-50-9; 68439-51-0; 68439-53-2;
68439-54-3; 68458-88-8; 68526-94-3;
68526-95-4; 68551-12-2; 68551-13-3;
68551-14-4; 68603-20-3; 68603-25-8;
68920-66-1; 68920-69-4; 68937-66-6;
68951-67-7; 68954-94-9; 68987-81-5;
68991-48-0; 69011-36-5; 69013-18-9;
69013-19-0; 69227-20-9; 69227-21-0;
69227-22-1; 69364-63-2; 70750-27-5;
70879-83-3; 70955-07-6; 71011-10-4;
71060-57-6; 71243-46-4; 72066-65-0;
72108-90-8; 72484-69-6; 72854-13-8;
72905-87-4; 73018-31-2; 73049-34-0;
74432-13-6; 74499-34-6; 78330-19-5;
78330-20-8; 78330-21-9; 78330-23-1;
79771-03-2; 84133-50-6; 85422-93-1;
97043-91-9; 97953-22-5; 102782-43-4;
103331-86-8; 103657-84-7; 103657-85-8;
103818-93-5; 103819-03-0; 106232-83-1;
111905-54-5; 116810-31-2; 116810-32-3;
116810-33-4; 120313-48-6; 120944-68-5;
121617-09-2; 126646-02-4; 126950-62-7;
127036-24-2; 139626-71-4; 152231-44-2;
154518-36-2; 157627-86-6; 157627-88-8;
157707-41-0; 157707-43-2; 159653-49-3;
160875-66-1; 160901-20-2; 160901-09-7;
160901-19-9; 161025-21-4; 161025-22-5;
166736-08-9; 169107-21-5; 172588-43-1;
176022-76-7; 196823-11-7; 287935-46-0;
288260-45-7; 303176-75-2; 954108-36-2;
2222805-23-2).
* * * * * * *
------------------------------------------------------------------------
0
4. In Sec. 180.940, revise the inert ingredients ``[alpha]-Alkyl-
[omega]-hydroxypoly (oxypropylene) and/or poly (oxyethylene) polymers
where the alkyl chain contains a minimum of six carbons'' in the table
in paragraph (a) to read as follows:
Sec. 180.940 Tolerance exemptions for active and inert ingredients
for use in antimicrobial formulations (Food-contact surface sanitizing
solutions).
* * * * *
(a) * * *
----------------------------------------------------------------------------------------------------------------
Pesticide chemical CAS Reg. No. Limits
----------------------------------------------------------------------------------------------------------------
* * * * * * **
[alpha]-Alkyl-[omega]-hydroxypoly 9002-92-0; 9004-95-9; 9004-98-2; 9005-00-9; 9035- None
(oxypropylene) and/or poly 85-2; 9038-29-3; 9038-43-1; 9040-05-5; 9043-30-
(oxyethylene) polymers where the 5; 9087-53-0; 25190-05-0; 24938-91-8; 25231-21-
alkyl chain contains a minimum of 4; 251553-55-6; 26183-52-8; 26468-86-0; 26636-
six carbons. 39-5; 27252-75-1; 27306-79-2; 31726-34-8; 34398-
01-1; 34398-05-5; 37251-67-5; 37311-00-5; 37311-
01-6; 37311-02-7; 37311-04-9; 39587-22-9; 50861-
66-0; 52232-09-4; 52292-17-8; 52609-19-5; 57679-
21-7; 59112-62-8; 60828-78-6; 61702-78-1; 61723-
78-2; 61725-89-1; 61791-13-7; 61791-20-6; 61791-
28-4; 61804-34-0; 61827-42-7; 61827-84-7; 62648-
50-4; 63303-01-5; 63658-45-7; 63793-60-2; 64366-
70-7; 64415-24-3; 64415-25-4; 64425-86-1; 65104-
72-5; 65150-81-4; 66455-14-9: 66455-15-0; 67254-
71-1; 67763-08-0; 68002-96-0; 68002-97-1; 68131-
39-5; 68131-40-8; 68154-96-1; 68154-97-2; 68154-
98-3; 68155-01-1; 68213-23-0; 68213-24-1; 68238-
81-3; 68238-82-4; 68409-58-5; 68409-59-6; 68439-
30-5; 68439-45-2; 68439-46-3; 68439-48-5; 68439-
49-6; 68439-50-9; 68439-51-0; 68439-53-2; 68439-
54-3; 68458-88-8; 68526-94-3; 68526-95-4; 68551-
12-2; 68551-13-3; 68551-14-4; 68603-20-3; 68603-
25-8; 68920-66-1; 68920-69-4; 68937-66-6; 68951-
67-7; 68954-94-9; 68987-81-5; 68991-48-0; 69011-
36-5; 69013-18-9; 69013-19-0; 69227-20-9; 69227-
21-0; 69227-22-1; 69364-63-2; 70750-27-5; 70879-
83-3; 70955-07-6; 71011-10-4; 71060-57-6; 71243-
46-4; 72066-65-0; 72108-90-8; 72484-69-6; 72854-
13-8; 72905-87-4; 73018-31-2; 73049-34-0; 74432-
13-6; 74499-34-6; 78330-19-5; 78330-20-8; 78330-
21-9; 78330-23-1; 79771-03-2; 84133-50-6; 85422-
93-1; 97043-91-9; 97953-22-5; 102782-43-4;
103331-86-8; 103657-84-7; 103657-85-8; 103818-
93-5; 103819-03-0; 106232-83-1; 111905-54-5;
116810-31-2; 116810-32-3; 116810-33-4; 120313-
48-6; 120944-68-5; 121617-09-2; 126646-02-4;
126950-62-7; 127036-24-2; 139626-71-4; 152231-
44-2; 154518-36-2; 157627-86-6; 157627-88-8;
157707-41-0; 157707-43-2; 159653-49-3; 160875-
66-1; 160901-20-2; 160901-09-7; 160901-19-9;
161025-21-4; 161025-22-5; 166736-08-9; 169107-
21-5; 172588-43-1; 176022-76-7; 196823-11-7;
287935-46-0; 288260-45-7; 303176-75-2; 954108-
36-2; 2222805-23-2.
* * * * * * *
----------------------------------------------------------------------------------------------------------------
[[Page 44718]]
* * * * *
0
5. In Sec. 180.960, revise the inert ingredients ``[alpha]-Alkyl-
[omega]-hydroxypoly (oxypropylene) and/or poly (oxyethylene) polymers
where the alkyl chain contains a minimum of six carbons and a minimum
number average molecular weight (in amu) 1,100'' in the table to read
as follows:
Sec. 180.960 Polymers; exemptions from the requirement of a
tolerance.
* * * * *
------------------------------------------------------------------------
Polymer CAS No.
------------------------------------------------------------------------
* * * * * * *
[alpha]-Alkyl-[omega]- 9002-92-0; 9004-95-9; 9004-98-2; 9005-00-
hydroxypoly (oxypropylene) 9; 9035-85-2; 9038-29-3; 9038-43-1; 9040-
and/or poly (oxyethylene) 05-5; 9043-30-5; 9087-53-0; 25190-05-0;
polymers where the alkyl 24938-91-8; 25231-21-4; 251553-55-6;
chain contains a minimum of 26183-52-8; 26468-86-0; 26636-39-5;
six carbons and a minimum 27252-75-1; 27306-79-2; 31726-34-8;
number average molecular 34398-01-1; 34398-05-5; 37251-67-5;
weight (in amu) 1,100. 37311-00-5; 37311-01-6; 37311-02-7;
37311-04-9; 39587-22-9; 50861-66-0;
52232-09-4; 52292-17-8; 52609-19-5;
57679-21-7; 59112-62-8; 60828-78-6;
61702-78-1; 61723-78-2; 61725-89-1;
61791-13-7; 61791-20-6; 61791-28-4;
61804-34-0; 61827-42-7; 61827-84-7;
62648-50-4; 63303-01-5; 63658-45-7;
63793-60-2; 64366-70-7; 64415-24-3;
64415-25-4; 64425-86-1; 65104-72-5;
65150-81-4; 66455-14-9: 66455-15-0;
67254-71-1; 67763-08-0; 68002-96-0;
68002-97-1; 68131-39-5; 68131-40-8;
68154-96-1; 68154-97-2; 68154-98-3;
68155-01-1; 68213-23-0; 68213-24-1;
68238-81-3; 68238-82-4; 68409-58-5;
68409-59-6; 68439-30-5; 68439-45-2;
68439-46-3; 68439-48-5; 68439-49-6;
68439-50-9; 68439-51-0; 68439-53-2;
68439-54-3; 68458-88-8; 68526-94-3;
68526-95-4; 68551-12-2; 68551-13-3;
68551-14-4; 68603-20-3; 68603-25-8;
68920-66-1; 68920-69-4; 68937-66-6;
68951-67-7; 68954-94-9; 68987-81-5;
68991-48-0; 69011-36-5; 69013-18-9;
69013-19-0; 69227-20-9; 69227-21-0;
69227-22-1; 69364-63-2; 70750-27-5;
70879-83-3; 70955-07-6; 71011-10-4;
71060-57-6; 71243-46-4; 72066-65-0;
72108-90-8; 72484-69-6; 72854-13-8;
72905-87-4; 73018-31-2; 73049-34-0;
74432-13-6; 74499-34-6; 78330-19-5;
78330-20-8; 78330-21-9; 78330-23-1;
79771-03-2; 84133-50-6; 85422-93-1;
97043-91-9; 97953-22-5; 102782-43-4;
103331-86-8; 103657-84-7; 103657-85-8;
103818-93-5; 103819-03-0; 106232-83-1;
111905-54-5; 116810-31-2; 116810-32-3;
116810-33-4; 120313-48-6; 120944-68-5;
121617-09-2; 126646-02-4; 126950-62-7;
127036-24-2; 139626-71-4; 152231-44-2;
154518-36-2; 157627-86-6; 157627-88-8;
157707-41-0; 157707-43-2; 159653-49-3;
160875-66-1; 160901-20-2; 160901-09-7;
160901-19-9; 161025-21-4; 161025-22-5;
166736-08-9; 169107-21-5; 172588-43-1;
176022-76-7; 196823-11-7; 287935-46-0;
288260-45-7; 303176-75-2; 954108-36-2;
2222805-23-2
* * * * * * *
------------------------------------------------------------------------
[FR Doc. 2019-18362 Filed 8-26-19; 8:45 am]
BILLING CODE 6560-50-P