Tall Oil Fatty Acids; Exemption From the Requirement of a Tolerance, 46926-46929 [2017-21787]
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46926
Federal Register / Vol. 82, No. 194 / Tuesday, October 10, 2017 / Rules and Regulations
NEGATIVE DECLARATIONS FOR THE 2008 OZONE NAAQS
CTG source category
CTG reference document
Can Coating ....................................
Control of Volatile Organic Emissions from Existing Stationary Sources—Volume II: Surface Coating of
Cans, Coils, Paper, Fabrics, Automobiles, and Light-Duty Trucks (EPA–450/2–77–008, 05/1977).
Control Techniques Guidelines for Miscellaneous Metal and Plastic Parts Coatings (EPA–453/R–08–003,
09/2008).
Control of Volatile Organic Emissions from Existing Stationary Sources—Volume VII: Factory Surface
Coating of Flat Wood Paneling (EPA–450/2–78–032, 06/1978).
Control of Volatile Organic Emissions from Existing Stationary Sources—Volume III: Surface Coating of
Metal Furniture (EPA–450/2–77–032, 12/1977).
Control Techniques Guidelines for Miscellaneous Metal and Plastic Parts Coatings (EPA–453/R–08–003,
09/2008).
Control of Hydrocarbons from Tank Truck Gasoline Loading Terminals (EPA–450/2–77–026, 10/1977).
Drum Coating ..................................
Flat Wood Paneling Coating ...........
Metal Furniture Coating ..................
Pleasure Craft Coating ...................
Tank Truck Gasoline Loading Terminals.
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■
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conditional approval is treated as a
disapproval.
*
4. Revise § 52.248 to read as follows:
[FR Doc. 2017–21375 Filed 10–6–17; 8:45 am]
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§ 52.248 Identification of plan—conditional
approval.
(a) The EPA is conditionally
approving a California State
Implementation Plan (SIP) revision
submitted on November 13, 2015
updating the motor vehicle emissions
budgets for nitrogen oxides (NOX) and
coarse particulate matter (PM10) for the
1987 24-hour PM10 standard for the San
Joaquin Valley PM10 maintenance area.
The conditional approval is based on a
commitment from the State to submit a
SIP revision that demonstrates full
implementation of the contingency
provisions of the 2007 PM10
Maintenance Plan and Request for
Redesignation (September 20, 2007). If
the State fails to meet its commitment
by June 1, 2017, the approval is treated
as a disapproval.
(b) The EPA is conditionally
approving portions of the California SIP
revisions submitted on January 31, 2007
and October 23, 2015, demonstrating
control measures in the Antelope Valley
portion of the Los Angeles-San
Bernardino Counties (West Mojave
Desert) nonattainment area implement
RACT for the 1997 and 2008 ozone
standards. The conditional approval is
based on a commitment from the state
to submit new or revised rules that will
correct deficiencies in the following
rules for the Antelope Valley Air
Quality Management District:
(1) Rule 462, Organic Liquid Loading;
(2) Rule 1110.2, Emissions from
Stationary, Non-road & Portable
Internal Combustion Engines;
(3) Rule 1151, Motor Vehicle and
Mobile Equipment Coating Operations;
and
(4) Rule 1171, Solvent Cleaning
Operations. If the State fails to meet its
commitment by November 9, 2018, the
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14:55 Oct 06, 2017
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BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2017–0012; FRL–9965–58]
Tall Oil Fatty Acids; Exemption From
the Requirement of a Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
exemptions from the requirement of a
tolerance for residues of tall oil fatty
acids (CAS Reg. No. 61790–12–3) when
used as inert ingredients (solvent/
carrier) in the following circumstances:
In pesticide formulations applied to
growing crops and raw agricultural
commodities after harvest; in pesticides
applied in/on animals, and in
antimicrobial formulations for food
contact surfaces. Spring Trading
Company on behalf of Ingevity
Corporation submitted a petition to EPA
under the Federal Food, Drug, and
Cosmetic Act (FFDCA), requesting
establishment of these exemptions from
the requirement of a tolerance. This
regulation eliminates the need to
establish maximum permissible levels
for residues of tall oil fatty acids that are
consistent with the conditions of these
exemptions.
DATES: This regulation is effective
October 10, 2017. Objections and
requests for hearings must be received
on or before December 11, 2017, and
must be filed in accordance with the
instructions provided in 40 CFR part
178 (see also Unit I.C. of the
SUPPLEMENTARY INFORMATION).
SUMMARY:
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The docket for this action,
identified by docket identification (ID)
number: EPA–HQ–OPP–2017–0012, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Michael L. Goodis, Registration Division
(7505P), 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:
ADDRESSES:
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).
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Federal Register / Vol. 82, No. 194 / Tuesday, October 10, 2017 / Rules and Regulations
II. Petition for Exemption
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 Printing
Office’s e-CFR site at https://
www.ecfr.gov/cgi-bin/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl.
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C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2017–0012 in the subject line on
the first page of your submission. All
objections and requests for a hearing
must be in writing, and must be
received by the Hearing Clerk on or
before December 11, 2017. Addresses for
mail and hand delivery of objections
and hearing requests are provided in 40
CFR 178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
disclosed publicly by EPA without prior
notice. Submit the non-CBI copy of your
objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2017–0012, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be CBI or
other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW., Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
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In the Federal Register of April 10,
2017 (82 FR 17175) (FRL–9959–61),
EPA issued a document pursuant to
FFDCA section 408, 21 U.S.C. 346a,
announcing the filing of pesticide
petition (IN–11002) by Spring Trading
Company (203 Dogwood Trail,
Magnolia, TX 77354) on behalf of
Ingevity Corporation (5255 Virginia
Avenue, North Charleston, SC 29406).
This petition requested that 40 CFR
180.910, 40 CFR 180.930, and 40 CFR
180.940(a) be amended by establishing
exemptions from the requirement of a
tolerance for residues of tall oil fatty
acids (CAS Reg. No. 61790–12–3) when
used as an inert ingredient (solvent/
carrier) in pesticide formulations
applied to growing crops and to raw
agricultural commodities after harvest,
in pesticides applied in/on animals, or
in antimicrobial formulations for food
contact surfaces. That document
referenced the summary of the petition
prepared by Spring Trading Company
on behalf of Ingevity Corporation, the
petitioner, which are available in the
docket, https://www.regulations.gov.
There were no comments received in
response to the notice of filing.
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(c)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
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46927
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
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 tall oil fatty acids
including exposure resulting from the
exemption established by this action.
EPA’s assessment of exposures and risks
associated with tall oil fatty acids
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
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Federal Register / Vol. 82, No. 194 / Tuesday, October 10, 2017 / Rules and Regulations
the U.S. population, including infants
and children.
from tall oil fatty acids in food as
follows:
Dietary exposure (food and drinking
water) to tall oil fatty acids can occur
following ingestion of foods with
residues from treated crops, animals or
food contact surfaces. Use on food crops
may result in residues in drinking
water.
2. From non-dietary exposure. The
term ‘‘residential exposure’’ is used in
this document to refer to nonoccupational, non-dietary exposure
(e.g., textiles (clothing and diapers),
carpets, swimming pools, and hard
surface disinfection on walls, floors,
tables).
Tall oil fatty acids may be used in
pesticide products and non-pesticide
products that may be used in and
around the home. Based on the
discussion above, a quantitative
residential exposure assessment for tall
oil fatty acids was not conducted.
3. 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.’’
Based on the available data, tall oil
fatty acids do not have a toxic
mechanism; therefore, section
408(b)(2)(D)(v) does not apply.
D. Safety Factor for Infants and
Children
VI. Conclusions
Therefore, exemptions from the
requirement of a tolerance are
established under for residues of tall oil
fatty acids (CAS Reg. No. 61790–12–3)
when used as an inert ingredient
(solvent/carrier) in pesticide
formulations as follows: For application
to growing crops and raw agricultural
commodities after harvest under 40 CFR
180.910; for application to animals
under 40 CFR 180.930; and for use in
antimicrobial pesticide formulations
applied to for food contact surfaces in
public eating places, dairy-processing
equipment, and food-processing
equipment and utensils under 40 CFR
180.940(a).
B. Toxicological Points of Departure/
Levels of Concern
The available toxicity studies indicate
that tall oil fatty acids have a very low
overall toxicity. The NOAELs in a 90day oral and a reproduction toxicity
studies were ≥5,000 mg/kg/day; well
above the limit dose of 1,000 mg/kg/day.
Since no signs of toxicity were
observed, even at doses above the limit
dose, an endpoint of concern for risk
assessment purposes was not identified.
Therefore, a qualitative risk assessment
was conducted for acute and chronic
dietary exposures and short and
intermediate dermal and inhalation
exposures.
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by tall oil fatty acids as well as the noobserved-adverse-effect-level (NOAEL)
and the lowest-observed-adverse-effectlevel (LOAEL) from the toxicity studies
are discussed in this unit.
The acute oral toxicity is low in rats
for tall oil fatty acids; the lethal dose
(LD50) is >10,000 milligrams/kilogram
(mg/kg). Tall oil fatty acids are not a
dermal sensitizer in the guinea pig
maximization test. Acute dermal
toxicity (study available with oleic acid)
was not observed in guinea pigs. Skin
and eye irritation and inhalation studies
are not available.
Tall oil fatty acids do not exhibit
toxicity when administered via the diet
to rats at 2,500 mg/kg/day for 90 days.
A two-generation reproduction
toxicity study in rats was available for
tall oil fatty acids. Fetal susceptibility
was not observed. Neither maternal nor
developmental adverse effects were
observed following oral administration
of tall oil fatty acids at doses as high as
5,000 mg/kg/day.
Carcinogenicity studies with tall oil
fatty acids are not available; however,
there is no toxicological endpoint of
concern up to 5,000 mg/kg/day nor is
there a potential for mutagenicity.
Therefore, tall oil fatty acids are not
expected to be carcinogenic.
Mutagenicity studies, the Ames test
and mammalian gene mutations, are
negative for tall fatty acids. Therefore,
tall oil fatty acids are not mutagenic.
Neurotoxicity and immunotoxicity
studies are not available for review;
however, evidence of neurotoxicity and
immunotoxicity is not observed in the
submitted studies.
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.
As part of its qualitative assessment,
the Agency did not use safety factors for
assessing risk, and no additional safety
factor is needed for assessing risk to
infants and children. Based on an
assessment of tall oil fatty acids, EPA
has concluded that there are no
toxicological endpoints of concern for
VII. Statutory and Executive Order
Reviews
This action establishes exemptions
from the requirement of a tolerance
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) 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
C. Exposure Assessment
1. Dietary exposure from food and
feed uses. In evaluating dietary
exposure to tall oil fatty acids, EPA
considered exposure under the
proposed exemption from the
requirement of a tolerance. EPA
qualitatively assessed dietary exposures
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E. Aggregate Risks and Determination of
Safety
Because no toxicological endpoints of
concern were identified, EPA concludes
that aggregate exposure to residues of
tall oil fatty acids will not pose a risk
to the U.S. population, including infants
and children, and that there is a
reasonable certainty that no harm will
result to the general population, or to
infants and children from aggregate
exposure to tall oil fatty acids residues.
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.
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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 exemptions 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,
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Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: September 5, 2017.
Michael Goodis,
Director, Registration Division, Office of
Pesticide Programs.
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46929
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[FR Doc. 2017–21787 Filed 10–6–17; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
Therefore, 40 CFR chapter I is
amended as follows:
40 CFR Part 180
PART 180—[AMENDED]
Tolfenpyrad; Pesticide Tolerances for
Emergency Exemptions
[EPA–HQ–OPP–2017–0309; FRL–9967–72]
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, add alphabetically the
inert ingredient to the table to read as
follows:
■
§ 180.910 Inert ingredients used pre- and
post-harvest; exemptions from the
requirement of a tolerance.
*
*
*
*
Inert ingredients
*
*
Tall oil fatty acids
(CAS Reg. No.
61790–12–3).
*
*
Limits
*
............
*
*
Uses
*
*
Solvent/carrier.
*
*
3. In § 180.930, add alphabetically the
inert ingredient to the table to read as
follows:
■
§ 180.930 Inert ingredients applied to
animals; exemptions from the requirement
of a tolerance.
*
*
*
*
Inert ingredients
*
*
Tall oil fatty acids
(CAS Reg. No.
61790–12–3).
*
*
Limits
*
............
*
*
Uses
*
*
Solvent/carrier.
*
*
4. In § 180.940(a), add alphabetically
the inert ingredient to the table to read
as follows:
■
§ 180.940(a) Tolerance exemptions for
active and inert ingredients for use in
antimicrobial formulations (Food contact
surface sanitizing solutions).
*
*
*
(a) * * *
*
Inert ingredients
*
*
Tall oil fatty acid
(CAS Reg. No.
61790–12–3).
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*
Limits
*
............
*
Fmt 4700
*
Uses
*
*
Solvent/carrier.
*
Sfmt 4700
*
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
time-limited tolerances for residues of
tolfenpyrad in or on dry bulb onion and
watermelon. This action is in response
to EPA’s granting of emergency
exemptions under the Federal
Insecticide, Fungicide, and Rodenticide
Act (FIFRA) authorizing use of the
pesticide on dry bulb onion and
watermelon. This regulation establishes
maximum permissible levels for
residues of tolfenpyrad in or on these
commodities. The time-limited
tolerances expire on December 31, 2020.
DATES: This regulation is effective
October 10, 2017. Objections and
requests for hearings must be received
on or before December 11, 2017, and
must be filed in accordance with the
instructions provided in 40 CFR part
178 (see also Unit I.C. of the
SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2017–0309, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Michael L. Goodis, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
DC 20460–0001; main telephone
number: (703) 305–7090; email address:
RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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Agencies
[Federal Register Volume 82, Number 194 (Tuesday, October 10, 2017)]
[Rules and Regulations]
[Pages 46926-46929]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-21787]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2017-0012; FRL-9965-58]
Tall Oil Fatty Acids; Exemption From the Requirement of a
Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes exemptions from the requirement of
a tolerance for residues of tall oil fatty acids (CAS Reg. No. 61790-
12-3) when used as inert ingredients (solvent/carrier) in the following
circumstances: In pesticide formulations applied to growing crops and
raw agricultural commodities after harvest; in pesticides applied in/on
animals, and in antimicrobial formulations for food contact surfaces.
Spring Trading Company on behalf of Ingevity Corporation submitted a
petition to EPA under the Federal Food, Drug, and Cosmetic Act (FFDCA),
requesting establishment of these exemptions from the requirement of a
tolerance. This regulation eliminates the need to establish maximum
permissible levels for residues of tall oil fatty acids that are
consistent with the conditions of these exemptions.
DATES: This regulation is effective October 10, 2017. Objections and
requests for hearings must be received on or before December 11, 2017,
and must be filed in accordance with the instructions provided in 40
CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number: EPA-HQ-OPP-2017-0012, is available at
https://www.regulations.gov or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket) in the Environmental Protection
Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg.,
Rm. 3334, 1301 Constitution Ave. NW., Washington, DC 20460-0001. The
Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805. Please review the visitor instructions and
additional information about the docket available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Michael L. Goodis, Registration
Division (7505P), Registration Division (7505P), Office of Pesticide
Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460-0001; main telephone number: (703) 305-7090; email
address: RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
[[Page 46927]]
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 Printing Office's e-CFR site at https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, any person may file an
objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2017-0012 in the subject line on the first
page of your submission. All objections and requests for a hearing must
be in writing, and must be received by the Hearing Clerk on or before
December 11, 2017. Addresses for mail and hand delivery of objections
and hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be disclosed publicly by EPA without
prior notice. Submit the non-CBI copy of your objection or hearing
request, identified by docket ID number EPA-HQ-OPP-2017-0012, 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 April 10, 2017 (82 FR 17175) (FRL-9959-
61), EPA issued a document pursuant to FFDCA section 408, 21 U.S.C.
346a, announcing the filing of pesticide petition (IN-11002) by Spring
Trading Company (203 Dogwood Trail, Magnolia, TX 77354) on behalf of
Ingevity Corporation (5255 Virginia Avenue, North Charleston, SC
29406). This petition requested that 40 CFR 180.910, 40 CFR 180.930,
and 40 CFR 180.940(a) be amended by establishing exemptions from the
requirement of a tolerance for residues of tall oil fatty acids (CAS
Reg. No. 61790-12-3) when used as an inert ingredient (solvent/carrier)
in pesticide formulations applied to growing crops and to raw
agricultural commodities after harvest, in pesticides applied in/on
animals, or in antimicrobial formulations for food contact surfaces.
That document referenced the summary of the petition prepared by Spring
Trading Company on behalf of Ingevity Corporation, the petitioner,
which are available in the docket, https://www.regulations.gov. There
were no comments received in response to the notice of filing.
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(c)(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 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 tall oil fatty acids including
exposure resulting from the exemption established by this action. EPA's
assessment of exposures and risks associated with tall oil fatty acids
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
[[Page 46928]]
by tall oil fatty acids 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 this unit.
The acute oral toxicity is low in rats for tall oil fatty acids;
the lethal dose (LD50) is >10,000 milligrams/kilogram (mg/
kg). Tall oil fatty acids are not a dermal sensitizer in the guinea pig
maximization test. Acute dermal toxicity (study available with oleic
acid) was not observed in guinea pigs. Skin and eye irritation and
inhalation studies are not available.
Tall oil fatty acids do not exhibit toxicity when administered via
the diet to rats at 2,500 mg/kg/day for 90 days.
A two-generation reproduction toxicity study in rats was available
for tall oil fatty acids. Fetal susceptibility was not observed.
Neither maternal nor developmental adverse effects were observed
following oral administration of tall oil fatty acids at doses as high
as 5,000 mg/kg/day.
Carcinogenicity studies with tall oil fatty acids are not
available; however, there is no toxicological endpoint of concern up to
5,000 mg/kg/day nor is there a potential for mutagenicity. Therefore,
tall oil fatty acids are not expected to be carcinogenic.
Mutagenicity studies, the Ames test and mammalian gene mutations,
are negative for tall fatty acids. Therefore, tall oil fatty acids are
not mutagenic.
Neurotoxicity and immunotoxicity studies are not available for
review; however, evidence of neurotoxicity and immunotoxicity is not
observed in the submitted studies.
B. Toxicological Points of Departure/Levels of Concern
The available toxicity studies indicate that tall oil fatty acids
have a very low overall toxicity. The NOAELs in a 90-day oral and a
reproduction toxicity studies were =5,000 mg/kg/day; well
above the limit dose of 1,000 mg/kg/day. Since no signs of toxicity
were observed, even at doses above the limit dose, an endpoint of
concern for risk assessment purposes was not identified. Therefore, a
qualitative risk assessment was conducted for acute and chronic dietary
exposures and short and intermediate dermal and inhalation exposures.
C. Exposure Assessment
1. Dietary exposure from food and feed uses. In evaluating dietary
exposure to tall oil fatty acids, EPA considered exposure under the
proposed exemption from the requirement of a tolerance. EPA
qualitatively assessed dietary exposures from tall oil fatty acids in
food as follows:
Dietary exposure (food and drinking water) to tall oil fatty acids
can occur following ingestion of foods with residues from treated
crops, animals or food contact surfaces. Use on food crops may result
in residues in drinking water.
2. From non-dietary exposure. The term ``residential exposure'' is
used in this document to refer to non-occupational, non-dietary
exposure (e.g., textiles (clothing and diapers), carpets, swimming
pools, and hard surface disinfection on walls, floors, tables).
Tall oil fatty acids may be used in pesticide products and non-
pesticide products that may be used in and around the home. Based on
the discussion above, a quantitative residential exposure assessment
for tall oil fatty acids was not conducted.
3. 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.''
Based on the available data, tall oil fatty acids do not have a
toxic mechanism; therefore, section 408(b)(2)(D)(v) does not apply.
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.
As part of its qualitative assessment, the Agency did not use
safety factors for assessing risk, and no additional safety factor is
needed for assessing risk to infants and children. Based on an
assessment of tall oil fatty acids, EPA has concluded that there are no
toxicological endpoints of concern for the U.S. population, including
infants and children.
E. Aggregate Risks and Determination of Safety
Because no toxicological endpoints of concern were identified, EPA
concludes that aggregate exposure to residues of tall oil fatty acids
will not pose a risk to the U.S. population, including infants and
children, and that there is a reasonable certainty that no harm will
result to the general population, or to infants and children from
aggregate exposure to tall oil fatty acids residues.
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.
VI. Conclusions
Therefore, exemptions from the requirement of a tolerance are
established under for residues of tall oil fatty acids (CAS Reg. No.
61790-12-3) when used as an inert ingredient (solvent/carrier) in
pesticide formulations as follows: For application to growing crops and
raw agricultural commodities after harvest under 40 CFR 180.910; for
application to animals under 40 CFR 180.930; and for use in
antimicrobial pesticide formulations applied to for food contact
surfaces in public eating places, dairy-processing equipment, and food-
processing equipment and utensils under 40 CFR 180.940(a).
VII. Statutory and Executive Order Reviews
This action establishes exemptions from the requirement of a
tolerance under FFDCA section 408(d) in response to a petition
submitted to the Agency. The Office of Management and Budget (OMB) has
exempted these types of actions from review under Executive Order
12866, entitled ``Regulatory Planning and Review'' (58 FR 51735,
October 4, 1993). Because this action has been exempted from review
under Executive Order 12866, this action is not subject to Executive
Order 13211, entitled ``Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use'' (66 FR
28355, May 22, 2001) 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
[[Page 46929]]
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 exemptions 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: September 5, 2017.
Michael Goodis,
Director, Registration Division, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
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1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
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2. In Sec. 180.910, add alphabetically the inert ingredient to the
table to read as follows:
Sec. 180.910 Inert ingredients used pre- and post-harvest;
exemptions from the requirement of a tolerance.
* * * * *
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Inert ingredients Limits Uses
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* * * * *
Tall oil fatty acids (CAS Reg. No. ....... Solvent/carrier.
61790-12-3).
* * * * *
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3. In Sec. 180.930, add alphabetically the inert ingredient to the
table to read as follows:
Sec. 180.930 Inert ingredients applied to animals; exemptions from
the requirement of a tolerance.
* * * * *
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Inert ingredients Limits Uses
------------------------------------------------------------------------
* * * * *
Tall oil fatty acids (CAS Reg. No. ....... Solvent/carrier.
61790-12-3).
* * * * *
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4. In Sec. 180.940(a), add alphabetically the inert ingredient to the
table to read as follows:
Sec. 180.940(a) Tolerance exemptions for active and inert ingredients
for use in antimicrobial formulations (Food contact surface sanitizing
solutions).
* * * * *
(a) * * *
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Inert ingredients Limits Uses
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* * * * *
Tall oil fatty acid (CAS Reg. No. ....... Solvent/carrier.
61790-12-3).
* * * * *
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* * * * *
[FR Doc. 2017-21787 Filed 10-6-17; 8:45 am]
BILLING CODE 6560-50-P