Ammonium Salts of Fatty Acids (C8, 14082-14086 [2010-6495]
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Federal Register / Vol. 75, No. 56 / Wednesday, March 24, 2010 / Rules and Regulations
TABLE A–4 OF SUBPART A—SOURCE CATEGORY LIST FOR § 98.2(a)(2)—Continued
Lead production (subpart R).
Pulp and paper manufacturing (subpart AA).
Zinc production (subpart GG).
Additional Source Categories 1 Applicable in 2011 and Future Years
(Reserved)
1
Source categories are defined in each applicable subpart.
TABLE A–5 OF SUBPART A—SUPPLIER CATEGORY LIST FOR § 98.2(a)(4)
Supplier Categories 1 Applicable in 2010 and Future Years
Coal-to-liquids suppliers (subpart LL):
(A) All producers of coal-to-liquid products.
(B) Importers of an annual quantity of coal-to-liquid products that is equivalent to 25,000 metric tons CO2e or more.
(C) Exports of an annual quantity of coal-to-liquid products that is equivalent to 25,000 metric tons CO2e or more.
Petroleum product suppliers (subpart MM):
(A) All petroleum refineries that distill crude oil.
(B) Importers of an annual quantity of petroleum products that is equivalent to 25,000 metric tons CO2e or more.
(C) Exporters of an annual quantity of petroleum products that is equivalent to 25,000 metric tons CO2e or more.
Natural gas and natural gas liquids suppliers (subpart NN):
(A) All fractionators.
(B) All local natural gas distribution companies.
Industrial greenhouse gas suppliers (subpart OO):
(A) All producers of industrial greenhouse gases.
(B) Importers of industrial greenhouse gases with annual bulk imports of N2O, fluorinated GHG, and CO2 that in combination are equivalent
to 25,000 metric tons CO2e or more.
(C) Exporters of industrial greenhouse gases with annual bulk exports of N2O, fluorinated GHG, and CO2 that in combination are equivalent
to 25,000 metric tons CO2e or more.
Carbon dioxide suppliers (subpart PP):
(A) All producers of CO2.
(B) Importers of CO2 with annual bulk imports of N2O, fluorinated GHG, and CO2 that in combination are equivalent to 25,000 metric tons
CO2e or more.
(C) Exporters of CO2 with annual bulk exports of N2O, fluorinated GHG, and CO2 that in combination are equivalent to 25,000 metric tons
CO2e or more.
Additional Supplier Categories Applicable 1 in 2011 and Future Years
(Reserved)
1
Suppliers are defined in each applicable subpart.
[FR Doc. C1–2010–5695 Filed 3–23–10; 8:45 am]
BILLING CODE 1505–01–D
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2008–0652; FRL–8809–6]
Ammonium Salts of Fatty Acids (C8-C18
Saturated); Exemption from the
Requirement of a Tolerance
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AGENCY: Environmental Protection
Agency (EPA).
ACTION: Final rule.
This regulation establishes an
exemption from the requirement of a
tolerance for residues of ammonium
salts of fatty acids (C8-C18 saturated)
applied pre- and post-harvest on all raw
agricultural commodities when applied/
used as a surfactant. Falcon Lab, LLC.
submitted a petition to EPA under the
Federal Food, Drug, and Cosmetic Act
SUMMARY:
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(FFDCA), requesting an exemption from
the requirement of a tolerance. This
regulation eliminates the need to
establish a maximum permissible level
for residues of ammonium salts of fatty
acids (C8-C18 saturated).
DATES: This regulation is effective
March 24, 2010. Objections and requests
for hearings must be received on or
before May 24, 2010, 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: EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPP–2008–0652. All documents in the
docket are listed in the docket index
available at https://www.regulations.gov.
Although listed in the index, some
information is not publicly available,
e.g., Confidential Business Information
(CBI) or other information whose
disclosure is restricted by statute.
Certain other material, such as
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copyrighted material, is not placed on
the Internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available in the electronic docket at
https://www.regulations.gov, or, if only
available in hard copy, at the OPP
Regulatory Public Docket in Rm. S–
4400, One Potomac Yard (South Bldg.),
2777 S. Crystal Dr., Arlington, VA. The
Docket Facility is open from 8:30 a.m.
to 4 p.m., Monday through Friday,
excluding legal holidays. The Docket
Facility telephone number is (703) 305–
5805.
FOR FURTHER INFORMATION CONTACT:
Deirdre Sunderland, Registration
Division (7505P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (703) 603–0851; e-mail address:
sunderland.deirdre@epa.gov.
SUPPLEMENTARY INFORMATION:
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Federal Register / Vol. 75, No. 56 / Wednesday, March 24, 2010 / Rules and Regulations
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. Potentially
affected entities may include, but are
not limited to:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
assist you and others in determining
whether this action might apply to
certain entities. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
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B. How Can I Access Electronic Copies
of This Document?
You may access a frequently updated
electronic version of 40 CFR part 180
through the Government Printing
Office’s e-CFR cite at https://
www.gpoaccess.gov/ecfr.
C. Can I File an Objection or Hearing
Request?
Under section 408(g) of FFDCA, 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. The EPA procedural
regulations which govern the
submission of objections and requests
for hearings appear in 40 CFR part 178.
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–2008–0652 in the subject line on
the first page of your submission. All
requests must be in writing, and must be
mailed or delivered to the Hearing Clerk
on or before May 24, 2010.
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 that does not
contain any CBI for inclusion in the
public docket that is described in
ADDRESSES. Information not marked
confidential pursuant to 40 CFR part 2
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may be disclosed publicly by EPA
without prior notice. Submit your
copies, identified by docket ID number
EPA–HQ–OPP–2008–0652, by one of
the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
instructions for submitting comments.
• Mail: Office of Pesticide Programs
(OPP) Regulatory Public Docket (7502P),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001.
• Delivery: OPP Regulatory Public
Docket (7502P), Environmental
Protection Agency, Rm. S–4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. Deliveries
are only accepted during the Docket
Facility’s normal hours of operation
(8:30 a.m. to 4 p.m., Monday through
Friday, excluding legal holidays).
Special arrangements should be made
for deliveries of boxed information. The
Docket Facility telephone number is
(703) 305–5805.
II. Background and Statutory Findings
In the Federal Register of September
5, 2008 (73 FR 51817) (FRL–8380–4),
EPA issued a notice pursuant to section
408 of FFDCA, 21 U.S.C. 346a, as
amended by the Food Quality Protection
ACT (FQPA) (Public Law 104–170),
announcing the filing of a pesticide
petition (PP 8E7402) by Falcon Lab,
LLC, 1103 Norbee Drive, Wilmington,
DE 19803. The petition requested that
40 CFR 180.910 be amended by
establishing an exemption from the
requirement of a tolerance for residues
of ammonium salts of fatty acids (C8-C18
saturated) when used as an inert
ingredient in pesticide formulations
applied pre- and post-harvest. A request
for a tolerance exemption under 40 CFR
180.950 was withdrawn by the
company. That notice included a
summary of the petition prepared by the
petitioner. There were no comments
received in response to the notice of
filing.
Section 408(b)(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
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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 performs a number of analyses to
determine the risks from aggregate
exposure to pesticide residues. First,
EPA determines the toxicity of
pesticides. Second, EPA examines
exposure to the pesticide through food,
drinking water, and through other
exposures that occur as a result of
pesticide use in residential settings.
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 ploymers 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. Toxicological Profile
Consistent with section 408(b)(2)(D)
of FFDCA, EPA has reviewed the
available scientific data and other
relevant information in support of this
action and considered its validity,
completeness and reliability and the
relationship of this information to
human risk. EPA has also considered
available information concerning the
variability of the sensitivities of major
identifiable subgroups of consumers,
including infants and children. The
nature of the toxic effects caused by
ammonium salts of fatty acids (C8-C18
saturated) are discussed in this unit.
The following provides a brief summary
of the risk assessment and conclusions
for the Agency’s review of ammonium
salts of fatty acids (C8-C18 saturated).
The Agency’s full decision document
for this action is available in the
Agency’s electronic docket
(regulations.gov) under the docket ID
number EPA–HQ–OPP–2008–0652.
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Ammonium salts of fatty acids are
mineral salts of naturally occurring fatty
acids found in the environment. Fatty
acids play a significant role in the
normal diet of humans, animals, and
plants and currently have Food and
Drug Administration and EPA approved
uses in food products. They are
naturally present in commonly eaten
fats and oils, accounting for
approximately 30 to 40% of the caloric
intake in the U.S. diet (~ 90 grams/day).
They are also found in cosmetics and
household cleaning products.
Ammonium salts of fatty acids have
shown to be of low toxicity via the oral
and dermal routes of exposure, Toxicity
category IV and III, respectively (40 CFR
156.62). When applied for long periods
of time, they have the potential to be
dermal irritants. In addition, ammonium
salts of fatty acids are eye irritants and
have the potential to cause permanent
eye injury. Limited data are available
regarding the inhalation toxicity of soap
salts; however, they are anticipated to
be irritating via the inhalation route of
exposure.
A subchronic range finding study did
not see any significant systemic toxicity
from nonanoic acid (C9 saturated) given
to rats at doses up to 1,834 milligrams/
kilograms/day (mg/kg/day). Ammonium
salts of fatty acids are not believed to be
mutagenic or carcinogenic. When used
at very high doses, potassium salts of
fatty acids (a chemical belonging to the
same chemical group) caused
reproductive effects (post-implantation
mortality at 6,000 mg/kg/day (6 times
the limit dose of 1,000 mg/kg/day) on
days 2 to 13 of pregnancy and musculoskeletal abnormalities observed at 600
mg/kg/day); however, studies on
ammonium salts of fatty acids did not
show developmental or mutagenic
effects in rats at doses up to 1,500 mg/
kg/day. In addition, no signs of
neurotoxicity or carcinogencity were
observed. Although reproductive/
developmental effects were seen at very
high doses in a study on a structurally
similar chemical, these effects were not
observed in studies on the actual inert
ingredient at doses up to 1,500 mg/kg/
day. Based on the available evidence the
Agency does not believe that
ammonium salt of fatty acids (C8-C18
saturated) when used as an inert
ingredient in pesticide products will
cause reproductive or developmental
effects. Due to the low toxicity of
ammonium soap salts and the natural
occurrence of fatty acids in the
environment and food products, a
chronic study was not required.
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V. Aggregate Exposures
In examining aggregate exposure,
section 408 of FFDCA directs EPA to
consider available information
concerning exposures from the pesticide
residue in food and all other nonoccupational exposures, including
drinking water from ground water or
surface water and exposure through
pesticide use in gardens, lawns, or
buildings (residential and other indoor
uses).
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.
Fatty acids are an essential
component of the mammalian diet and
the body is able to metabolize these
soap salts and use them as an energy
source. Due to the self-limiting nature of
these chemicals (e.g. unpleasant taste
and odor, herbicidal properties), their
natural occurrence in the environment,
their rapid environmental degradation
and low toxicity, and their presence in
commonly eaten foods (both naturally
and intentionally added), a quantitative
exposure assessment was not
performed. The anticipated exposure
from the use of ammonium salts of fatty
acids as inert ingredients in pesticide
products is expected to be minimal and
is not anticipated to significantly
increase the overall exposure to all
populations including infants and
children.
Because of their strong soil adsorption
and the rapid degradation of ammonium
salts of fatty acids they are not expected
to reach surface water via runoff nor are
they expected to leach into ground
water. Based on the physical/chemical
properties, volatilization from soils and
water is not expected. There is no
expected translocation into plants.
Ammonium salts of fatty acid are not
likely to persist in the environment and
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are expected to be indistinguishable
from naturally occurring ammonium
ions and fatty acids already present in
the environment as a result of plant
metabolism and formation by soil
microbes.
VI. Cumulative Effects
Section 408(b)(2)(D)(v) of FFDCA
requires that, when considering whether
to establish, modify, or revoke a
tolerance, the Agency consider
‘‘available information’’ concerning the
cumulative effects of a particular
pesticide’s residues and ‘‘other
substances that have a common
mechanism of toxicity.’’
Unlike other pesticides for which EPA
has followed a cumulative risk approach
based on a common mechanism of
toxicity, EPA has not made a common
mechanism of toxicity finding as to
ammonium salts of fatty acids (C8-C18
saturated) and any other substances, and
these chemicals do not appear to
produce a toxic metabolite produced by
other substances. For the purposes of
this tolerance action, therefore, EPA has
not assumed that these chemicals 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 the policy statements
released by EPA’s Office of Pesticide
Programs concerning common
mechanism determinations and
procedures for cumulating effects from
substances found to have a common
mechanism of toxicity on EPA’s website
at https://ww.epa.gov/pesticides/
cumulative/.
VII. Additional Safety Factor for the
Protection of Infants and Children.
Section 408 of the FFDCA provides
that EPA shall apply an additional
tenfold margin of exposure (safety) for
infants and children in the case of
threshold effects to account for prenatal
and postnatal toxicity and the
completeness of the data base unless
EPA determines that a different margin
of exposure (safety) will be safe for
infants and children. There was no
evidence of systemic toxicity or
developmental toxicity in rats at doses
up to 1,500 mg/kg/day in a
developmental toxicity study (Master
Record Identification Number
43843508) on pelargonic acid
(nonanoate acid). The study showed no
adverse effect of treatment on clinical
signs, body weights, weight gain, or
food/water consumption. No fetal
toxicity attributed to the effects of
treatment was observed between the
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treated (1,500 mg/kg/day) or the
untreated controls. Similarly, no
systemic toxicity was observed at doses
up to and including 1,837 mg/kg/day in
a 14–day toxicity study in rats. No
clinical signs of neurotoxicity were seen
in any of the repeat dose studies. Since
there was no hazard identified to adults
and developing fetuses EPA did not use
a safety factor analysis in assessing risks
to ammonium salts of fatty acids (C8-C18
saturated). For similar reasons, EPA
determined that an additional safety
factor to protect infants and children is
not needed.
VIII. Determination of Safety for U.S.
Population
IX. Other Considerations
A. Analytical Method
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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. Existing Exemptions
Ammonium stearate (C18 saturated;
CAS Reg. No. 1002–89–7), one of the
soap salts, has been approved as an inert
ingredient under 40 CFR 180.910. In
addition, 40 CFR 180.1284 established
an exemption from the requirement of a
tolerance for residues of the active
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C. International Tolerances
The Agency is not aware of any
country requiring a tolerance for
ammonium salts of fatty acids (C8-C18
saturated) nor have any CODEX
Maximum Residue Levels (MRLs) been
established for any food crops at this
time.
X. Conclusions
As noted in Unit IV, ammonium salts
of fatty acids are not expected to pose
an acute risk. Because of the low oral
and dermal toxicity, the rapid
degradation of the chemical, and the
natural presence of fatty acids in the
environment, the Agency concluded
that aggregate exposure will result in
minimal risk to all subpopulations,
including infants and children. Since
the inhalation route is not a likely
exposure pathway the anticipated risk
from inhalation exposure is also
considered minimal.
Taking into consideration all available
information on ammonium salts of fatty
acids (C8-C18 saturated), it has been
determined that there is a reasonable
certainty that no harm to any population
subgroup, including infants and
children, will result from aggregate
exposure to this chemical. Therefore,
the exemption from the requirement of
a tolerance for residues of ammonium
salts of fatty acids (C8-C18 saturated)
(CAS Reg. No. 5972–76–9, 63718–65–0,
16530–70–4, 32582–95–9, 2437–23–2,
191799–95–8, 16530–71–5, 93917–76–1,
5297–93–8, 94266–36–1, 1002–89–7),
when used as inert ingredient in preand post-harvest applications, under 40
CFR 180.910 can be considered safe
under section 408(q) of the FFDCA.
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ingredient ammonium salts of higher
fatty acids (C8-C18 saturated; C8-C12
unsaturated) in or on all food
commodities when applied for the
suppression and control of a wide
variety of grasses and weeds.
Therefore, a tolerance exemption is
established for Ammonium salts of fatty
acids (C8-C18 saturated) (CAS Reg. No.
5972–76–9, 63718–65–0, 16530–70–4,
32582–95–9, 2437–23–2, 191799–95–8,
16530–71–5, 93917–76–1, 5297–93–8,
94266–36–1, 1002–89–7) when used as
inert ingredient in pesticide
formulations applied to pre- and postharvest crops only.
XI. Statutory and Executive Order
Reviews
This final rule establishes a tolerance
under section 408(d) of FFDCA 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 final rule
has been exempted from review under
Executive Order 12866, this final rule 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 final rule 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 section 408(d) of FFDCA, such as
the exemption 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.
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This final rule 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 section 408(n)(4) of FFDCA. 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 final rule. In addition, this final
rule does not impose any enforceable
duty or contain any unfunded mandate
as described under Title II of the
Unfunded Mandates Reform Act of 1995
(UMRA) (Public Law 104–4).
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 of 1995
(NTTAA), Public Law 104–113, section
12(d) (15 U.S.C. 272 note).
XII. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report to each House of
the Congress and to the Comptroller
General of the United States. 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 this final rule in the
Federal Register. This final rule is not
a ‘‘major rule’’ as defined by 5 U.S.C.
804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
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Dated: March 11, 2010.
Lois Rossi,
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, in the table add
alphabetically the following inert
ingredient to read as follows:
■
§ 180.910 Inert ingredients used pre- and
post-harvest; exemptions from the
requirement of a tolerance.
*
*
*
*
*
Inert ingredients
*
*
*
Ammonium salts
of fatty acids
(C8-C18 saturated) (CAS
Reg. No. 5972–
76–9, 63718–
65–0, 16530–
70–4, 32582–
95–9, 2437–23–
2, 191799–95–
8, 16530–71–5,
93917–76–1,
5297–93–8,
94266–36–1,
1002–89–7)
*
*
*
Limits
*
Uses
*
*
*
Surfactant
for hearings must be received on or
before May 24, 2010, 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: EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPP–2009–0092. All documents in the
docket are listed in the docket index
available at https://www.regulations.gov.
Although listed in the index, some
information is not publicly available,
e.g., Confidential Business Information
(CBI) or other information whose
disclosure is restricted by statute.
Certain other material, such as
copyrighted material, is not placed on
the Internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available in the electronic docket at
https://www.regulations.gov, or, if only
available in hard copy, at the OPP
Regulatory Public Docket in Rm. S–
4400, One Potomac Yard (South Bldg.),
2777 S. Crystal Dr., Arlington, VA. The
Docket Facility is open from 8:30 a.m.
to 4 p.m., Monday through Friday,
excluding legal holidays. The Docket
Facility telephone number is (703) 305–
5805.
[FR Doc. 2010–6495 Filed 3–23–10; 8:45 am]
FOR FURTHER INFORMATION CONTACT:
Laura Nollen, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(703) 305–7390; e-mail address:
nollen.laura@epa.gov.
BILLING CODE 6560–50–S
SUPPLEMENTARY INFORMATION:
*
*
*
*
I. General Information
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2009–0092; FRL–8814–2]
Clopyralid; Pesticide Tolerances
WReier-Aviles on DSKGBLS3C1PROD with RULES
AGENCY: Environmental Protection
Agency (EPA).
ACTION: Final rule.
SUMMARY: This regulation establishes
tolerances for residues of clopyralid in
or on Swiss chard and bushberry
subgroup 13-07B. This regulation
additionally amends an existing
tolerance in or on strawberry.
Interregional Research Project Number 4
(IR-4) requested these tolerances under
the Federal Food, Drug, and Cosmetic
Act (FFDCA).
DATES: This regulation is effective
March 24, 2010. Objections and requests
VerDate Nov<24>2008
14:43 Mar 23, 2010
Jkt 220001
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. Potentially
affected entities may include, but are
not limited to those engaged in the
following activities:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
This listing is not intended to be
exhaustive, but rather to provide a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
PO 00000
Frm 00018
Fmt 4700
Sfmt 4700
assist you and others in determining
whether this action might apply to
certain entities. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
B. How Can I Get Electronic Access to
Other Related Information?
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Printing Office’s e-CFR
cite at https://www.gpoaccess.gov/ecfr.
To access the OPPTS harmonized test
guidelines referenced in this document
electronically, please go to https://
www.epa.gpo/oppts and select ‘‘Test
Methods and Guidelines.’’
C. Can I File an Objection or Hearing
Request?
Under section 408(g) of FFDCA, 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–2009–0092 in the subject line on
the first page of your submission. All
requests must be in writing, and must be
mailed or delivered to the Hearing Clerk
as required by 40 CFR part 178 on or
before May 24, 2010.
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 that does not
contain any CBI for inclusion in the
public docket that is described in
ADDRESSES. Information not marked
confidential pursuant to 40 CFR part 2
may be disclosed publicly by EPA
without prior notice. Submit this copy,
identified by docket ID number EPA–
HQ–OPP–2009–0092, by one of the
following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
instructions for submitting comments.
• Mail: Office of Pesticide Programs
(OPP) Regulatory Public Docket (7502P),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001.
• Delivery: OPP Regulatory Public
Docket (7502P), Environmental
Protection Agency, Rm. S–4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. Deliveries
are only accepted during the Docket
Facility’s normal hours of operation
(8:30 a.m. to 4 p.m., Monday through
Friday, excluding legal holidays).
E:\FR\FM\24MRR1.SGM
24MRR1
Agencies
[Federal Register Volume 75, Number 56 (Wednesday, March 24, 2010)]
[Rules and Regulations]
[Pages 14082-14086]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-6495]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2008-0652; FRL-8809-6]
Ammonium Salts of Fatty Acids (C8-C18
Saturated); 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 ammonium salts of fatty acids
(C8-C18 saturated) applied pre- and post-harvest
on all raw agricultural commodities when applied/used as a surfactant.
Falcon Lab, LLC. submitted a petition to EPA under the Federal Food,
Drug, and Cosmetic Act (FFDCA), requesting an exemption from the
requirement of a tolerance. This regulation eliminates the need to
establish a maximum permissible level for residues of ammonium salts of
fatty acids (C8-C18 saturated).
DATES: This regulation is effective March 24, 2010. Objections and
requests for hearings must be received on or before May 24, 2010, 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: EPA has established a docket for this action under docket
identification (ID) number EPA-HQ-OPP-2008-0652. All documents in the
docket are listed in the docket index available at https://www.regulations.gov. Although listed in the index, some information is
not publicly available, e.g., Confidential Business Information (CBI)
or other information whose disclosure is restricted by statute. Certain
other material, such as copyrighted material, is not placed on the
Internet and will be publicly available only in hard copy form.
Publicly available docket materials are available in the electronic
docket at https://www.regulations.gov, or, if only available in hard
copy, at the OPP Regulatory Public Docket in Rm. S-4400, One Potomac
Yard (South Bldg.), 2777 S. Crystal Dr., Arlington, VA. The Docket
Facility is open from 8:30 a.m. to 4 p.m., Monday through Friday,
excluding legal holidays. The Docket Facility telephone number is (703)
305-5805.
FOR FURTHER INFORMATION CONTACT: Deirdre Sunderland, Registration
Division (7505P), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-
0001; telephone number: (703) 603-0851; e-mail address:
sunderland.deirdre@epa.gov.
SUPPLEMENTARY INFORMATION:
[[Page 14083]]
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.
Potentially affected entities may include, but are not limited to:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. Other types of entities not listed in this unit could also be
affected. The North American Industrial Classification System (NAICS)
codes have been provided to assist you and others in determining
whether this action might apply to certain entities. If you have any
questions regarding the applicability of this action to a particular
entity, consult the person listed under FOR FURTHER INFORMATION
CONTACT.
B. How Can I Access Electronic Copies of This Document?
You may access a frequently updated electronic version of 40 CFR
part 180 through the Government Printing Office's e-CFR cite at https://www.gpoaccess.gov/ecfr.
C. Can I File an Objection or Hearing Request?
Under section 408(g) of FFDCA, 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. The EPA procedural regulations which
govern the submission of objections and requests for hearings appear in
40 CFR part 178. 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-2008-0652 in the subject line on the first page of
your submission. All requests must be in writing, and must be mailed or
delivered to the Hearing Clerk on or before May 24, 2010.
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 that does not contain any CBI for inclusion in the public
docket that is described in ADDRESSES. Information not marked
confidential pursuant to 40 CFR part 2 may be disclosed publicly by EPA
without prior notice. Submit your copies, identified by docket ID
number EPA-HQ-OPP-2008-0652, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the on-line instructions for submitting comments.
Mail: Office of Pesticide Programs (OPP) Regulatory Public
Docket (7502P), Environmental Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001.
Delivery: OPP Regulatory Public Docket (7502P),
Environmental Protection Agency, Rm. S-4400, One Potomac Yard (South
Bldg.), 2777 S. Crystal Dr., Arlington, VA. Deliveries are only
accepted during the Docket Facility's normal hours of operation (8:30
a.m. to 4 p.m., Monday through Friday, excluding legal holidays).
Special arrangements should be made for deliveries of boxed
information. The Docket Facility telephone number is (703) 305-5805.
II. Background and Statutory Findings
In the Federal Register of September 5, 2008 (73 FR 51817) (FRL-
8380-4), EPA issued a notice pursuant to section 408 of FFDCA, 21
U.S.C. 346a, as amended by the Food Quality Protection ACT (FQPA)
(Public Law 104-170), announcing the filing of a pesticide petition (PP
8E7402) by Falcon Lab, LLC, 1103 Norbee Drive, Wilmington, DE 19803.
The petition requested that 40 CFR 180.910 be amended by establishing
an exemption from the requirement of a tolerance for residues of
ammonium salts of fatty acids (C8-C18 saturated)
when used as an inert ingredient in pesticide formulations applied pre-
and post-harvest. A request for a tolerance exemption under 40 CFR
180.950 was withdrawn by the company. That notice included a summary of
the petition prepared by the petitioner. There were no comments
received in response to the notice of filing.
Section 408(b)(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 performs a number of analyses to determine the risks from
aggregate exposure to pesticide residues. First, EPA determines the
toxicity of pesticides. Second, EPA examines exposure to the pesticide
through food, drinking water, and through other exposures that occur as
a result of pesticide use in residential settings.
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 ploymers 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. Toxicological Profile
Consistent with section 408(b)(2)(D) of FFDCA, EPA has reviewed the
available scientific data and other relevant information in support of
this action and considered its validity, completeness and reliability
and the relationship of this information to human risk. EPA has also
considered available information concerning the variability of the
sensitivities of major identifiable subgroups of consumers, including
infants and children. The nature of the toxic effects caused by
ammonium salts of fatty acids (C8-C18 saturated)
are discussed in this unit. The following provides a brief summary of
the risk assessment and conclusions for the Agency's review of ammonium
salts of fatty acids (C8-C18 saturated). The
Agency's full decision document for this action is available in the
Agency's electronic docket (regulations.gov) under the docket ID number
EPA-HQ-OPP-2008-0652.
[[Page 14084]]
Ammonium salts of fatty acids are mineral salts of naturally
occurring fatty acids found in the environment. Fatty acids play a
significant role in the normal diet of humans, animals, and plants and
currently have Food and Drug Administration and EPA approved uses in
food products. They are naturally present in commonly eaten fats and
oils, accounting for approximately 30 to 40% of the caloric intake in
the U.S. diet (~ 90 grams/day). They are also found in cosmetics and
household cleaning products.
Ammonium salts of fatty acids have shown to be of low toxicity via
the oral and dermal routes of exposure, Toxicity category IV and III,
respectively (40 CFR 156.62). When applied for long periods of time,
they have the potential to be dermal irritants. In addition, ammonium
salts of fatty acids are eye irritants and have the potential to cause
permanent eye injury. Limited data are available regarding the
inhalation toxicity of soap salts; however, they are anticipated to be
irritating via the inhalation route of exposure.
A subchronic range finding study did not see any significant
systemic toxicity from nonanoic acid (C9 saturated) given to
rats at doses up to 1,834 milligrams/kilograms/day (mg/kg/day).
Ammonium salts of fatty acids are not believed to be mutagenic or
carcinogenic. When used at very high doses, potassium salts of fatty
acids (a chemical belonging to the same chemical group) caused
reproductive effects (post-implantation mortality at 6,000 mg/kg/day (6
times the limit dose of 1,000 mg/kg/day) on days 2 to 13 of pregnancy
and musculo-skeletal abnormalities observed at 600 mg/kg/day); however,
studies on ammonium salts of fatty acids did not show developmental or
mutagenic effects in rats at doses up to 1,500 mg/kg/day. In addition,
no signs of neurotoxicity or carcinogencity were observed. Although
reproductive/developmental effects were seen at very high doses in a
study on a structurally similar chemical, these effects were not
observed in studies on the actual inert ingredient at doses up to 1,500
mg/kg/day. Based on the available evidence the Agency does not believe
that ammonium salt of fatty acids (C8-C18
saturated) when used as an inert ingredient in pesticide products will
cause reproductive or developmental effects. Due to the low toxicity of
ammonium soap salts and the natural occurrence of fatty acids in the
environment and food products, a chronic study was not required.
V. Aggregate Exposures
In examining aggregate exposure, section 408 of FFDCA directs EPA
to consider available information concerning exposures from the
pesticide residue in food and all other non-occupational exposures,
including drinking water from ground water or surface water and
exposure through pesticide use in gardens, lawns, or buildings
(residential and other indoor uses).
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.
Fatty acids are an essential component of the mammalian diet and
the body is able to metabolize these soap salts and use them as an
energy source. Due to the self-limiting nature of these chemicals (e.g.
unpleasant taste and odor, herbicidal properties), their natural
occurrence in the environment, their rapid environmental degradation
and low toxicity, and their presence in commonly eaten foods (both
naturally and intentionally added), a quantitative exposure assessment
was not performed. The anticipated exposure from the use of ammonium
salts of fatty acids as inert ingredients in pesticide products is
expected to be minimal and is not anticipated to significantly increase
the overall exposure to all populations including infants and children.
Because of their strong soil adsorption and the rapid degradation
of ammonium salts of fatty acids they are not expected to reach surface
water via runoff nor are they expected to leach into ground water.
Based on the physical/chemical properties, volatilization from soils
and water is not expected. There is no expected translocation into
plants. Ammonium salts of fatty acid are not likely to persist in the
environment and are expected to be indistinguishable from naturally
occurring ammonium ions and fatty acids already present in the
environment as a result of plant metabolism and formation by soil
microbes.
VI. Cumulative Effects
Section 408(b)(2)(D)(v) of FFDCA requires that, when considering
whether to establish, modify, or revoke a tolerance, the Agency
consider ``available information'' concerning the cumulative effects of
a particular pesticide's residues and ``other substances that have a
common mechanism of toxicity.''
Unlike other pesticides for which EPA has followed a cumulative
risk approach based on a common mechanism of toxicity, EPA has not made
a common mechanism of toxicity finding as to ammonium salts of fatty
acids (C8-C18 saturated) and any other
substances, and these chemicals do not appear to produce a toxic
metabolite produced by other substances. For the purposes of this
tolerance action, therefore, EPA has not assumed that these chemicals
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 the policy statements released by EPA's Office of
Pesticide Programs concerning common mechanism determinations and
procedures for cumulating effects from substances found to have a
common mechanism of toxicity on EPA's website at https://ww.epa.gov/pesticides/cumulative/.
VII. Additional Safety Factor for the Protection of Infants and
Children.
Section 408 of the FFDCA provides that EPA shall apply an
additional tenfold margin of exposure (safety) for infants and children
in the case of threshold effects to account for prenatal and postnatal
toxicity and the completeness of the data base unless EPA determines
that a different margin of exposure (safety) will be safe for infants
and children. There was no evidence of systemic toxicity or
developmental toxicity in rats at doses up to 1,500 mg/kg/day in a
developmental toxicity study (Master Record Identification Number
43843508) on pelargonic acid (nonanoate acid). The study showed no
adverse effect of treatment on clinical signs, body weights, weight
gain, or food/water consumption. No fetal toxicity attributed to the
effects of treatment was observed between the
[[Page 14085]]
treated (1,500 mg/kg/day) or the untreated controls. Similarly, no
systemic toxicity was observed at doses up to and including 1,837 mg/
kg/day in a 14-day toxicity study in rats. No clinical signs of
neurotoxicity were seen in any of the repeat dose studies. Since there
was no hazard identified to adults and developing fetuses EPA did not
use a safety factor analysis in assessing risks to ammonium salts of
fatty acids (C8-C18 saturated). For similar
reasons, EPA determined that an additional safety factor to protect
infants and children is not needed.
VIII. Determination of Safety for U.S. Population
As noted in Unit IV, ammonium salts of fatty acids are not expected
to pose an acute risk. Because of the low oral and dermal toxicity, the
rapid degradation of the chemical, and the natural presence of fatty
acids in the environment, the Agency concluded that aggregate exposure
will result in minimal risk to all subpopulations, including infants
and children. Since the inhalation route is not a likely exposure
pathway the anticipated risk from inhalation exposure is also
considered minimal.
Taking into consideration all available information on ammonium
salts of fatty acids (C8-C18 saturated), it has
been determined that there is a reasonable certainty that no harm to
any population subgroup, including infants and children, will result
from aggregate exposure to this chemical. Therefore, the exemption from
the requirement of a tolerance for residues of ammonium salts of fatty
acids (C8-C18 saturated) (CAS Reg. No. 5972-76-9,
63718-65-0, 16530-70-4, 32582-95-9, 2437-23-2, 191799-95-8, 16530-71-5,
93917-76-1, 5297-93-8, 94266-36-1, 1002-89-7), when used as inert
ingredient in pre- and post-harvest applications, under 40 CFR 180.910
can be considered safe under section 408(q) of the FFDCA.
IX. Other Considerations
A. Analytical Method
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. Existing Exemptions
Ammonium stearate (C18 saturated; CAS Reg. No. 1002-89-
7), one of the soap salts, has been approved as an inert ingredient
under 40 CFR 180.910. In addition, 40 CFR 180.1284 established an
exemption from the requirement of a tolerance for residues of the
active ingredient ammonium salts of higher fatty acids (C8-
C18 saturated; C8-C12 unsaturated) in
or on all food commodities when applied for the suppression and control
of a wide variety of grasses and weeds.
C. International Tolerances
The Agency is not aware of any country requiring a tolerance for
ammonium salts of fatty acids (C8-C18 saturated)
nor have any CODEX Maximum Residue Levels (MRLs) been established for
any food crops at this time.
X. Conclusions
Therefore, a tolerance exemption is established for Ammonium salts
of fatty acids (C8-C18 saturated) (CAS Reg. No.
5972-76-9, 63718-65-0, 16530-70-4, 32582-95-9, 2437-23-2, 191799-95-8,
16530-71-5, 93917-76-1, 5297-93-8, 94266-36-1, 1002-89-7) when used as
inert ingredient in pesticide formulations applied to pre- and post-
harvest crops only.
XI. Statutory and Executive Order Reviews
This final rule establishes a tolerance under section 408(d) of
FFDCA 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 final rule has been
exempted from review under Executive Order 12866, this final rule 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 final rule 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 section 408(d) of FFDCA, such as the exemption 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 final rule 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 section 408(n)(4) of FFDCA. 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 final rule. In addition,
this final rule does not impose any enforceable duty or contain any
unfunded mandate as described under Title II of the Unfunded Mandates
Reform Act of 1995 (UMRA) (Public Law 104-4).
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 of 1995 (NTTAA), Public Law 104-113, section 12(d) (15 U.S.C. 272
note).
XII. Congressional Review Act
The Congressional Review Act, 5 U.S.C. 801 et seq., generally
provides that before a rule may take effect, the agency promulgating
the rule must submit a rule report to each House of the Congress and to
the Comptroller General of the United States. 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 this final rule in the Federal
Register. This final rule is not a ``major rule'' as defined by 5
U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
[[Page 14086]]
Dated: March 11, 2010.
Lois Rossi,
Director, Registration Division, Office of Pesticide Programs.
0
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, in the table add alphabetically the following inert
ingredient 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
------------------------------------------------------------------------
* * * * * * *
Ammonium salts of fatty acids Surfactant
(C8-C18 saturated) (CAS Reg.
No. 5972-76-9, 63718-65-0,
16530-70-4, 32582-95-9, 2437-23-
2, 191799-95-8, 16530-71-5,
93917-76-1, 5297-93-8, 94266-36-
1, 1002-89-7)
* * * * * * *
------------------------------------------------------------------------
[FR Doc. 2010-6495 Filed 3-23-10; 8:45 am]
BILLING CODE 6560-50-S