Ethaboxam; Pesticide Tolerances, 2725-2728 [2022-00854]
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Federal Register / Vol. 87, No. 12 / Wednesday, January 19, 2022 / Rules and Regulations
• Does not impose an information
collection burden under the provisions
of the Paperwork Reduction Act (44
U.S.C. 3501 et seq.);
• Is certified as not having a
significant economic impact on a
substantial number of small entities
under the Regulatory Flexibility Act (5
U.S.C. 601 et seq.);
• Does not contain any unfunded
mandate or significantly or uniquely
affect small governments, as described
in the Unfunded Mandates Reform Act
of 1995 (Pub. L. 104–4);
• Does not have Federalism
implications as specified in Executive
Order 13132 (64 FR 43255, August 10,
1999);
• Is not an economically significant
regulatory action based on health or
safety risks subject to Executive Order
13045 (62 FR 19885, April 23, 1997);
• Is not a significant regulatory action
subject to Executive Order 13211 (66 FR
28355, May 22, 2001);
• Is not subject to requirements of
section 12(d) of the National
Technology Transfer and Advancement
Act of 1995 (15 U.S.C. 272 note) because
application of those requirements would
be inconsistent with the CAA; and
• Does not provide EPA with the
discretionary authority to address, as
appropriate, disproportionate human
health or environmental effects, using
practicable and legally permissible
methods, under Executive Order 12898
(59 FR 7629, February 16, 1994).
In addition, this rule does not have
tribal implications as specified by
Executive Order 13175 (65 FR 67249,
November 9, 2000), because the SIP is
Name of non-regulatory
SIP revision
not approved to apply in Indian country
located in the State, and EPA notes that
it will not impose substantial direct
costs on tribal governments or preempt
tribal law.
B. Submission to Congress and the
Comptroller General
The Congressional Review Act, 5
U.S.C. 801 et seq., as added by the Small
Business Regulatory Enforcement
Fairness Act of 1996, generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of the
Congress and to the Comptroller General
of the United States. EPA will submit a
report containing this action 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. A major rule
cannot take effect until 60 days after it
is published in the Federal Register.
This action is not a ‘‘major rule’’ as
defined by 5 U.S.C. 804(2).
C. Petitions for Judicial Review
Under section 307(b)(1) of the CAA,
petitions for judicial review of this
action must be filed in the United States
Court of Appeals for the appropriate
circuit by March 21, 2022. Filing a
petition for reconsideration by the
Administrator of this final rule does not
affect the finality of this action for the
purposes of judicial review nor does it
extend the time within which a petition
for judicial review may be filed and
shall not postpone the effectiveness of
Applicable geographic area
State
submittal
date
*
*
*
Emissions Statement Certifi- Delaware’s portion of the Philacation for the 2015 Ozone
delphia-Wilmington-Atlantic
National Ambient Air QualCity, PA-NJ-MD-DE 2015
ity Standard.
ozone NAAQS nonattainment area (i.e., New Castle
County).
[FR Doc. 2022–00976 Filed 1–18–22; 8:45 am]
BILLING CODE 6560–50–P
*
8/3/20
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Environmental Protection
Agency (EPA).
Fmt 4700
For the reasons stated in the
preamble, the EPA amends 40 CFR part
52 as follows:
PART 52—APPROVAL AND
PROMULGATION OF
IMPLEMENTATION PLANS
1. The authority citation for part 52
continues to read as follows:
■
Authority: 42 U.S.C. 7401 et seq.
Subpart I—Delaware
2. In § 52.420, the table in paragraph
(e) is amended by adding an entry for
‘‘Emissions Statement Certification for
the 2015 Ozone National Ambient Air
Quality Standard’’ at the end of the table
to read as follows:
■
§ 52.420
*
Identification of plan.
*
*
(e) * * *
ACTION:
*
*
Final rule.
This regulation establishes
tolerances for residues of ethaboxam in
or on Brassica, leafy greens, subgroup
4–16B and Vegetable, Brassica, head
and stem, group 5–16. The Interregional
Research Project Number 4 (IR–4)
requested these tolerance actions under
the Federal Food, Drug, and Cosmetic
Act (FFDCA).
SUMMARY:
AGENCY:
Frm 00053
Dated: January 10, 2022.
Diana Esher,
Acting Regional Administrator, Region III.
*
*
Certification that Delaware’s SIP-approved regulations under 7 DE Administrative Code 1117 Section 7.0
meet the emissions statements requirements
of
CAA
Section
182(a)(3)(B) for the 2008 ozone
NAAQS.
ENVIRONMENTAL PROTECTION
AGENCY
PO 00000
Environmental protection, Air
pollution control, Incorporation by
reference, Intergovernmental relations,
Nitrogen dioxide, Ozone, Reporting and
recordkeeping requirements, Volatile
organic compounds.
*
1/19/2022, [insert Federal Register citation].
Ethaboxam; Pesticide Tolerances
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List of Subjects in 40 CFR Part 52
Additional
explanation
[EPA–HQ–OPP–2021–0045; FRL–9331–01–
OCSPP]
16:00 Jan 18, 2022
such rule or action. This action
approving Delaware’s emissions
statement certification for the 2015
ozone NAAQS may not be challenged
later in proceedings to enforce its
requirements. (See section 307(b)(2).)
EPA approval date
40 CFR Part 180
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Federal Register / Vol. 87, No. 12 / Wednesday, January 19, 2022 / Rules and Regulations
This regulation is effective
January 19, 2022. Objections and
requests for hearings must be received
on or before March 21, 2022, 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–2021–0045, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805.
Due to the public health concerns
relating to COVID–19, the EPA Docket
Center (EPA/DC) and Reading Room is
closed to visitors with limited
exceptions. The staff continues to
provide customer service via email,
phone, and webform. For the latest
status information on EPA/DC services,
docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Marietta Echeverria, Acting Director,
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.
DATES:
SUPPLEMENTARY INFORMATION:
I. General Information
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A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
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16:00 Jan 18, 2022
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B. How can I get electronic access to
other relatedinformation?
II. Summary of Petitioned-For
Tolerance
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Office of the Federal Register’s eCFR site at https://www.ecfr.gov/
current/title-40.
In the Federal Register of March 22,
2021 (86 FR 15162) (FRL–10021–44)
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide petition (PP 0E8871) by IR–4,
North Carolina State University, 1730
Varsity Drive, Venture IV, Suite 210,
Raleigh, NC 27606. The petition
requested to establish tolerances in 40
CFR 180.622 for residues of the
fungicide ethaboxam, (N-(cyano-2thienylmethyl)-4-ethyl-2-(ethylamino)5-thiazolecarboxamide) in or on
Brassica, leafy greens, subgroup 4–16B
at 7 parts per million (ppm) and
Vegetable, Brassica, head and stem,
group 5–16 at 3 ppm. That document
referenced a summary of the petition
prepared by IR–4, the petitioner, which
is available in the docket, https://
www.regulations.gov. There were no
comments received in response to the
notice of filing.
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a(g), any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2021–0045 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 March
21, 2022. 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–
2021–0045, 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/where-sendcomments-epa-dockets.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
PO 00000
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III. Aggregate Risk Assessment and
Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA
allows EPA to establish a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(b)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings but does not include
occupational exposure. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing a
tolerance and to ‘‘ensure that there is a
reasonable certainty that no harm will
result to infants and children from
aggregate exposure to the pesticide
chemical residue. . . . ’’
Consistent with FFDCA section
408(b)(2)(D), and the factors specified
therein, EPA has reviewed the available
scientific data and other relevant
information in support of this action.
EPA has sufficient data to assess the
hazards of and to make a determination
on aggregate exposure for ethaboxam
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with ethaboxam follows.
In an effort to streamline its
publications in the Federal Register,
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Federal Register / Vol. 87, No. 12 / Wednesday, January 19, 2022 / Rules and Regulations
EPA is not reprinting sections that
repeat what has been previously
published for tolerance rulemakings of
the same pesticide chemical. Where
scientific information concerning a
particular chemical remains unchanged,
the content of those sections would not
vary between tolerance rulemaking, and
EPA considers referral back to those
sections as sufficient to provide an
explanation of the information EPA
considered in making its safety
determination for the new rulemaking.
EPA has previously published
tolerance rulemakings for ethaboxam, in
which EPA concluded, based on the
available information, that there is a
reasonable certainty that no harm would
result from aggregate exposure to
ethaboxam and established tolerances
for residues of that chemical. EPA is
incorporating previously published
sections from those rulemakings that
remain unchanged as described further
in this rulemaking.
Toxicological profile. For a discussion
of the Toxicological Profile of
ethaboxam, see Unit III.A. of the
ethaboxam tolerance rulemaking
published in the Federal Register of
August 3, 2017 (82 FR 36086) (FRL–
9961–69).
Toxicological points of departure/
Levels of concern. For a summary of the
Toxicological Points of Departure/
Levels of Concern for ethaboxam used
for human risk assessment, see Unit
III.B. of the August 3, 2017 ethaboxam
tolerance rulemaking.
Exposure assessment. Much of the
exposure assessment remains
unchanged from the previous
rulemaking, although the exposure
assessment has been updated to include
the petitioned-for tolerances based on
the same previous assumptions of
tolerance level residues and 100 percent
crop treated (PCT). Additionally, the
estimated drinking water concentration
is the same as that used in the previous
assessment (7.4 ppb) for the chronic
assessment (the only dietary assessment
needed). There are no residential uses
for ethaboxam, therefore no short- or
intermediate-term exposure is expected.
For a description of the previous
approach to and assumptions for the
exposure assessment, please reference
Unit III.C. of the August 3, 2017
rulemaking.
Safety factor for infants and children.
EPA continues to conclude that there
are reliable data to support the
reduction of the Food Quality Protection
Act (FQPA) safety factor. See Unit III.D.
of the August 3, 2017 rulemaking for a
discussion of the Agency’s rationale for
that determination.
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Aggregate risks and Determination of
safety. EPA determines whether acute
and chronic dietary pesticide exposures
are safe by comparing aggregate
exposure estimates to the acute
population adjusted dose (aPAD) and
chronic population adjusted dose
(cPAD). Short-, intermediate-, and
chronic risks are evaluated by
comparing the estimated aggregate food,
water, and residential exposure to the
appropriate points of departure to
ensure that an adequate margin of
exposure (MOE) exists. For linear cancer
risks, EPA calculates the lifetime
probability of acquiring cancer given the
estimated aggregate exposure.
An acute endpoint attributable to a
single dose exposure was not identified;
therefore, an acute dietary risk
assessment was not conducted. Chronic
dietary risks are below the Agency’s
level of concern of 100% of the cPAD;
they are 39% of the cPAD for children
1 to 2 years old, the group with the
highest estimated exposure. As the
chronic dietary endpoint and dose are
protective of potential cancer effects,
ethaboxam is not expected to pose a
dietary or aggregate cancer risk of
concern.
Therefore, based on the risk
assessments and information described
above, EPA concludes there is a
reasonable certainty that no harm will
result to the general population, or to
infants and children, from aggregate
exposure to ethaboxam residues. More
detailed information on this action can
be found in the document entitled,
‘‘Ethaboxam. Human Health Risk
Assessment for the Proposed New Uses
on Brassica Head and Stem Vegetable
Crop Group 5–16 and Brassica Leafy
Greens Crop Subgroup 4–16B’’ by going
to the docket established by this action,
EPA–HQ–OPP–2021–0045.
IV. Other Considerations
A. Analytical Enforcement Methodology
For a discussion of the available
analytical enforcement method, see Unit
IV.A. of the August 3, 2017 rulemaking.
B. International Residue Limits
In making its tolerance decisions, EPA
seeks to harmonize U.S. tolerances with
international standards whenever
possible, consistent with U.S. food
safety standards and agricultural
practices. EPA considers the
international maximum residue limits
(MRLs) established by the Codex
Alimentarius Commission (Codex), as
required by FFDCA section 408(b)(4).
Codex does not have established
MRLs for ethaboxam in commodities
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2727
that are members of subgroup 4–16B or
group 5–16.
V. Conclusion
Therefore, tolerances are established
for residues of ethaboxam in or on
Brassica, leafy greens, subgroup 4–16B
at 7 ppm and Vegetable, Brassica, head
and stem, group 5–16 at 3 ppm.
VI. Statutory and Executive Order
Reviews
This action establishes tolerances
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001), or to
Executive Order 13045, entitled
‘‘Protection of Children from
Environmental Health Risks and Safety
Risks’’ (62 FR 19885, April 23, 1997).
This action does not contain any
information collections subject to OMB
approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et
seq.), nor does it require any special
considerations under Executive Order
12898, entitled ‘‘Federal Actions to
Address Environmental Justice in
Minority Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerances in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or Tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
has determined that this action will not
have a substantial direct effect on States
or Tribal Governments, on the
relationship between the National
Government and the States or Tribal
Governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
Tribes. Thus, the Agency has
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Federal Register / Vol. 87, No. 12 / Wednesday, January 19, 2022 / Rules and Regulations
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).
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: December 29, 2021.
Daniel Rosenblatt,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, for the reasons stated in the
preamble, EPA is amending 40 CFR
chapter 1 as follows:
PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
CHEMICAL RESIDUES IN FOOD
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Amend § 180.622, by adding in
alphabetical order to table 1 to
paragraph (a) the entries ‘‘Brassica, leafy
greens, subgroup 4–16B’’ and
‘‘Vegetable, Brassica, head and stem,
group 5–16’’ to read as follows:
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§ 180.622 Ethaboxam; tolerances for
residues.
(a) * * *
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Parts per
million
Commodity
*
*
*
*
Brassica, leafy greens, subgroup 4–16B
*
*
*
*
*
Vegetable, Brassica, head and stem,
group 5–16 ...........................................
*
*
*
*
*
7
3
*
[FR Doc. 2022–00854 Filed 1–18–22; 8:45 am]
BILLING CODE 6560–50–P
CORPORATION FOR NATIONAL AND
COMMUNITY SERVICE
45 CFR Parts 1230 and 2554
RIN 3045–AA82
VII. Congressional Review Act
■
TABLE 1 TO PARAGRAPH (a)
Annual Civil Monetary Penalties
Inflation Adjustment
Corporation for National and
Community Service.
ACTION: Final rule.
AGENCY:
The Corporation for National
and Community Service (operating as
AmeriCorps) is updating its regulations
to reflect required annual inflationrelated increases to the civil monetary
penalties under the Federal Civil
Penalties Inflation Adjustment Act
Improvements Act of 2015 (Act) and
Office of Management and Budget
(OMB) guidance.
DATES: This rule is effective January 19,
2022.
FOR FURTHER INFORMATION CONTACT:
Kiara Rhodes, Office of General
Counsel, at PublicComments@cns.gov or
at 202–937–6965.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
AmeriCorps, the operating name for
Corporation for National and
Community Service, is a Federal agency
that engages millions of Americans in
service. AmeriCorps members and
AmeriCorps Seniors volunteers serve
directly with nonprofit organizations to
tackle our Nation’s most pressing
challenges. For more information, visit
americorps.gov.
AmeriCorps has two civil monetary
penalties in its regulations. A civil
monetary penalty under the Act is a
penalty, fine, or other sanction that: (1)
Is for a specific monetary amount as
provided by Federal law or has a
maximum amount provided for by
Federal law; and (2) is assessed or
enforced by an agency pursuant to
Federal law; and (3) is assessed or
PO 00000
Frm 00056
Fmt 4700
Sfmt 4700
enforced pursuant to an administrative
proceeding or a civil action in the
Federal courts. (See 28 U.S.C. 2461
note). A civil monetary penalty does not
include a penalty levied for violation of
a criminal statute, or fees for services,
licenses, permits, or other regulatory
review.
The Federal Civil Penalties Inflation
Adjustment Act Improvements Act of
2015 (Sec. 701 of Pub. L. 114–74) (the
‘‘Act’’) requires agencies to adjust their
civil monetary penalties for inflation
annually. This rule updates
AmeriCorps’ two civil penalties for
inflation.
II. Method of Calculation
The inflation adjustment for each
applicable civil monetary penalty is
determined using the percent increase
in the Consumer Price Index for all
Urban Consumers (CPI–U) for the month
of October of the year in which the
amount of each civil money penalty was
most recently established or modified.
See December 15, 2021, OMB Memo for
the Heads of Executive Departments and
Agencies, M–22–07, Implementation of
Penalty Inflation Adjustments for 2022,
Pursuant to the Federal Civil Penalties
Inflation Adjustment Act Improvements
Act of 2015. The cost-of-living
adjustment multiplier for 2022, based
on the CPI–U for the month of October
2021, not seasonally adjusted, is
1.06222.
The agency identified two civil
penalties in its regulations: (1) The
penalty associated with Restrictions on
Lobbying (45 CFR 1230.400) and (2) the
penalty associated with the Program
Fraud Civil Remedies Act (45 CFR
2554.1):
• The civil monetary penalties related
to Restrictions on Lobbying (45 CFR
1230.400) range from $20,732 to
$207,313. Using the 2022 multiplier, the
new range of possible civil monetary
penalties is from $22,022 to $220,212.
• The Program Fraud Civil Remedies
Act of 1986 (45 CFR 2554.1) civil
monetary penalty has an upper limit of
$11,803. Using the 2022 multiplier, the
new upper limit of the civil monetary
penalty is $12,537.
III. Summary of Final Rule
This final rule adjusts the civil
monetary penalty amounts related to
Restrictions on Lobbying (45 CFR
1230.400) and the Program Fraud Civil
Remedies Act of 1986 (45 CFR 2554.1).
The range of civil monetary penalties
related to Restrictions on Lobbying
increase from ‘‘$20,732 to $207,313’’ to
‘‘$22,022 to $220,212.’’ The civil
monetary penalties for the Program
Fraud Civil Remedies Act of 1986
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Agencies
[Federal Register Volume 87, Number 12 (Wednesday, January 19, 2022)]
[Rules and Regulations]
[Pages 2725-2728]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-00854]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2021-0045; FRL-9331-01-OCSPP]
Ethaboxam; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes tolerances for residues of
ethaboxam in or on Brassica, leafy greens, subgroup 4-16B and
Vegetable, Brassica, head and stem, group 5-16. The Interregional
Research Project Number 4 (IR-4) requested these tolerance actions
under the Federal Food, Drug, and Cosmetic Act (FFDCA).
[[Page 2726]]
DATES: This regulation is effective January 19, 2022. Objections and
requests for hearings must be received on or before March 21, 2022, 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-2021-0045, is available at
https://www.regulations.gov or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket) in the Environmental Protection
Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg.,
Rm. 3334, 1301 Constitution Ave. NW, Washington, DC 20460-0001. The
Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805.
Due to the public health concerns relating to COVID-19, the EPA
Docket Center (EPA/DC) and Reading Room is closed to visitors with
limited exceptions. The staff continues to provide customer service via
email, phone, and webform. For the latest status information on EPA/DC
services, docket access, visit https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Marietta Echeverria, Acting Director,
Registration Division (7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington,
DC 20460-0001; main telephone number: (703) 305-7090; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other relatedinformation?
You may access a frequently updated electronic version of EPA's
tolerance regulations at 40 CFR part 180 through the Office of the
Federal Register's e-CFR site at https://www.ecfr.gov/current/title-40.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a(g), any person may file
an objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2021-0045 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
March 21, 2022. 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-2021-0045, 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/where-send-comments-epa-dockets.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of March 22, 2021 (86 FR 15162) (FRL-10021-
44) EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide petition (PP
0E8871) by IR-4, North Carolina State University, 1730 Varsity Drive,
Venture IV, Suite 210, Raleigh, NC 27606. The petition requested to
establish tolerances in 40 CFR 180.622 for residues of the fungicide
ethaboxam, (N-(cyano-2-thienylmethyl)-4-ethyl-2-(ethylamino)-5-
thiazolecarboxamide) in or on Brassica, leafy greens, subgroup 4-16B at
7 parts per million (ppm) and Vegetable, Brassica, head and stem, group
5-16 at 3 ppm. That document referenced a summary of the petition
prepared by IR-4, the petitioner, which is available in the docket,
https://www.regulations.gov. There were no comments received in
response to the notice of filing.
III. Aggregate Risk Assessment and Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a
tolerance (the legal limit for a pesticide chemical residue in or on a
food) only if EPA determines that the tolerance is ``safe.'' Section
408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a
reasonable certainty that no harm will result from aggregate exposure
to the pesticide chemical residue, including all anticipated dietary
exposures and all other exposures for which there is reliable
information.'' This includes exposure through drinking water and in
residential settings but does not include occupational exposure.
Section 408(b)(2)(C) of FFDCA requires EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance and to ``ensure that there
is a reasonable certainty that no harm will result to infants and
children from aggregate exposure to the pesticide chemical residue. . .
. ''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified therein, EPA has reviewed the available scientific data and
other relevant information in support of this action. EPA has
sufficient data to assess the hazards of and to make a determination on
aggregate exposure for ethaboxam including exposure resulting from the
tolerances established by this action. EPA's assessment of exposures
and risks associated with ethaboxam follows.
In an effort to streamline its publications in the Federal
Register,
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EPA is not reprinting sections that repeat what has been previously
published for tolerance rulemakings of the same pesticide chemical.
Where scientific information concerning a particular chemical remains
unchanged, the content of those sections would not vary between
tolerance rulemaking, and EPA considers referral back to those sections
as sufficient to provide an explanation of the information EPA
considered in making its safety determination for the new rulemaking.
EPA has previously published tolerance rulemakings for ethaboxam,
in which EPA concluded, based on the available information, that there
is a reasonable certainty that no harm would result from aggregate
exposure to ethaboxam and established tolerances for residues of that
chemical. EPA is incorporating previously published sections from those
rulemakings that remain unchanged as described further in this
rulemaking.
Toxicological profile. For a discussion of the Toxicological
Profile of ethaboxam, see Unit III.A. of the ethaboxam tolerance
rulemaking published in the Federal Register of August 3, 2017 (82 FR
36086) (FRL-9961-69).
Toxicological points of departure/Levels of concern. For a summary
of the Toxicological Points of Departure/Levels of Concern for
ethaboxam used for human risk assessment, see Unit III.B. of the August
3, 2017 ethaboxam tolerance rulemaking.
Exposure assessment. Much of the exposure assessment remains
unchanged from the previous rulemaking, although the exposure
assessment has been updated to include the petitioned-for tolerances
based on the same previous assumptions of tolerance level residues and
100 percent crop treated (PCT). Additionally, the estimated drinking
water concentration is the same as that used in the previous assessment
(7.4 ppb) for the chronic assessment (the only dietary assessment
needed). There are no residential uses for ethaboxam, therefore no
short- or intermediate-term exposure is expected. For a description of
the previous approach to and assumptions for the exposure assessment,
please reference Unit III.C. of the August 3, 2017 rulemaking.
Safety factor for infants and children. EPA continues to conclude
that there are reliable data to support the reduction of the Food
Quality Protection Act (FQPA) safety factor. See Unit III.D. of the
August 3, 2017 rulemaking for a discussion of the Agency's rationale
for that determination.
Aggregate risks and Determination of safety. EPA determines whether
acute and chronic dietary pesticide exposures are safe by comparing
aggregate exposure estimates to the acute population adjusted dose
(aPAD) and chronic population adjusted dose (cPAD). Short-,
intermediate-, and chronic risks are evaluated by comparing the
estimated aggregate food, water, and residential exposure to the
appropriate points of departure to ensure that an adequate margin of
exposure (MOE) exists. For linear cancer risks, EPA calculates the
lifetime probability of acquiring cancer given the estimated aggregate
exposure.
An acute endpoint attributable to a single dose exposure was not
identified; therefore, an acute dietary risk assessment was not
conducted. Chronic dietary risks are below the Agency's level of
concern of 100% of the cPAD; they are 39% of the cPAD for children 1 to
2 years old, the group with the highest estimated exposure. As the
chronic dietary endpoint and dose are protective of potential cancer
effects, ethaboxam is not expected to pose a dietary or aggregate
cancer risk of concern.
Therefore, based on the risk assessments and information described
above, EPA concludes there is a reasonable certainty that no harm will
result to the general population, or to infants and children, from
aggregate exposure to ethaboxam residues. More detailed information on
this action can be found in the document entitled, ``Ethaboxam. Human
Health Risk Assessment for the Proposed New Uses on Brassica Head and
Stem Vegetable Crop Group 5-16 and Brassica Leafy Greens Crop Subgroup
4-16B'' by going to the docket established by this action, EPA-HQ-OPP-
2021-0045.
IV. Other Considerations
A. Analytical Enforcement Methodology
For a discussion of the available analytical enforcement method,
see Unit IV.A. of the August 3, 2017 rulemaking.
B. International Residue Limits
In making its tolerance decisions, EPA seeks to harmonize U.S.
tolerances with international standards whenever possible, consistent
with U.S. food safety standards and agricultural practices. EPA
considers the international maximum residue limits (MRLs) established
by the Codex Alimentarius Commission (Codex), as required by FFDCA
section 408(b)(4).
Codex does not have established MRLs for ethaboxam in commodities
that are members of subgroup 4-16B or group 5-16.
V. Conclusion
Therefore, tolerances are established for residues of ethaboxam in
or on Brassica, leafy greens, subgroup 4-16B at 7 ppm and Vegetable,
Brassica, head and stem, group 5-16 at 3 ppm.
VI. Statutory and Executive Order Reviews
This action establishes tolerances under FFDCA section 408(d) in
response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001), or to Executive Order 13045,
entitled ``Protection of Children from Environmental Health Risks and
Safety Risks'' (62 FR 19885, April 23, 1997). This action does not
contain any information collections subject to OMB approval under the
Paperwork Reduction Act (PRA) (44 U.S.C. 3501 et seq.), nor does it
require any special considerations under Executive Order 12898,
entitled ``Federal Actions to Address Environmental Justice in Minority
Populations and Low-Income Populations'' (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerances in
this final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or Tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
Tribal Governments, on the relationship between the National Government
and the States or Tribal Governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian Tribes. Thus, the Agency has
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determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999) and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November 9, 2000) do not apply to this action. In addition, this
action does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
(UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides, and pests, Reporting and
recordkeeping requirements.
Dated: December 29, 2021.
Daniel Rosenblatt,
Acting Director, Registration Division, Office of Pesticide Programs.
Therefore, for the reasons stated in the preamble, EPA is amending
40 CFR chapter 1 as follows:
PART 180--TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES
IN FOOD
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. Amend Sec. 180.622, by adding in alphabetical order to table 1 to
paragraph (a) the entries ``Brassica, leafy greens, subgroup 4-16B''
and ``Vegetable, Brassica, head and stem, group 5-16'' to read as
follows:
Sec. 180.622 Ethaboxam; tolerances for residues.
(a) * * *
Table 1 to Paragraph (a)
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * *
Brassica, leafy greens, subgroup 4-16B....................... 7
* * * * *
Vegetable, Brassica, head and stem, group 5-16............... 3
* * * * *
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[FR Doc. 2022-00854 Filed 1-18-22; 8:45 am]
BILLING CODE 6560-50-P