Rimsulfuron; Pesticide Tolerances, 4732-4735 [2023-01131]
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Federal Register / Vol. 88, No. 16 / Wednesday, January 25, 2023 / Rules and Regulations
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
VIII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: January 13, 2023.
Daniel Rosenblatt,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, for the reasons stated in the
preamble, EPA is amending 40 CFR
chapter I as follows:
PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
CHEMICAL RESIDUES IN FOOD
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.920, amend Table 1 to
180.920 by adding, in alphabetical
order, an entry for ‘‘Malic acid (CAS
Reg. No. 6915–15–7)’’ to read as follows:
■
§ 180.920 Inert ingredients used preharvest; exemptions from the requirement
of a tolerance.
*
*
*
*
*
TABLE 1 TO 180.920
Inert ingredients
Limits
*
*
*
Malic acid (CAS Reg. No. 6915–15–7) ...................................
*
..............................
*
*
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[FR Doc. 2023–01155 Filed 1–24–23; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2021–0447; FRL–10478–01–
OCSPP]
Rimsulfuron; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
tolerances for residues of rimsulfuron in
or on pomegranate and tropical and
subtropical, small fruit, edible peel,
subgroup 23A. The Interregional
Research Project No. 4 (IR–4) requested
these tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective
January 25, 2023. Objections and
requests for hearings must be received
on or before March 27, 2023, 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–2021–0447, 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
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SUMMARY:
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Uses
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Buffering and stabilizing agent.
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Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room and the OPP
docket is (202) 566–1744. For the latest
status information on EPA/DC services,
docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Daniel Rosenblatt, Acting Director,
Registration Division (7505T), Office of
Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460–0001;
main telephone number: (202) 566–
1030; email address: RDFRNotices@
epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
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• Pesticide manufacturing (NAICS
code 32532).
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Office of the Federal Register’s eCFR 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, 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–2021–0447 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 27, 2023. Addresses for
mail and hand delivery of objections
and hearing requests are provided in 40
CFR 178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
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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–
2021–0447, by one of the following
methods:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
online instructions for submitting
comments. Do not submit electronically
any information you consider to be CBI
or other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW, Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
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II. Summary of Petitioned-For
Tolerance
In the Federal Register of September
22, 2021 (86 FR 52624) (FRL–8792–03–
OCSPP), 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 1E8926) by
IR–4, North Carolina State University,
1730 Varsity Drive, Venture IV, Suite
210, Raleigh, NC 27606. The petition
requested that 40 CFR 180.478 be
amended by establishing tolerances for
residues of the herbicide rimsulfuron
(N-[[(4,6-dimethoxy-2pyrimidinyl)amino]carbonyl]-3(ethylsulfonyl)-2-pyridinesulfonamide),
in or on pomegranate at 0.01 parts per
million (ppm) and tropical and
subtropical, small fruit, edible peel,
subgroup 23A at 0.01 ppm. There were
no comments received in response to
the notice of filing.
III. Aggregate Risk Assessment and
Determination of Safety
FFDCA section 408(b)(2)(A)(i) 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.’’ FFDCA
section 408(b)(2)(A)(ii) 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
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occupational exposure. FFDCA section
408(b)(2)(C) requires EPA to give special
consideration to exposure of infants and
children to the pesticide chemical
residue in establishing a tolerance and
to ‘‘ensure that there is a reasonable
certainty that no harm will result to
infants and children from aggregate
exposure to the pesticide chemical
residue . . . .’’
Consistent with FFDCA section
408(b)(2)(D), and the factors specified in
FFDCA section 408(b)(2)(D), EPA has
reviewed the available scientific data
and other relevant information in
support of this action. EPA has
sufficient data to assess the hazards of
and to make a determination on
aggregate exposure for rimsulfuron
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with rimsulfuron follows.
In an effort to streamline its
publications in the Federal Register,
EPA is not reprinting sections that
repeat what has been previously
published for tolerance rulemaking 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
republishing the same sections is
unnecessary. 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 a
tolerance rulemaking for rimsulfuron in
which EPA concluded, based on the
available information, that there is a
reasonable certainty that no harm would
result from aggregate exposure to
rimsulfuron and established tolerances
for residues of that chemical. EPA is
incorporating previously published
sections from this rulemaking as
described further in this rulemaking, as
they remain unchanged.
Toxicological profile. For a discussion
of the Toxicological Profile of
rimsulfuron, see Unit III.A of the
February 12, 2018, final rulemaking (83
FR 5942) (FRL–9972–36).
Points of departure/Levels of concern.
A summary of the toxicological
endpoints for rimsulfuron used for
human risk assessment is discussed in
Unit III.B of the February 12, 2018, final
rulemaking.
Exposure assessment. Much of the
exposure assessment remains the same
although updates have occurred to
accommodate the exposures from the
petitioned-for tolerances. These updates
are discussed in this section; for a
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description of the rest of the EPA
approach to and assumptions for the
exposure assessment, please reference
Unit III.C of the February 12, 2018, final
rulemaking.
EPA’s dietary exposure assessments
have been updated to include the
additional exposures from the new uses
of rimsulfuron on pomegranate and
tropical and subtropical, small fruit,
edible peel, subgroup 23A. An
unrefined chronic dietary (food and
drinking water) exposure and risk
assessment was conducted using the
Dietary Exposure Evaluation Model
software with the Food Commodity
Intake Database (DEEM–FCID) Version
4.02. This software incorporates 2005–
2010 consumption data from the U.S.
Department of Agriculture’s (USDA’s)
National Health and Nutrition
Examination Survey, What We Eat in
America (NHANES/WWEIA). The
chronic assessment used tolerance level
residues for all crops and assumed that
100% of the crops were treated with
rimsulfuron. The Agency’s default
processing factors were used where
available. An acute dietary exposure
assessment was not conducted since
there was no adverse effect observed for
a single dose of rimsulfuron.
Dietary exposure from drinking water.
The new uses do not result in an
increase in the estimated residue levels
in drinking water, so EPA used the same
estimated drinking water concentrations
in the chronic dietary assessment as
identified in Unit III.C of the February
12, 2018, rulemaking.
From non-dietary exposure. There are
no proposed residential uses at this
time; however, there are existing
residential uses on turf that have been
previously assessed using current data
and assumptions. For the residential
assessment of the turf uses, EPA did not
conduct a quantitative residential
handler risk assessment. The end use
label requires handlers to wear specific
clothing (long-sleeve shirt and long
pants) and chemical-resistant gloves, so
EPA assumed the product is not for
homeowner use. There is the potential
for post-application dermal exposures;
however, a residential post-application
dermal exposure assessment was not
conducted because no dermal hazard
was identified in the rimsulfuron
database. The quantifiable postapplication residential risk estimates
reflect incidental oral exposure to
children 1 to less than 2 years old from
hand-to-mouth exposure to turf treated
with rimsulfuron. The margin of
exposure (MOE) is 26,000, which is
greater than the level of concern of 100
and is not of concern.
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Cumulative effects from substances
with a common mechanism of toxicity.
In 2016, EPA’s Office of Pesticide
Programs released a guidance document
entitled, Pesticide Cumulative Risk
Assessment: Framework for Screening
Analysis https://www.epa.gov/pesticidescience-and-assessing-pesticide-risks/
pesticide-cumulative-risk-assessmentframework. The agency has utilized this
framework for rimsulfuron and
determined that although rimsulfuron
shares some chemical and/or
toxicological characteristics (e.g.,
chemical structure or apical endpoint)
with other pesticides, the toxicological
database does not support a testable
hypothesis for a common mechanism of
action. No further data are required to
determine that no common mechanism
of toxicity exists for rimsulfuron and
other pesticides and no further
cumulative evaluation is necessary for
rimsulfuron.
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 (SF) from 10X
to 1X for all risk scenarios. See Unit
III.D. of the February 12, 2018, final
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
the chronic population adjusted dose
(cPAD). Short-, intermediate-, and
chronic-term risks are evaluated by
comparing the estimated aggregate food,
water, and residential exposure to the
appropriate points of departure to
ensure that an adequate MOE exists. For
linear cancer risks, EPA calculates the
lifetime probability of acquiring cancer
given the estimated aggregate exposure.
An acute dietary exposure assessment
was not conducted since there was no
adverse effect observed for a single dose
of rimsulfuron. Chronic dietary risks are
below the Agency’s level of concern of
100% of the cPAD; they are 1.8% of the
cPAD for all infants (<1 year old), the
population group receiving the greatest
exposure.
The short-term aggregate exposure
assessment for children 1 to less than 2
years old includes dietary (food and
drinking water) and incidental oral
exposure from hand-to-mouth activities
from post-application exposure to turf.
The short-term aggregate risk estimate
for children 1 to less than 2 years old
is an MOE of 3,700, which is greater
than the level of concern of 100 and is
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not of concern. Acute risks are not
expected due to no adverse effect
observed for a single dose of
rimsulfuron; and chronic aggregate risks
to adults and children are equivalent to
the dietary (food and drinking water)
risks for those respective assessments
and are not of concern. Because there is
no intermediate-term residential
exposure and chronic dietary exposure
has already been assessed under the
appropriately protective cPAD, no
further assessment of intermediate-term
risk is necessary. Based on the lack of
evidence of carcinogenicity in two
adequate rodent carcinogenicity studies,
rimsulfuron is not expected to pose a
cancer risk to humans.
Therefore, based on the risk
assessments and information described
above, EPA concludes that there is a
reasonable certainty that no harm will
result to the general population, or to
infants and children from aggregate
exposure to rimsulfuron residues. More
detailed information on this action can
be found in the document
‘‘Rimsulfuron. Human Health Risk
Assessment in Support of a Petition for
the Establishment of Permanent
Tolerances on Pomegranate and
Tropical and Subtropical, Small Fruit,
Edible Peel, Subgroup 23A’’ in docket
ID No. EPA–HQ–OPP–2021–0447.
IV. Other Considerations
A. Analytical Enforcement Methodology
For a discussion of the available
analytical enforcement method for
various crops, see Unit IV.A of the
February 12, 2018, 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 has not established MRLs for
residues of rimsulfuron in or on any
commodity associated with this action.
V. Conclusion
Therefore, tolerances are established
for residues of rimsulfuron (N-[[(4,6dimethoxy-2pyrimidinyl)amino]carbonyl]-3(ethylsulfonyl)-2-pyridinesulfonamide),
in or on pomegranate at 0.01 ppm and
tropical and subtropical, small fruit,
edible peel, subgroup 23A at 0.01 ppm.
In addition, as a housekeeping
measure, EPA is removing the tolerance
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for potato at 0.1 ppm, which expired on
August 12, 2018, and has no effect at
this time.
VI. Statutory and Executive Order
Reviews
This action establishes tolerances
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997). This action does not
contain any information collections
subject to OMB approval under the
Paperwork Reduction Act (PRA) (44
U.S.C. 3501 et seq.), nor does it require
any special considerations under
Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerances in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or Tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
has determined that this action will not
have a substantial direct effect on States
or Tribal Governments, on the
relationship between the National
Government and the States or Tribal
Governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
Tribes. Thus, the Agency has
determined that Executive Order 13132,
entitled ‘‘Federalism’’ (64 FR 43255,
August 10, 1999) and Executive Order
13175, entitled ‘‘Consultation and
Coordination with Indian Tribal
Governments’’ (65 FR 67249, November
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Federal Register / Vol. 88, No. 16 / Wednesday, January 25, 2023 / Rules and Regulations
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 (CRA)
Pursuant to the CRA (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
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.
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: January 13, 2023.
Daniel Rosenblatt,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, for the reasons stated in the
preamble, EPA is amending 40 CFR
chapter I as follows:
2. In § 180.478, in paragraph (a)
amend table 1 by:
■ a. Adding in alphabetical order the
entry ‘‘Pomegranate’’;
■ b. Removing the entry for ‘‘Potato’’
and the footnote; and
■ c. Adding in alphabetical order the
entry ‘‘Tropical and subtropical, small
fruit, edible peel, subgroup 23A’’.
The additions read as follows:
■
§ 180.478
residues
Rimsulfuron; tolerances for
(a) * * *
TABLE 1 TO PARAGRAPH (a)
Parts per
million
Commodity
*
*
*
*
*
*
Pomegranate .......................................................................................................................................................................................
*
*
*
*
*
*
*
Tropical and subtropical, small fruit, edible peel, subgroup 23A ........................................................................................................
*
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*
*
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[FR Doc. 2023–01131 Filed 1–24–23; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
42 CFR Part 68
[Docket Number—NIH–2020–0001]
RIN 0925–AA68
National Institutes of Health Loan
Repayment Programs
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Final rule.
The Department of Health and
Human Services (HHS or Department),
through the National Institutes of Health
(NIH), is updating the existing
regulation for NIH Loan Repayment
Programs (LRPs) to reflect the
consolidation of NIH LRPs into two
programs, the Intramural Loan
Repayment Program (for NIH
researchers) and the Extramural Loan
Repayment Program (for non-NIH
researchers); the direct authority of the
NIH Director to administer the NIH
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LRPs (formerly the duty of the
Secretary, HHS); and the increase in the
annual loan repayment amount from a
maximum of $35,000 to a maximum of
$50,000.
DATES: This final rule is effective
February 24, 2023.
FOR FURTHER INFORMATION CONTACT:
Daniel Hernandez, NIH Regulations
Officer, Office of Management
Assessment, NIH, Rockledge 1, 6705
Rockledge Drive, Suite 601, Room 601–
T, Bethesda, MD 20817, MSC 7901, by
email at dhernandez@mail.nih.gov, or
by telephone at 301–435–3343 (not a
toll-free number). For program
information contact: Matthew Lockhart,
NIH Division of Loan Repayment, by
email matthew.lockhart@nih.gov, or
telephone 866–849–4047. Information
regarding the requirements, application
deadline dates, and an on-line
application for the NIH Loan Repayment
Programs may be obtained from the NIH
Loan Repayment Program website
https://www.lrp.nih.gov/.
SUPPLEMENTARY INFORMATION:
I. Background and Statutory Authority
The purpose of the NIH LRP programs
is to recruit and retain highly qualified
health professionals as biomedical and
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0.01
0.01
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behavioral researchers. The programs
offer educational loan repayment for
participants who agree, by written
contract, to engage in qualifying
domestic non-profit supported research
at a qualifying non-NIH institution, or as
an NIH employee for a minimum of two
years (or three years for the Intramural
LRP’s general research subcategory).
On December 13, 2016, Congress
enacted the 21st Century Cures Act,
Public Law (Pub. L.) 114–255, Section
2022 of which amended the Public
Health Service (PHS) Act to authorize
the consolidation of National Institutes
of Health Loan Repayment Programs
(LRPs) into the Intramural Loan
Repayment Program and the Extramural
Loan Repayment Program.
The legislation also provides the NIH
Director with the authority to establish
or eliminate one or more subcategories
of the LRPs to reflect workforce or
scientific needs related to biomedical
research. Thus, this statute allows for up
to four subcategories for the Intramural
Loan Repayment Program (General,
Acquired Immunodeficiency Syndrome
(AIDS), Clinical for Researchers from
Disadvantaged Backgrounds, and one
additional subcategory) and up to six
subcategories for the Extramural Loan
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Agencies
[Federal Register Volume 88, Number 16 (Wednesday, January 25, 2023)]
[Rules and Regulations]
[Pages 4732-4735]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-01131]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2021-0447; FRL-10478-01-OCSPP]
Rimsulfuron; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes tolerances for residues of
rimsulfuron in or on pomegranate and tropical and subtropical, small
fruit, edible peel, subgroup 23A. The Interregional Research Project
No. 4 (IR-4) requested these tolerances under the Federal Food, Drug,
and Cosmetic Act (FFDCA).
DATES: This regulation is effective January 25, 2023. Objections and
requests for hearings must be received on or before March 27, 2023, 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-2021-0447, 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 and the OPP docket is (202) 566-1744. For the latest
status information on EPA/DC services, docket access, visit https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Daniel Rosenblatt, Acting Director,
Registration Division (7505T), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington,
DC 20460-0001; main telephone number: (202) 566-1030; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of EPA's
tolerance regulations at 40 CFR part 180 through the Office of the
Federal Register's e-CFR site at https://www.ecfr.gov/current/title-40.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, any person may file an
objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2021-0447 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 27, 2023. Addresses for mail and hand delivery of objections and
hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be
[[Page 4733]]
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-2021-0447, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be CBI or other
information whose disclosure is restricted by statute.
Mail: OPP Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW, Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of September 22, 2021 (86 FR 52624) (FRL-
8792-03-OCSPP), 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 1E8926) by IR-4, North Carolina State University, 1730
Varsity Drive, Venture IV, Suite 210, Raleigh, NC 27606. The petition
requested that 40 CFR 180.478 be amended by establishing tolerances for
residues of the herbicide rimsulfuron (N-[[(4,6-dimethoxy-2-
pyrimidinyl)amino]carbonyl]-3-(ethylsulfonyl)-2-pyridinesulfonamide),
in or on pomegranate at 0.01 parts per million (ppm) and tropical and
subtropical, small fruit, edible peel, subgroup 23A at 0.01 ppm. There
were no comments received in response to the notice of filing.
III. Aggregate Risk Assessment and Determination of Safety
FFDCA section 408(b)(2)(A)(i) 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.'' FFDCA section
408(b)(2)(A)(ii) 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. FFDCA section 408(b)(2)(C)
requires EPA to give special consideration to exposure of infants and
children to the pesticide chemical residue in establishing a tolerance
and to ``ensure that there is a reasonable certainty that no harm will
result to infants and children from aggregate exposure to the pesticide
chemical residue . . . .''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified in FFDCA section 408(b)(2)(D), EPA has reviewed the available
scientific data and other relevant information in support of this
action. EPA has sufficient data to assess the hazards of and to make a
determination on aggregate exposure for rimsulfuron including exposure
resulting from the tolerances established by this action. EPA's
assessment of exposures and risks associated with rimsulfuron follows.
In an effort to streamline its publications in the Federal
Register, EPA is not reprinting sections that repeat what has been
previously published for tolerance rulemaking 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 republishing the same sections is unnecessary.
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 a tolerance rulemaking for rimsulfuron
in which EPA concluded, based on the available information, that there
is a reasonable certainty that no harm would result from aggregate
exposure to rimsulfuron and established tolerances for residues of that
chemical. EPA is incorporating previously published sections from this
rulemaking as described further in this rulemaking, as they remain
unchanged.
Toxicological profile. For a discussion of the Toxicological
Profile of rimsulfuron, see Unit III.A of the February 12, 2018, final
rulemaking (83 FR 5942) (FRL-9972-36).
Points of departure/Levels of concern. A summary of the
toxicological endpoints for rimsulfuron used for human risk assessment
is discussed in Unit III.B of the February 12, 2018, final rulemaking.
Exposure assessment. Much of the exposure assessment remains the
same although updates have occurred to accommodate the exposures from
the petitioned-for tolerances. These updates are discussed in this
section; for a description of the rest of the EPA approach to and
assumptions for the exposure assessment, please reference Unit III.C of
the February 12, 2018, final rulemaking.
EPA's dietary exposure assessments have been updated to include the
additional exposures from the new uses of rimsulfuron on pomegranate
and tropical and subtropical, small fruit, edible peel, subgroup 23A.
An unrefined chronic dietary (food and drinking water) exposure and
risk assessment was conducted using the Dietary Exposure Evaluation
Model software with the Food Commodity Intake Database (DEEM-FCID)
Version 4.02. This software incorporates 2005-2010 consumption data
from the U.S. Department of Agriculture's (USDA's) National Health and
Nutrition Examination Survey, What We Eat in America (NHANES/WWEIA).
The chronic assessment used tolerance level residues for all crops and
assumed that 100% of the crops were treated with rimsulfuron. The
Agency's default processing factors were used where available. An acute
dietary exposure assessment was not conducted since there was no
adverse effect observed for a single dose of rimsulfuron.
Dietary exposure from drinking water. The new uses do not result in
an increase in the estimated residue levels in drinking water, so EPA
used the same estimated drinking water concentrations in the chronic
dietary assessment as identified in Unit III.C of the February 12,
2018, rulemaking.
From non-dietary exposure. There are no proposed residential uses
at this time; however, there are existing residential uses on turf that
have been previously assessed using current data and assumptions. For
the residential assessment of the turf uses, EPA did not conduct a
quantitative residential handler risk assessment. The end use label
requires handlers to wear specific clothing (long-sleeve shirt and long
pants) and chemical-resistant gloves, so EPA assumed the product is not
for homeowner use. There is the potential for post-application dermal
exposures; however, a residential post-application dermal exposure
assessment was not conducted because no dermal hazard was identified in
the rimsulfuron database. The quantifiable post-application residential
risk estimates reflect incidental oral exposure to children 1 to less
than 2 years old from hand-to-mouth exposure to turf treated with
rimsulfuron. The margin of exposure (MOE) is 26,000, which is greater
than the level of concern of 100 and is not of concern.
[[Page 4734]]
Cumulative effects from substances with a common mechanism of
toxicity. In 2016, EPA's Office of Pesticide Programs released a
guidance document entitled, Pesticide Cumulative Risk Assessment:
Framework for Screening Analysis https://www.epa.gov/pesticide-science-and-assessing-pesticide-risks/pesticide-cumulative-risk-assessment-framework. The agency has utilized this framework for rimsulfuron and
determined that although rimsulfuron shares some chemical and/or
toxicological characteristics (e.g., chemical structure or apical
endpoint) with other pesticides, the toxicological database does not
support a testable hypothesis for a common mechanism of action. No
further data are required to determine that no common mechanism of
toxicity exists for rimsulfuron and other pesticides and no further
cumulative evaluation is necessary for rimsulfuron.
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 (SF) from 10X to 1X for all
risk scenarios. See Unit III.D. of the February 12, 2018, final
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 the chronic population adjusted dose (cPAD). Short-,
intermediate-, and chronic-term risks are evaluated by comparing the
estimated aggregate food, water, and residential exposure to the
appropriate points of departure to ensure that an adequate MOE exists.
For linear cancer risks, EPA calculates the lifetime probability of
acquiring cancer given the estimated aggregate exposure.
An acute dietary exposure assessment was not conducted since there
was no adverse effect observed for a single dose of rimsulfuron.
Chronic dietary risks are below the Agency's level of concern of 100%
of the cPAD; they are 1.8% of the cPAD for all infants (<1 year old),
the population group receiving the greatest exposure.
The short-term aggregate exposure assessment for children 1 to less
than 2 years old includes dietary (food and drinking water) and
incidental oral exposure from hand-to-mouth activities from post-
application exposure to turf. The short-term aggregate risk estimate
for children 1 to less than 2 years old is an MOE of 3,700, which is
greater than the level of concern of 100 and is not of concern. Acute
risks are not expected due to no adverse effect observed for a single
dose of rimsulfuron; and chronic aggregate risks to adults and children
are equivalent to the dietary (food and drinking water) risks for those
respective assessments and are not of concern. Because there is no
intermediate-term residential exposure and chronic dietary exposure has
already been assessed under the appropriately protective cPAD, no
further assessment of intermediate-term risk is necessary. Based on the
lack of evidence of carcinogenicity in two adequate rodent
carcinogenicity studies, rimsulfuron is not expected to pose a cancer
risk to humans.
Therefore, based on the risk assessments and information described
above, EPA concludes that there is a reasonable certainty that no harm
will result to the general population, or to infants and children from
aggregate exposure to rimsulfuron residues. More detailed information
on this action can be found in the document ``Rimsulfuron. Human Health
Risk Assessment in Support of a Petition for the Establishment of
Permanent Tolerances on Pomegranate and Tropical and Subtropical, Small
Fruit, Edible Peel, Subgroup 23A'' in docket ID No. EPA-HQ-OPP-2021-
0447.
IV. Other Considerations
A. Analytical Enforcement Methodology
For a discussion of the available analytical enforcement method for
various crops, see Unit IV.A of the February 12, 2018, 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 has not established MRLs for residues of
rimsulfuron in or on any commodity associated with this action.
V. Conclusion
Therefore, tolerances are established for residues of rimsulfuron
(N-[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]-3-(ethylsulfonyl)-2-
pyridinesulfonamide), in or on pomegranate at 0.01 ppm and tropical and
subtropical, small fruit, edible peel, subgroup 23A at 0.01 ppm.
In addition, as a housekeeping measure, EPA is removing the
tolerance for potato at 0.1 ppm, which expired on August 12, 2018, and
has no effect at this time.
VI. Statutory and Executive Order Reviews
This action establishes tolerances under FFDCA section 408(d) in
response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001) or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997). This action does not contain any
information collections subject to OMB approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et seq.), nor does it require any
special considerations under Executive Order 12898, entitled ``Federal
Actions to Address Environmental Justice in Minority Populations and
Low-Income Populations'' (59 FR 7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerances in
this final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or Tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
Tribal Governments, on the relationship between the National Government
and the States or Tribal Governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian Tribes. Thus, the Agency has
determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999) and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November
[[Page 4735]]
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 (CRA)
Pursuant to the CRA (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: January 13, 2023.
Daniel Rosenblatt,
Acting Director, Registration Division, Office of Pesticide Programs.
Therefore, for the reasons stated in the preamble, EPA is amending
40 CFR chapter I as follows:
PART 180--TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES
IN FOOD
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. In Sec. 180.478, in paragraph (a) amend table 1 by:
0
a. Adding in alphabetical order the entry ``Pomegranate'';
0
b. Removing the entry for ``Potato'' and the footnote; and
0
c. Adding in alphabetical order the entry ``Tropical and subtropical,
small fruit, edible peel, subgroup 23A''.
The additions read as follows:
Sec. 180.478 Rimsulfuron; tolerances for residues
(a) * * *
Table 1 to Paragraph (a)
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * * * *
Pomegranate............................................. 0.01
* * * * * * *
Tropical and subtropical, small fruit, edible peel, 0.01
subgroup 23A...........................................
* * * * * * *
------------------------------------------------------------------------
* * * * *
[FR Doc. 2023-01131 Filed 1-24-23; 8:45 am]
BILLING CODE 6560-50-P