O-Benzyl-P-Chlorophenol (OBPCP); Exemption From the Requirement of a Pesticide Tolerance, 6016-6019 [2024-01869]
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Federal Register / Vol. 89, No. 21 / Wednesday, January 31, 2024 / Rules and Regulations
§ 356.8 Continued suspension of
liquidation.
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(2) A participant in a binational panel
review that was a domestic party to the
proceeding, as described in section
771(9)(C), (D), (E), (F), or (G) of the Act
(19 U.S.C. 1677(9)(C), (D), (E), (F) and
(G)), may request continued suspension
of liquidation of entries of merchandise
covered by the administrative
determination under review by the
panel and that would be affected by the
panel review. Foreign governments are
not listed as interested parties who may
request the continuation of suspension
under 19 U.S.C. 1516a(g)(5)(C)(iii).
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■ 4. In § 356.9, revise paragraph (g) to
read as follows:
§ 356.9 Persons authorized to receive
proprietary information
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(g) Every court report, interpreter, and
translator employed in a panel or
extraordinary challenge committee
review, as well as individuals employed
to provide audiovisual services at
hearings, meetings, or other events as
needed.
[FR Doc. 2024–01475 Filed 1–30–24; 8:45 am]
BILLING CODE 3510–DS–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2023–0225; FRL–10919–02–
OCSPP]
O-Benzyl-P-Chlorophenol (OBPCP);
Exemption From the Requirement of a
Pesticide Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
exemptions from the requirement of a
tolerance for residues of ortho-benzylpara-chlorophenol, potassium 2-benzyl4-chlorophenate, and sodium 2-benzyl4-chlorophenate on food contact
surfaces when applied/used in public
eating places, dairy processing
equipment, and/or food processing
equipment and utensils. These tolerance
exemptions are established on the
Agency’s own initiative under the
Federal Food, Drug, and Cosmetic Act
(FFDCA), in order to implement the
tolerance actions EPA identified during
its review of these chemicals as part of
the Agency’s registration review
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SUMMARY:
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program under the Federal Insecticide,
Fungicide, and Rodenticide Act
(FIFRA).
This regulation is effective
January 31, 2024. Objections and
requests for hearings must be received
on or before April 1, 2024, and must be
filed in accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
DATES:
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2023–0225, 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. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Anita Pease, Antimicrobials Division
(7510M), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; main telephone number:
(202) 566–0736; email address:
ADFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
I. General Information
A. Does this action apply to me?
You may be potentially affected by
this action if you are a 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 40 CFR part 180
through the Office of the Federal
Register’s e-CFR site at https://
www.ecfr.gov/current/title-40.
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C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2023–0255 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 in the Office of the
Administrative Law Judges on or before
April 1, 2024. Notwithstanding the
procedural requirements of 40 CFR
178.25(b), the Office of the
Administrative Law Judges has issued
an order urging parties to file and serve
documents with the Tribunal by
electronic means only. See Revised
Order Urging Electronic Filing and
Service (dated June 22, 2023), https://
www.epa.gov/system/files/documents/
2023-06/2023-06-22%20-%20revised
%20order%20urging%20electronic
%20filing%20and%20service.pdf.
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–
2023–0225, 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.
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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Federal Register / Vol. 89, No. 21 / Wednesday, January 31, 2024 / Rules and Regulations
II. Background
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A. Proposed Rule
In the Federal Register of May 5, 2023
(88 FR 29010) (FRL–10919–01–OCSPP),
EPA proposed to establish exemptions
from the requirement of a tolerance for
residues of the antimicrobial pesticides
ortho-benzyl-para-chlorophenol,
potassium 2-benzyl-4-chlorophenate,
and sodium 2-benzyl-4-chlorophenate
in food resulting from application to
food-contact surfaces in public eating
places, dairy-processing equipment, and
food-processing equipment and utensils.
The Agency had identified the need for
the exemptions as part of the
registration review process under the
Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA), 7 U.S.C.
136a(g), and published a proposed
rulemaking under its authority to
initiate tolerance rulemakings under the
FFDCA section 408(e), 21 U.S.C.
346a(e). That proposal noted that the
new exemptions would supersede the
current exemption for ortho-benzylpara-chlorophenol under 40 CFR
180.940(c) (listed as phenol, 4-chloro-2(phenylmethyl)-, an alternative name for
ortho-benzyl-para-chlorophenol), which
would be removed from the regulations
as unnecessary and redundant.
As noted in the proposal, the OBenzyl-p-Chlorophenol (OBPCP)
Interim Registration Review Decision
(OBPCP ID) identified the need for these
exemptions based on existing registered
pesticide uses, and the underlying risk
assessment concluded that there were
no risks of concern associated with
these uses. Consequently, EPA
concluded that the exemptions from the
requirement of a tolerance for residues
of ortho-benzyl-para-chlorophenol,
sodium 2-benzyl-4-chlorophenate, and
potassium 2-benzyl-4-chlorophenate,
when used in antimicrobial
formulations applied to food contact
surfaces in public eating places, dairy
processing equipment, and food
processing equipment and utensils
when used at concentrations not to
exceed 2,080 ppm in end-use
formulations, would be safe. Electronic
copies of the OBPCP ID and other
documents are available in EPA docket
number EPA–HQ–OPP–2011–0423,
which can be found at https://
www.regulations.gov.
B. What is the Agency’s authority for
taking this action?
Under section 408(e) of the FFDCA,
EPA can establish an exemption from
the requirement of a tolerance for
residues of a pesticide chemical after
publishing a proposed rule and
providing 60-day period for public
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comment. 21 U.S.C. 346a(e). EPA
published the proposed rule on May 5,
2023, and provided 60 days for public
comment (until July 5, 2023).
III. Final Rule
A. Comments
No substantive comments were
submitted in response to the proposed
rule.
B. Determination of Safety
Section 408(c)(2)(A)(i) of FFDCA
allows EPA to establish an exemption
from the requirement for a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the exemption is ‘‘safe.’’
Section 408(c)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings but does not include
occupational exposure. Pursuant to
FFDCA section 408(c)(2)(B), in
establishing or maintaining in effect an
exemption from the requirement of a
tolerance, EPA must take into account
the factors set forth in FFDCA section
408(b)(2)(C), which 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 . . . .’’
As noted in the proposed rule, EPA
reviewed the available scientific data
and other relevant information as part of
registration review and in support of
this action. Based on that review, EPA’s
proposed rule concluded that the
exemptions would be safe.
Since no comments were filed, EPA’s
assessment of the potential for risks
from exposure to these pesticide
chemicals and conclusions about the
safety of these exemptions remains
unchanged. Therefore, based on the lack
of any aggregate risks of concern, EPA
concludes that these exemptions from
the requirement of a tolerance for
residues of ortho-benzyl-parachlorophenol, sodium 2-benzyl-4chlorophenate, and potassium 2-benzyl4-chlorophenate, including the
limitation for the end-use formulation
concentration of each of these pesticides
to not exceed 2,080 ppm, are safe, i.e.,
there is a reasonable certainty that no
harm will result from aggregate
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exposures to ortho-benzyl-parachlorophenol, sodium 2-benzyl-4chlorophenate, or potassium 2-benzyl-4chlorophenate, when used in
accordance with the terms of the
respective exemptions. In addition, EPA
has determined that there is a
reasonable certainty that no harm will
result to infants and children from
aggregate exposure to the pesticide
chemical residues, in accordance with
FFDCA section 408(b)(2)(C).
IV. Conclusion
Therefore, exemptions from the
requirement of a tolerance are
established for residues of ortho-benzylpara-chlorophenol, potassium 2-benzyl4-chlorophenate, and sodium 2-benzyl4-chlorophenate, when used on or
applied to food contact surfaces in
public eating places, dairy processing
equipment, and food processing
equipment and utensils, with a
limitation in concentration of 2,080
ppm in end-use formulations. In
addition, EPA is removing the existing
exemption in 40 CFR 180.940(c) for
residues of phenol, 4-chloro-2(phenylmethyl)-, as it is unnecessary
and redundant upon the establishment
of these new exemptions.
V. Statutory and Executive Order
Reviews
Additional information about these
statutes and Executive orders can be
found at https://www.epa.gov/lawsregulations/laws-and-executiveorders#influence.
A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulations
and Regulatory Review
This action is exempt from review by
the Office of Management and Budget
(OMB) under Executive Orders 12866
(58 FR 51735, October 4, 1993) and
13563 (76 FR 3821, January 21, 2011)
because it establishes tolerance
exemptions under FFDCA section 408.
B. Paperwork Reduction Act (PRA)
This action does not impose an
information collection burden under the
PRA, 44 U.S.C. 3501 et seq., because it
does not contain any information
collection activities.
C. Regulatory Flexibility Act (RFA)
I certify that this action will not have
a significant economic impact on a
substantial number of small entities
under the RFA, 5 U.S.C. 601 et seq. In
making this determination, EPA
concludes that the impact of concern for
this rule is any significant adverse
economic impact on small entities and
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Federal Register / Vol. 89, No. 21 / Wednesday, January 31, 2024 / Rules and Regulations
that the Agency is certifying that this
rule will not have a significant
economic impact on a substantial
number of small entities because the
rule has no net burden on small entities
subject to the rule. As discussed in the
proposed rule, this takes into account
the EPA analysis for the establishment
and modification of tolerances.
Furthermore, the Agency did not receive
any comments on these conclusions as
presented in the proposed rule.
D. Unfunded Mandates Reform Act
(UMRA)
This action does not contain any
unfunded mandate as described in
UMRA, 2 U.S.C. 1531–1538, and does
not significantly or uniquely affect small
governments. The action imposes no
enforceable duty on any state, local, or
tribal governments or the private sector.
E. Executive Order 13132: Federalism
This action does not have federalism
implications as specified in Executive
Order 13132, August 10, 1999 (64 FR
43255). It will not have substantial
direct effects on the states, on the
relationship between the National
Government and the states, or on the
distribution of power and
responsibilities among the various
levels of government.
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F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
This action does not have tribal
implications as specified in Executive
Order 13175, November 9, 2000 (65 FR
67249), because it will not have
substantial direct effects on tribal
governments, on the relationship
between the Federal Government and
the Indian tribes, or on the distribution
of power and responsibilities between
the Federal Government and Indian
tribes.
G. Executive Order 13045: Protection of
Children From Environmental Health
Risks and Safety Risks
Executive Order 13045 (62 FR 19885,
April 23, 1997) directs Federal agencies
to include an evaluation of health and
safety effects of the planned regulation
on children in Federal health and safety
standards and explain why the
regulation is preferable to potential
effective and reasonably feasible
alternatives. This action is also not
subject to Executive Order 13045
because it is not a significant regulatory
action under section 3(f)(1) of Executive
Order 12866 (See Unit V.A.) and
because EPA does not believe the
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environmental health or safety risks
addressed by this action present a
disproportionate risk to children.
However, EPA’s Policy on Children’s
Health applies to this action.
This rule finalizes tolerance actions
under the FFDCA, which 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 . . .’’
(FFDCA 408(b)(2)(C)). Consistent with
FFDCA section 408(b)(2)(D), and the
factors specified therein, EPA has
reviewed the available scientific and
other data and other relevant
information in support of these final
tolerance actions. The Agency’s
consideration is documented in the
pesticide specific registration review
decision documents. See the discussion
in Unit III. and access the chemical
specific registration review documents
in each chemical docket at https://
www.regulations.gov.
considered the safety risks for the
pesticides subject to this rulemaking
and in the context of the tolerance
actions set out in this rulemaking. EPA
believes that the human health and
environmental conditions that exist
prior to this action do not result in
disproportionate and adverse effects on
people of color, low-income
populations, and/or indigenous peoples.
Furthermore, EPA believes that this
action is not likely to result in new
disproportionate and adverse effects on
people of color, low-income
populations, and/or indigenous peoples.
K. Congressional Review Act (CRA)
This action is subject to the CRA, 5
U.S.C. 801 et seq., and EPA will submit
a rule report to each House of the
Congress and to the Comptroller General
of the United States. 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.
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution or Use
This action is not a subject to
Executive Order 13211 (66 FR 28355,
May 22, 2001) because it is not a
significant regulatory action under
Executive Order 12866.
Dated: January 25, 2024.
Anita Pease,
Director, Antimicrobials Division, Office of
Pesticide Programs.
I. National Technology Transfer
Advancement Act (NTTAA)
This action does not involve technical
standards under NTTAA section 12(d),
15 U.S.C. 272.
PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
CHEMICAL RESIDUES IN FOOD
J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
Executive Order 12898 (59 FR 7629,
February 16, 1994) directs Federal
agencies, to the greatest extent
practicable and permitted by law, to
make environmental justice part of their
mission by identifying and addressing,
as appropriate, disproportionately high
and adverse human health or
environmental effects of their programs,
policies, and activities on minority
populations (people of color and/or
indigenous peoples) and low-income
populations. As discussed in more
detail in the pesticide specific risk
assessments conducted as part of the
registration review for the pesticides
identified in Unit II., EPA has
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Therefore, for the reasons stated in the
preamble, EPA amends 40 CFR chapter
I as follows:
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Amend § 180.940 by:
a. Adding in alphabetical order the
entries ‘‘Ortho-benzyl-parachlorophenol’’, ‘‘Potassium 2-benzyl-4chlorophenate’’, and ‘‘Sodium 2-benzyl4-chlorophenate’’ to table 1 to paragraph
(a).
■ b. Removing the entry ‘‘Phenol, 4chloro-2-(phenylmethyl)-’’ from the
table in paragraph (c).
The additions read as follows:
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§ 180.940 Tolerance exemptions for active
and inert ingredients for use in
antimicrobial formulations (Food-contact
surface sanitizing solutions).
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Federal Register / Vol. 89, No. 21 / Wednesday, January 31, 2024 / Rules and Regulations
TABLE 1 TO PARAGRAPH (a)
Pesticide chemical
CAS reg. No.
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Ortho-benzyl-para-chlorophenol ...................................
120–32–1
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Potassium 2-benzyl-4-chlorophenate ...........................
35471–49–9
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Sodium 2-benzyl-4-chlorophenate ................................
3184–65–4
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[FR Doc. 2024–01869 Filed 1–30–24; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Parts 409, 410, 414, 424, 484,
488, and 489
[CMS–1780–CN]
RIN 0938–AV03
Medicare Program; Calendar Year (CY)
2024 Home Health (HH) Prospective
Payment System Rate Update; HH
Quality Reporting Program
Requirements; HH Value-Based
Purchasing Expanded Model
Requirements; Home Intravenous
Immune Globulin Items and Services;
Hospice Informal Dispute Resolution
and Special Focus Program
Requirements, Certain Requirements
for Durable Medical Equipment
Prosthetics and Orthotics Supplies;
and Provider and Supplier Enrollment
Requirements; Correction
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
ACTION: Final rule; correction.
AGENCY:
This document corrects
technical errors in the final rule that
appeared in the November 13, 2023
Federal Register titled ‘‘Medicare
Program; Calendar Year (CY) 2024
Home Health (HH) Prospective Payment
System Rate Update; HH Quality
Reporting Program Requirements; HH
Value-Based Purchasing Expanded
Model Requirements; Home Intravenous
Immune Globulin Items and Services;
Hospice Informal Dispute Resolution
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SUMMARY:
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Limits
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When ready for use, the end-use concentration is not to exceed 2080
ppm.
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When ready for use, the end-use concentration is not to exceed 2080
ppm.
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When ready for use, the end-use concentration is not to exceed 2080
ppm.
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and Special Focus Program
Requirements, Certain Requirements for
Durable Medical Equipment Prosthetics
and Orthotics Supplies; and Provider
and Supplier Enrollment Requirements’’
(referred to hereafter as the ‘‘CY 2024
HH PPS final rule’’).
DATES: Effective date: This correcting
document is effective January 31, 2024.
FOR FURTHER INFORMATION CONTACT: For
questions about the Home Health
Quality Reporting Program (HH QRP),
send your inquiry via email to
HHQRPquestions@cms.hhs.gov.
For questions about the expanded
Home Health Value-Based Purchasing
Model, please visit the Expanded
HHVBP Model web page at https://
innovation.cms.gov/innovation-models/
expanded-home-health-value-basedpurchasing-model; send your inquiry
via email to HHVBPquestions@
cms.hhs.gov; or call Marcie O’Reilly at
(410) 786–9764.
For questions about the hospice
informal dispute resolution send
inquiries to QSOG_Hospice@
cms.hhs.gov, and for the special focus
program, send your inquiry to CMS_
HospiceSFP@cms.hhs.gov, or call
Thomas Pryor at (410) 786–1332.
SUPPLEMENTARY INFORMATION:
I. Background
This correcting document identifies
and corrects errors in FR Doc. 2023–
24455 of November 13, 2023 (88 FR
77676). The corrections in this
correcting document are effective
January 1, 2024, as if they had been
included in the document that appeared
in the November 13, 2023, Federal
Register.
II. Summary of Errors
On pages 77680, 77761, 77767, and
77851 in our discussion of the Home
Health Quality Reporting Program (HH
QRP), we made several typographical
errors.
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On pages 77778 and 77779, in a table
regarding the proposed measures for the
Home Health Value-Based Purchasing
Model (HHVBP), we made
typographical and technical errors.
On pages 77801, 77802, and 77807, in
our discussion of the Hospice Informal
Dispute Resolution and Special Focus
Program, we made several typographical
and technical errors.
We are correcting these errors in
section IV. of this correcting document.
III. Waiver of Proposed Rulemaking
and Delay in Effective Date
Under 5 U.S.C. 553(b) of the
Administrative Procedure Act (APA),
the agency is required to publish a
notice of the proposed rulemaking in
the Federal Register before the
provisions of a rule take effect.
Similarly, section 1871(b)(1) of the
Social Security Act (the Act) requires
the Secretary to provide for notice of the
proposed rulemaking in the Federal
Register and provide a period of not less
than 60 days for public comment. In
addition, section 553(d) of the APA, and
section 1871(e)(1)(B)(i) of the Act
mandate a 30-day delay in effective date
after issuance or publication of a rule.
Sections 553(b)(B) and 553(d)(3) of the
APA provide for exceptions from the
notice and comment and delay in
effective date APA requirements; in
cases in which these exceptions apply,
sections 1871(b)(2)(C) and
1871(e)(1)(B)(ii) of the Act provide
exceptions from the notice and 60-day
comment period and delay in effective
date requirements of the Act as well.
Section 553(b)(B) of the APA and
section 1871(b)(2)(C) of the Act
authorize an agency to dispense with
normal rulemaking requirements for
good cause if the agency makes a
finding that the notice and comment
process are impracticable, unnecessary,
or contrary to the public interest. In
addition, both section 553(d)(3) of the
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Agencies
[Federal Register Volume 89, Number 21 (Wednesday, January 31, 2024)]
[Rules and Regulations]
[Pages 6016-6019]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-01869]
=======================================================================
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2023-0225; FRL-10919-02-OCSPP]
O-Benzyl-P-Chlorophenol (OBPCP); Exemption From the Requirement
of a Pesticide Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes exemptions from the requirement of
a tolerance for residues of ortho-benzyl-para-chlorophenol, potassium
2-benzyl-4-chlorophenate, and sodium 2-benzyl-4-chlorophenate on food
contact surfaces when applied/used in public eating places, dairy
processing equipment, and/or food processing equipment and utensils.
These tolerance exemptions are established on the Agency's own
initiative under the Federal Food, Drug, and Cosmetic Act (FFDCA), in
order to implement the tolerance actions EPA identified during its
review of these chemicals as part of the Agency's registration review
program under the Federal Insecticide, Fungicide, and Rodenticide Act
(FIFRA).
DATES: This regulation is effective January 31, 2024. Objections and
requests for hearings must be received on or before April 1, 2024, 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-2023-0225, 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. Please review the
visitor instructions and additional information about the docket
available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Anita Pease, Antimicrobials Division
(7510M), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave. NW, Washington, DC 20460-0001; main telephone
number: (202) 566-0736; 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 a
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 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-2023-0255 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 in the Office
of the Administrative Law Judges on or before April 1, 2024.
Notwithstanding the procedural requirements of 40 CFR 178.25(b), the
Office of the Administrative Law Judges has issued an order urging
parties to file and serve documents with the Tribunal by electronic
means only. See Revised Order Urging Electronic Filing and Service
(dated June 22, 2023), https://www.epa.gov/system/files/documents/2023-06/2023-06-22%20-%20revised%20order%20urging%20electronic%20filing%20and%20service.pdf.
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-2023-0225, 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.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
[[Page 6017]]
II. Background
A. Proposed Rule
In the Federal Register of May 5, 2023 (88 FR 29010) (FRL-10919-01-
OCSPP), EPA proposed to establish exemptions from the requirement of a
tolerance for residues of the antimicrobial pesticides ortho-benzyl-
para-chlorophenol, potassium 2-benzyl-4-chlorophenate, and sodium 2-
benzyl-4-chlorophenate in food resulting from application to food-
contact surfaces in public eating places, dairy-processing equipment,
and food-processing equipment and utensils. The Agency had identified
the need for the exemptions as part of the registration review process
under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA),
7 U.S.C. 136a(g), and published a proposed rulemaking under its
authority to initiate tolerance rulemakings under the FFDCA section
408(e), 21 U.S.C. 346a(e). That proposal noted that the new exemptions
would supersede the current exemption for ortho-benzyl-para-
chlorophenol under 40 CFR 180.940(c) (listed as phenol, 4-chloro-2-
(phenylmethyl)-, an alternative name for ortho-benzyl-para-
chlorophenol), which would be removed from the regulations as
unnecessary and redundant.
As noted in the proposal, the O-Benzyl-p-Chlorophenol (OBPCP)
Interim Registration Review Decision (OBPCP ID) identified the need for
these exemptions based on existing registered pesticide uses, and the
underlying risk assessment concluded that there were no risks of
concern associated with these uses. Consequently, EPA concluded that
the exemptions from the requirement of a tolerance for residues of
ortho-benzyl-para-chlorophenol, sodium 2-benzyl-4-chlorophenate, and
potassium 2-benzyl-4-chlorophenate, when used in antimicrobial
formulations applied to food contact surfaces in public eating places,
dairy processing equipment, and food processing equipment and utensils
when used at concentrations not to exceed 2,080 ppm in end-use
formulations, would be safe. Electronic copies of the OBPCP ID and
other documents are available in EPA docket number EPA-HQ-OPP-2011-
0423, which can be found at https://www.regulations.gov.
B. What is the Agency's authority for taking this action?
Under section 408(e) of the FFDCA, EPA can establish an exemption
from the requirement of a tolerance for residues of a pesticide
chemical after publishing a proposed rule and providing 60-day period
for public comment. 21 U.S.C. 346a(e). EPA published the proposed rule
on May 5, 2023, and provided 60 days for public comment (until July 5,
2023).
III. Final Rule
A. Comments
No substantive comments were submitted in response to the proposed
rule.
B. Determination of Safety
Section 408(c)(2)(A)(i) of FFDCA allows EPA to establish an
exemption from the requirement for a tolerance (the legal limit for a
pesticide chemical residue in or on a food) only if EPA determines that
the exemption is ``safe.'' Section 408(c)(2)(A)(ii) of FFDCA defines
``safe'' to mean that ``there is a reasonable certainty that no harm
will result from aggregate exposure to the pesticide chemical residue,
including all anticipated dietary exposures and all other exposures for
which there is reliable information.'' This includes exposure through
drinking water and in residential settings but does not include
occupational exposure. Pursuant to FFDCA section 408(c)(2)(B), in
establishing or maintaining in effect an exemption from the requirement
of a tolerance, EPA must take into account the factors set forth in
FFDCA section 408(b)(2)(C), which 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 . .
. .''
As noted in the proposed rule, EPA reviewed the available
scientific data and other relevant information as part of registration
review and in support of this action. Based on that review, EPA's
proposed rule concluded that the exemptions would be safe.
Since no comments were filed, EPA's assessment of the potential for
risks from exposure to these pesticide chemicals and conclusions about
the safety of these exemptions remains unchanged. Therefore, based on
the lack of any aggregate risks of concern, EPA concludes that these
exemptions from the requirement of a tolerance for residues of ortho-
benzyl-para-chlorophenol, sodium 2-benzyl-4-chlorophenate, and
potassium 2-benzyl-4-chlorophenate, including the limitation for the
end-use formulation concentration of each of these pesticides to not
exceed 2,080 ppm, are safe, i.e., there is a reasonable certainty that
no harm will result from aggregate exposures to ortho-benzyl-para-
chlorophenol, sodium 2-benzyl-4-chlorophenate, or potassium 2-benzyl-4-
chlorophenate, when used in accordance with the terms of the respective
exemptions. In addition, EPA has determined that there is a reasonable
certainty that no harm will result to infants and children from
aggregate exposure to the pesticide chemical residues, in accordance
with FFDCA section 408(b)(2)(C).
IV. Conclusion
Therefore, exemptions from the requirement of a tolerance are
established for residues of ortho-benzyl-para-chlorophenol, potassium
2-benzyl-4-chlorophenate, and sodium 2-benzyl-4-chlorophenate, when
used on or applied to food contact surfaces in public eating places,
dairy processing equipment, and food processing equipment and utensils,
with a limitation in concentration of 2,080 ppm in end-use
formulations. In addition, EPA is removing the existing exemption in 40
CFR 180.940(c) for residues of phenol, 4-chloro-2-(phenylmethyl)-, as
it is unnecessary and redundant upon the establishment of these new
exemptions.
V. Statutory and Executive Order Reviews
Additional information about these statutes and Executive orders
can be found at https://www.epa.gov/laws-regulations/laws-and-executive-orders#influence.
A. Executive Order 12866: Regulatory Planning and Review and Executive
Order 13563: Improving Regulations and Regulatory Review
This action is exempt from review by the Office of Management and
Budget (OMB) under Executive Orders 12866 (58 FR 51735, October 4,
1993) and 13563 (76 FR 3821, January 21, 2011) because it establishes
tolerance exemptions under FFDCA section 408.
B. Paperwork Reduction Act (PRA)
This action does not impose an information collection burden under
the PRA, 44 U.S.C. 3501 et seq., because it does not contain any
information collection activities.
C. Regulatory Flexibility Act (RFA)
I certify that this action will not have a significant economic
impact on a substantial number of small entities under the RFA, 5
U.S.C. 601 et seq. In making this determination, EPA concludes that the
impact of concern for this rule is any significant adverse economic
impact on small entities and
[[Page 6018]]
that the Agency is certifying that this rule will not have a
significant economic impact on a substantial number of small entities
because the rule has no net burden on small entities subject to the
rule. As discussed in the proposed rule, this takes into account the
EPA analysis for the establishment and modification of tolerances.
Furthermore, the Agency did not receive any comments on these
conclusions as presented in the proposed rule.
D. Unfunded Mandates Reform Act (UMRA)
This action does not contain any unfunded mandate as described in
UMRA, 2 U.S.C. 1531-1538, and does not significantly or uniquely affect
small governments. The action imposes no enforceable duty on any state,
local, or tribal governments or the private sector.
E. Executive Order 13132: Federalism
This action does not have federalism implications as specified in
Executive Order 13132, August 10, 1999 (64 FR 43255). It will not have
substantial direct effects on the states, on the relationship between
the National Government and the states, or on the distribution of power
and responsibilities among the various levels of government.
F. Executive Order 13175: Consultation and Coordination With Indian
Tribal Governments
This action does not have tribal implications as specified in
Executive Order 13175, November 9, 2000 (65 FR 67249), because it will
not have substantial direct effects on tribal governments, on the
relationship between the Federal Government and the Indian tribes, or
on the distribution of power and responsibilities between the Federal
Government and Indian tribes.
G. Executive Order 13045: Protection of Children From Environmental
Health Risks and Safety Risks
Executive Order 13045 (62 FR 19885, April 23, 1997) directs Federal
agencies to include an evaluation of health and safety effects of the
planned regulation on children in Federal health and safety standards
and explain why the regulation is preferable to potential effective and
reasonably feasible alternatives. This action is also not subject to
Executive Order 13045 because it is not a significant regulatory action
under section 3(f)(1) of Executive Order 12866 (See Unit V.A.) and
because EPA does not believe the environmental health or safety risks
addressed by this action present a disproportionate risk to children.
However, EPA's Policy on Children's Health applies to this action.
This rule finalizes tolerance actions under the FFDCA, which
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 . . .'' (FFDCA 408(b)(2)(C)). Consistent with FFDCA
section 408(b)(2)(D), and the factors specified therein, EPA has
reviewed the available scientific and other data and other relevant
information in support of these final tolerance actions. The Agency's
consideration is documented in the pesticide specific registration
review decision documents. See the discussion in Unit III. and access
the chemical specific registration review documents in each chemical
docket at https://www.regulations.gov.
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution or Use
This action is not a subject to Executive Order 13211 (66 FR 28355,
May 22, 2001) because it is not a significant regulatory action under
Executive Order 12866.
I. National Technology Transfer Advancement Act (NTTAA)
This action does not involve technical standards under NTTAA
section 12(d), 15 U.S.C. 272.
J. Executive Order 12898: Federal Actions To Address Environmental
Justice in Minority Populations and Low-Income Populations
Executive Order 12898 (59 FR 7629, February 16, 1994) directs
Federal agencies, to the greatest extent practicable and permitted by
law, to make environmental justice part of their mission by identifying
and addressing, as appropriate, disproportionately high and adverse
human health or environmental effects of their programs, policies, and
activities on minority populations (people of color and/or indigenous
peoples) and low-income populations. As discussed in more detail in the
pesticide specific risk assessments conducted as part of the
registration review for the pesticides identified in Unit II., EPA has
considered the safety risks for the pesticides subject to this
rulemaking and in the context of the tolerance actions set out in this
rulemaking. EPA believes that the human health and environmental
conditions that exist prior to this action do not result in
disproportionate and adverse effects on people of color, low-income
populations, and/or indigenous peoples. Furthermore, EPA believes that
this action is not likely to result in new disproportionate and adverse
effects on people of color, low-income populations, and/or indigenous
peoples.
K. Congressional Review Act (CRA)
This action is subject to the CRA, 5 U.S.C. 801 et seq., and EPA
will submit a rule report to each House of the Congress and to the
Comptroller General of the United States. 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 25, 2024.
Anita Pease,
Director, Antimicrobials Division, Office of Pesticide Programs.
Therefore, for the reasons stated in the preamble, EPA amends 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. Amend Sec. 180.940 by:
0
a. Adding in alphabetical order the entries ``Ortho-benzyl-para-
chlorophenol'', ``Potassium 2-benzyl-4-chlorophenate'', and ``Sodium 2-
benzyl-4-chlorophenate'' to table 1 to paragraph (a).
0
b. Removing the entry ``Phenol, 4-chloro-2-(phenylmethyl)-'' from the
table in paragraph (c).
The additions read as follows:
Sec. 180.940 Tolerance exemptions for active and inert ingredients
for use in antimicrobial formulations (Food-contact surface sanitizing
solutions).
* * * * *
(a) * * *
[[Page 6019]]
Table 1 to Paragraph (a)
------------------------------------------------------------------------
Pesticide chemical CAS reg. No. Limits
------------------------------------------------------------------------
* * * * * * *
Ortho-benzyl-para-chlorophenol. 120-32-1 When ready for use, the
end-use concentration
is not to exceed 2080
ppm.
* * * * * * *
Potassium 2-benzyl-4- 35471-49-9 When ready for use, the
chlorophenate. end-use concentration
is not to exceed 2080
ppm.
* * * * * * *
Sodium 2-benzyl-4-chlorophenate 3184-65-4 When ready for use, the
end-use concentration
is not to exceed 2080
ppm.
* * * * * * *
------------------------------------------------------------------------
* * * * *
[FR Doc. 2024-01869 Filed 1-30-24; 8:45 am]
BILLING CODE 6560-50-P