Poly(oxy-1,2-ethanediyl)-α-hydro-ω-hydroxy-, Polymer With Poly(isocyanatoalkyl) Benzene, Alkylol-Blocked; Tolerance Exemption, 6039-6042 [2022-02100]
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Federal Register / Vol. 87, No. 23 / Thursday, February 3, 2022 / Rules and Regulations
effectuate this rule, under 38 CFR
3.317(a)(1)(i), VA replaced the phrase
‘‘not later than December 31, 2021’’ with
‘‘not later than December 31, 2026.’’
Under the provisions of 5 U.S.C.
553(b)(B) and (d)(3) the Secretary of
Veterans Affairs found that there was
good cause to publish this rule without
prior opportunity for public comment.
Had VA not extended the sunset date for
the regulation, its authority to provide
benefits in new claims for qualifying
chronic disability in Gulf War veterans
would have lapsed on December 31,
2021. A lapse of such authority would
have been contrary to the public interest
because it would have had a significant
adverse impact on veterans disabled due
to such disabilities. To avoid such
impact, VA issued this rule as an
interim final rule. However, VA invited
interested persons to submit written
comments on or before October 14,
2021, and received seven comments in
response to the interim final rule. These
comments are discussed below.
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General Comments
Three commenters referenced their
poor health concerns or the poor health
concerns of a family member. While VA
sympathizes with anyone suffering from
a debilitating disability and/or disease,
the scope of this rule only addresses the
deadline for the manifestation of
presumptive conditions. VA makes no
changes based on these comments.
One commenter suggested the
regulation should contain VA’s
definition of Southwest Asia. This rule
merely extends the presumption period
in 38 CFR 3.317, and that section
already contains VA’s definition of the
Southwest Asia theater of operations (in
38 CFR 3.317(e)(2)). VA makes no
changes based on this comment.
One commenter suggested that since
no end date for the Persian Gulf War has
been established by Congress, any
deadline is premature. However, this
rule does not impose a deadline; it
extends the presumptive period during
which disabilities associated with
undiagnosed illnesses and medically
unexplained chronic multi-symptom
illnesses must become manifest in order
for a veteran to be eligible for
compensation based on the
presumption. VA makes no changes
based on this comment.
VA received two non-substantive
comments. VA makes no changes based
on these comments.
As VA makes no changes based on the
comments received, this document
adopts as a final rule the interim final
rule published in the Federal Register
on September 14, 2021.
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Executive Orders 12866 and 13563
Executive Orders 12866 and 13563
direct agencies to assess the costs and
benefits of available regulatory
alternatives and, when regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, and other advantages;
distributive impacts; and equity).
Executive Order 13563 (Improving
Regulation and Regulatory Review)
emphasizes the importance of
quantifying both costs and benefits,
reducing costs, harmonizing rules, and
promoting flexibility. The Office of
Information and Regulatory Affairs has
determined that this rule is not a
significant regulatory action under
Executive Order 12866. The Regulatory
Impact Analysis associated with this
rulemaking can be found as a
supporting document at
www.regulations.gov.
Regulatory Flexibility Act
The Secretary hereby certifies that
this final rule will not have a significant
economic impact on a substantial
number of small entities as they are
defined in the Regulatory Flexibility Act
(5 U.S.C. 601–612). There are no small
entities involved with the process and/
or benefits associated with the
rulemaking. Therefore, pursuant to 5
U.S.C. 605(b), the initial and final
regulatory flexibility analysis
requirements of 5 U.S.C. 603 and 604 do
not apply.
Unfunded Mandates
The Unfunded Mandates Reform Act
of 1995 requires, at 2 U.S.C. 1532, that
agencies prepare an assessment of
anticipated costs and benefits before
issuing any rule that may result in the
expenditure by state, local, and tribal
governments, in the aggregate, or by the
private sector, of $100 million or more
(adjusted annually for inflation) in any
one year. This final rule will have no
such effect on state, local, and tribal
governments, or on the private sector.
Paperwork Reduction Act
This final rule contains no provisions
constituting a collection of information
under the Paperwork Reduction Act of
1995 (44 U.S.C. 3501–3521).
Catalog of Federal Domestic Assistance
The Catalog of Federal Domestic
Assitance numbers and titles for this
rule are: 64.104, Pension for NonService-Connected Disability for
Veterans; 64.109, Veterans
Compensation for Service-Connected
Disability.
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Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), the Office of
Information and Regulatory Affairs
designated this rule as not a major rule,
as defined by 5 U.S.C. 804(2).
List of Subjects in 38 CFR Part 3
Administrative practice and
procedure, Claims, Disability benefits,
Pensions, Veterans.
Signing Authority
Denis McDonough, Secretary of
Veterans Affairs, approved this
document on January 19, 2022, and
authorized the undersigned to sign and
submit the document to the Office of the
Federal Register for publication
electronically as an official document of
the Department of Veterans Affairs.
Luvenia Potts,
Regulation Development Coordinator, Office
of Regulation Policy & Management, Office
of General Counsel, Department of Veterans
Affairs.
For the reasons set forth in the
preamble, the Department of Veterans
Affairs adopts the interim rule
published September 14, 2021, at 86 FR
51000, as final without change.
■
[FR Doc. 2022–02176 Filed 2–2–22; 8:45 am]
BILLING CODE 8320–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2021–0680; FRL–9399–01–
OCSPP]
Poly(oxy-1,2-ethanediyl)-α-hydro-whydroxy-, Polymer With
Poly(isocyanatoalkyl) Benzene,
Alkylol-Blocked; Tolerance Exemption
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes an
exemption from the requirement of a
tolerance for residues of Poly(oxy-1,2ethanediyl)-a-hydro-w-hydroxy-,
polymer with poly(isocyanatoalkyl)
benzene, alkylol-blocked when used as
an inert ingredient in a pesticide
chemical formulation. BYK USA Inc.
submitted a petition to EPA under the
Federal Food, Drug, and Cosmetic Act
(FFDCA), requesting an exemption from
the requirement of a tolerance. This
regulation eliminates the need to
establish a maximum permissible level
for residues of Poly(oxy-1,2-ethanediyl)a-hydro-w-hydroxy-, polymer with
SUMMARY:
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Federal Register / Vol. 87, No. 23 / Thursday, February 3, 2022 / Rules and Regulations
poly(isocyanatoalkyl) benzene, alkylolblocked on food or feed commodities.
DATES: This regulation is effective
February 3, 2022. Objections and
requests for hearings must be received
on or before April 4, 2022, and must be
filed in accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
B. How can I get electronic access to
other related information?
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2021–0680, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805.
Due to the public health concerns
related to COVID–19, the EPA Docket
Center (EPA/DC) and Reading Room is
closed to visitors with limited
exceptions. The staff continues to
provide remote customer service via
email, phone, and webform. For the
latest status information on EPA/DC
services and docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Marietta Echeverria, Registration
Division (7505P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; main
telephone number: (703) 305–7090;
email address: RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
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–2021–0680 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 April
4, 2022. Addresses for mail and hand
delivery of objections and hearing
requests are provided in 40 CFR
178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
disclosed publicly by EPA without prior
notice. Submit the non-CBI copy of your
objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2021–0680, 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.
ADDRESSES:
I. General Information
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A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
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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. Can I file an objection or hearing
request?
II. Background and Statutory Findings
In the Federal Register of October 21,
2021 (86 FR 58239) (FRL–8792–04–
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OCSPP), EPA issued a document
pursuant to FFDCA section 408, 21
U.S.C. 346a, announcing the receipt of
a pesticide petition (PP IN–11586) filed
by BYK USA Inc., 524 South Cherry St.,
Wallingford, CT 06492. The petition
requested that 40 CFR 180.960 be
amended by establishing an exemption
from the requirement of a tolerance for
residues of Poly(oxy-1,2-ethanediyl)-ahydro-w-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked (No CAS Reg. No Associated).
That document included a summary of
the petition prepared by the petitioner
and solicited comments on the
petitioner’s request. The Agency did not
receive any comments.
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
use in residential settings but does not
include occupational exposure. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing an
exemption from the requirement of 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 . . .’’ and specifies
factors EPA is to consider in
establishing an exemption.
III. Risk Assessment and Statutory
Findings
EPA establishes exemptions from the
requirement of a tolerance only in those
cases where it can be shown that the
risks from aggregate exposure to
pesticide chemical residues under
reasonably foreseeable circumstances
will pose no appreciable risks to human
health. In order to determine the risks
from aggregate exposure to pesticide
inert ingredients, the Agency considers
the toxicity of the inert in conjunction
with possible exposure to residues of
the inert ingredient through food,
drinking water, and through other
exposures that occur as a result of
pesticide use in residential settings. If
EPA is able to determine that a finite
tolerance is not necessary to ensure that
there is a reasonable certainty that no
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Federal Register / Vol. 87, No. 23 / Thursday, February 3, 2022 / Rules and Regulations
harm will result from aggregate
exposure to the inert ingredient, an
exemption from the requirement of a
tolerance may be established.
Consistent with FFDCA section
408(b)(2)(D), EPA has reviewed the
available scientific data and other
relevant information in support of this
action and considered its validity,
completeness and reliability and the
relationship of this information to
human risk. EPA has also considered
available information concerning the
variability of the sensitivities of major
identifiable subgroups of consumers,
including infants and children. In the
case of certain chemical substances that
are defined as polymers, the Agency has
established a set of criteria to identify
categories of polymers expected to
present minimal or no risk. The
definition of a polymer is given in 40
CFR 723.250(b) and the exclusion
criteria for identifying these low-risk
polymers are described in 40 CFR
723.250(d). Poly(oxy-1,2-ethanediyl)-ahydro-w-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked conforms to the definition of a
polymer given in 40 CFR 723.250(b) and
meets the following criteria that are
used to identify low-risk polymers.
1. The polymer is not a cationic
polymer nor is it reasonably anticipated
to become a cationic polymer in a
natural aquatic environment.
2. The polymer does contain as an
integral part of its composition at least
two of the atomic elements carbon,
hydrogen, nitrogen, oxygen, silicon, and
sulfur.
3. The polymer does not contain as an
integral part of its composition, except
as impurities, any element other than
those listed in 40 CFR 723.250(d)(2)(ii).
4. The polymer is neither designed
nor can it be reasonably anticipated to
substantially degrade, decompose, or
depolymerize.
5. The polymer is manufactured or
imported from monomers and/or
reactants that are already included on
the TSCA Chemical Substance
Inventory or manufactured under an
applicable TSCA section 5 exemption.
6. The polymer is not a water
absorbing polymer with a number
average molecular weight (MW) greater
than or equal to 10,000 daltons.
7. The polymer does not contain
certain perfluoroalkyl moieties
consisting of a CF3- or longer chain
length as listed in 40 CFR 723.250(d)(6).
Additionally, the polymer also meets
as required the following exemption
criteria specified in 40 CFR 723.250(e).
8. The polymer’s number average MW
of 18,721 Daltons is greater than or
equal to 10,000 daltons. However, the
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polymer contains less than 2%
oligomeric material below MW 500 (0%)
and less than 5% oligomeric material
below MW 1,000 (1.1%).
Thus, Poly(oxy-1,2-ethanediyl)-ahydro-w-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked meets the criteria for a polymer
to be considered low risk under 40 CFR
723.250. Based on its conformance to
the criteria in this unit, no mammalian
toxicity is anticipated from dietary,
inhalation, or dermal exposure to
Poly(oxy-1,2-ethanediyl)-a-hydro-mhydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked.
IV. Aggregate Exposures
For the purposes of assessing
potential exposure under this
exemption, EPA considered that
Poly(oxy-1,2-ethanediyl)-a-hydro-whydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked could be present in all raw and
processed agricultural commodities and
drinking water, and that nonoccupational non-dietary exposure was
possible. The number average MW of
Poly(oxy-1,2-ethanediyl)-a-hydro-whydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked is 18,721 daltons. Generally, a
polymer of this size would be poorly
absorbed through the intact
gastrointestinal tract or through intact
human skin. Since Poly(oxy-1,2ethanediyl)-a-hydro-w-hydroxy-,
polymer with poly(isocyanatoalkyl)
benzene, alkylol-blocked conforms to
the criteria that identify a low-risk
polymer, there are no concerns for risks
associated with any potential exposure
scenarios that are reasonably
foreseeable. The Agency has determined
that a tolerance is not necessary to
protect the public health.
V. Cumulative Effects From Substances
With a Common Mechanism of Toxicity
Section 408(b)(2)(D)(v) of FFDCA
requires that, when considering whether
to establish, modify, or revoke a
tolerance, the Agency consider
‘‘available information’’ concerning the
cumulative effects of a particular
pesticide’s residues and ‘‘other
substances that have a common
mechanism of toxicity.’’ EPA has not
found Poly(oxy-1,2-ethanediyl)-ahydro-w-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked to share a common mechanism
of toxicity with any other substances,
and Poly(oxy-1,2-ethanediyl)-a-hydrow-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked does not appear to produce a
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6041
toxic metabolite produced by other
substances. For the purposes of this
tolerance action, therefore, EPA has
assumed Poly(oxy-1,2-ethanediyl)-ahydro-w-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked does not have a common
mechanism of toxicity with other
substances. For information regarding
EPA’s efforts to determine which
chemicals have a common mechanism
of toxicity and to evaluate the
cumulative effects of such chemicals,
see EPA’s website at https://
www.epa.gov/pesticides/cumulative.
VI. Determination of Safety
Based on the conformance to the
criteria used to identify a low-risk
polymer, EPA concludes that there is a
reasonable certainty of no harm to the
U.S. population, including infants and
children, from aggregate exposure to
residues of Poly(oxy-1,2-ethanediyl)-ahydro-w-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked.
VII. Other Considerations
Analytical Enforcement Methodology
An analytical method is not required
for enforcement purposes since the
Agency is establishing an exemption
from the requirement of a tolerance
without any numerical limitation.
VIII. Conclusion
Accordingly, EPA finds that
exempting residues of Poly(oxy-1,2ethanediyl)-a-hydro-w-hydroxy-,
polymer with poly(isocyanatoalkyl)
benzene, alkylol-blocked from the
requirement of a tolerance will be safe.
IX. Statutory and Executive Order
Reviews
This action establishes a tolerance
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997). This action does not
contain any information collections
subject to OMB approval under the
Paperwork Reduction Act (PRA) (44
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U.S.C. 3501 et seq.), nor does it require
any special considerations under
Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerance in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or Tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
has determined that this action will not
have a substantial direct effect on States
or Tribal Governments, on the
relationship between the National
Government and the States or Tribal
Governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
Tribes. Thus, the Agency has
determined that Executive Order 13132,
entitled ‘‘Federalism’’ (64 FR 43255,
August 10, 1999) and Executive Order
13175, entitled ‘‘Consultation and
Coordination with Indian Tribal
Governments’’ (65 FR 67249, November
9, 2000) do not apply to this action. In
addition, this action does not impose
any enforceable duty or contain any
unfunded mandate as described under
Title II of the Unfunded Mandates
Reform Act (UMRA) (2 U.S.C. 1501 et
seq.).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
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 20, 2022.
Marietta Echeverria,
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.
X. 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).
2. In § 180.960, amend table 1 by
adding, in alphabetical order, the
polymer ‘‘Poly(oxy-1,2-ethanediyl)-ahydro-w-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylolblocked, number average molecular
weight (Mn), 18,721’’ to read as follows:
■
§ 180.960 Polymers; exemptions from the
requirement of a tolerance.
*
*
*
*
Polymer
CAS No.
*
*
*
*
*
Poly(oxy-1,2-ethanediyl)-a-hydro-w-hydroxy-, polymer with poly(isocyanatoalkyl) benzene, alkylol-blocked,
number average molecular weight (Mn), 18,721.
*
*
*
[FR Doc. 2022–02100 Filed 2–2–22; 8:45 am]
BILLING CODE 6560–50–P
GENERAL SERVICES
ADMINISTRATION
41 CFR Parts 102–35 and 102–37
[FMR Case 2018–102–6; Docket No. GSA–
FMR–2019–0007, Sequence No. 2]
RIN 3090–AJ98
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Federal Management Regulation
(FMR); Personal Property; Multiple
Repeal or Replace Regulatory Actions;
Multiple FMR Parts
GSA is issuing a final rule to
modify provisions in the Federal
SUMMARY:
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16:34 Feb 02, 2022
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*
Management Regulation (FMR) to
improve readability and ease of use by
reorganizing certain FMR parts to reflect
the asset management life-cycle and by
updating the definition of a ‘museum’.
DATES: Effective: March 7, 2022.
FOR FURTHER INFORMATION CONTACT: Mr.
William Garrett, Program Director,
Office of Government-wide Policy, at
202–368–8163, for clarification of
content. For information pertaining to
status or publication schedules, contact
the Regulatory Secretariat at 202–501–
4755. Please cite FMR Case 2018–102–
6.
SUPPLEMENTARY INFORMATION:
This final rule amends the FMR to
improve readability and ease of use.
Specifically, it reorganizes certain FMR
parts to reflect the asset management
life-cycle and updates the definition of
a ‘museum’.
PO 00000
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*
*
(No CAS Reg. No. Associated).
*
I. Background
Office of Government-wide
Policy (OGP), General Services
Administration (GSA).
ACTION: Final rule.
AGENCY:
*
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*
*
GSA sought public comments on
improving FMR regulations through a
Federal Register document (MA–2017–
03) published on May 30, 2017, at 82 FR
24651. Concurrently, GSA sought
comments and recommendations from
agencies, GSA subject matter experts,
and other stakeholders and customers.
The two substantive/germane
comments and recommendations
elicited from the Federal Register
document were reviewed by GSA and
are addressed in this rule. Two other
recommendations addressing (1) agency
asset management systems and (2) use
of voluntary consensus standards were
not included in this rule as GSA does
not have the legal authority to
promulgate regulations addressing
property in use by an agency before it
is reported to GSA as excess personal
property.
Provisions in this final rule make the
FMR policies addressing personal
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Agencies
[Federal Register Volume 87, Number 23 (Thursday, February 3, 2022)]
[Rules and Regulations]
[Pages 6039-6042]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-02100]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2021-0680; FRL-9399-01-OCSPP]
Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, Polymer
With Poly(isocyanatoalkyl) Benzene, Alkylol-Blocked; Tolerance
Exemption
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes an exemption from the requirement
of a tolerance for residues of Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-
[omega]-hydroxy-, polymer with poly(isocyanatoalkyl) benzene, alkylol-
blocked when used as an inert ingredient in a pesticide chemical
formulation. BYK USA Inc. submitted a petition to EPA under the Federal
Food, Drug, and Cosmetic Act (FFDCA), requesting an exemption from the
requirement of a tolerance. This regulation eliminates the need to
establish a maximum permissible level for residues of Poly(oxy-1,2-
ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, polymer with
[[Page 6040]]
poly(isocyanatoalkyl) benzene, alkylol-blocked on food or feed
commodities.
DATES: This regulation is effective February 3, 2022. Objections and
requests for hearings must be received on or before April 4, 2022, and
must be filed in accordance with the instructions provided in 40 CFR
part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2021-0680, is available at
https://www.regulations.gov or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket) in the Environmental Protection
Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg.,
Rm. 3334, 1301 Constitution Ave. NW, Washington, DC 20460-0001. The
Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805.
Due to the public health concerns related to COVID-19, the EPA
Docket Center (EPA/DC) and Reading Room is closed to visitors with
limited exceptions. The staff continues to provide remote customer
service via email, phone, and webform. For the latest status
information on EPA/DC services and docket access, visit https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Marietta Echeverria, Registration
Division (7505P), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-
0001; main telephone number: (703) 305-7090; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other 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. 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-2021-0680 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
April 4, 2022. Addresses for mail and hand delivery of objections and
hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be disclosed publicly by EPA without
prior notice. Submit the non-CBI copy of your objection or hearing
request, identified by docket ID number EPA-HQ-OPP-2021-0680, 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. Background and Statutory Findings
In the Federal Register of October 21, 2021 (86 FR 58239) (FRL-
8792-04-OCSPP), EPA issued a document pursuant to FFDCA section 408, 21
U.S.C. 346a, announcing the receipt of a pesticide petition (PP IN-
11586) filed by BYK USA Inc., 524 South Cherry St., Wallingford, CT
06492. The petition requested that 40 CFR 180.960 be amended by
establishing an exemption from the requirement of a tolerance for
residues of Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-[omega]-hydroxy-,
polymer with poly(isocyanatoalkyl) benzene, alkylol-blocked (No CAS
Reg. No Associated). That document included a summary of the petition
prepared by the petitioner and solicited comments on the petitioner's
request. The Agency did not receive any comments.
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 use in residential settings but does not include
occupational exposure. Section 408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure of infants and children to the
pesticide chemical residue in establishing an exemption from the
requirement of 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 . . .'' and
specifies factors EPA is to consider in establishing an exemption.
III. Risk Assessment and Statutory Findings
EPA establishes exemptions from the requirement of a tolerance only
in those cases where it can be shown that the risks from aggregate
exposure to pesticide chemical residues under reasonably foreseeable
circumstances will pose no appreciable risks to human health. In order
to determine the risks from aggregate exposure to pesticide inert
ingredients, the Agency considers the toxicity of the inert in
conjunction with possible exposure to residues of the inert ingredient
through food, drinking water, and through other exposures that occur as
a result of pesticide use in residential settings. If EPA is able to
determine that a finite tolerance is not necessary to ensure that there
is a reasonable certainty that no
[[Page 6041]]
harm will result from aggregate exposure to the inert ingredient, an
exemption from the requirement of a tolerance may be established.
Consistent with FFDCA section 408(b)(2)(D), EPA has reviewed the
available scientific data and other relevant information in support of
this action and considered its validity, completeness and reliability
and the relationship of this information to human risk. EPA has also
considered available information concerning the variability of the
sensitivities of major identifiable subgroups of consumers, including
infants and children. In the case of certain chemical substances that
are defined as polymers, the Agency has established a set of criteria
to identify categories of polymers expected to present minimal or no
risk. The definition of a polymer is given in 40 CFR 723.250(b) and the
exclusion criteria for identifying these low-risk polymers are
described in 40 CFR 723.250(d). Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-
[omega]-hydroxy-, polymer with poly(isocyanatoalkyl) benzene, alkylol-
blocked conforms to the definition of a polymer given in 40 CFR
723.250(b) and meets the following criteria that are used to identify
low-risk polymers.
1. The polymer is not a cationic polymer nor is it reasonably
anticipated to become a cationic polymer in a natural aquatic
environment.
2. The polymer does contain as an integral part of its composition
at least two of the atomic elements carbon, hydrogen, nitrogen, oxygen,
silicon, and sulfur.
3. The polymer does not contain as an integral part of its
composition, except as impurities, any element other than those listed
in 40 CFR 723.250(d)(2)(ii).
4. The polymer is neither designed nor can it be reasonably
anticipated to substantially degrade, decompose, or depolymerize.
5. The polymer is manufactured or imported from monomers and/or
reactants that are already included on the TSCA Chemical Substance
Inventory or manufactured under an applicable TSCA section 5 exemption.
6. The polymer is not a water absorbing polymer with a number
average molecular weight (MW) greater than or equal to 10,000 daltons.
7. The polymer does not contain certain perfluoroalkyl moieties
consisting of a CF3- or longer chain length as listed in 40 CFR
723.250(d)(6).
Additionally, the polymer also meets as required the following
exemption criteria specified in 40 CFR 723.250(e).
8. The polymer's number average MW of 18,721 Daltons is greater
than or equal to 10,000 daltons. However, the polymer contains less
than 2% oligomeric material below MW 500 (0%) and less than 5%
oligomeric material below MW 1,000 (1.1%).
Thus, Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-[omega]-hydroxy-,
polymer with poly(isocyanatoalkyl) benzene, alkylol-blocked meets the
criteria for a polymer to be considered low risk under 40 CFR 723.250.
Based on its conformance to the criteria in this unit, no mammalian
toxicity is anticipated from dietary, inhalation, or dermal exposure to
Poly(oxy-1,2-ethanediyl)-a-hydro-m-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylol-blocked.
IV. Aggregate Exposures
For the purposes of assessing potential exposure under this
exemption, EPA considered that Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-
[omega]-hydroxy-, polymer with poly(isocyanatoalkyl) benzene, alkylol-
blocked could be present in all raw and processed agricultural
commodities and drinking water, and that non-occupational non-dietary
exposure was possible. The number average MW of Poly(oxy-1,2-
ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylol-blocked is 18,721 daltons.
Generally, a polymer of this size would be poorly absorbed through the
intact gastrointestinal tract or through intact human skin. Since
Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylol-blocked conforms to the criteria
that identify a low-risk polymer, there are no concerns for risks
associated with any potential exposure scenarios that are reasonably
foreseeable. The Agency has determined that a tolerance is not
necessary to protect the public health.
V. Cumulative Effects From Substances With a Common Mechanism of
Toxicity
Section 408(b)(2)(D)(v) of FFDCA requires that, when considering
whether to establish, modify, or revoke a tolerance, the Agency
consider ``available information'' concerning the cumulative effects of
a particular pesticide's residues and ``other substances that have a
common mechanism of toxicity.'' EPA has not found Poly(oxy-1,2-
ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylol-blocked to share a common
mechanism of toxicity with any other substances, and Poly(oxy-1,2-
ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylol-blocked does not appear to
produce a toxic metabolite produced by other substances. For the
purposes of this tolerance action, therefore, EPA has assumed Poly(oxy-
1,2-ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylol-blocked does not have a common
mechanism of toxicity with other substances. For information regarding
EPA's efforts to determine which chemicals have a common mechanism of
toxicity and to evaluate the cumulative effects of such chemicals, see
EPA's website at https://www.epa.gov/pesticides/cumulative.
VI. Determination of Safety
Based on the conformance to the criteria used to identify a low-
risk polymer, EPA concludes that there is a reasonable certainty of no
harm to the U.S. population, including infants and children, from
aggregate exposure to residues of Poly(oxy-1,2-ethanediyl)-[alpha]-
hydro-[omega]-hydroxy-, polymer with poly(isocyanatoalkyl) benzene,
alkylol-blocked.
VII. Other Considerations
Analytical Enforcement Methodology
An analytical method is not required for enforcement purposes since
the Agency is establishing an exemption from the requirement of a
tolerance without any numerical limitation.
VIII. Conclusion
Accordingly, EPA finds that exempting residues of Poly(oxy-1,2-
ethanediyl)-[alpha]-hydro-[omega]-hydroxy-, polymer with
poly(isocyanatoalkyl) benzene, alkylol-blocked from the requirement of
a tolerance will be safe.
IX. Statutory and Executive Order Reviews
This action establishes a tolerance under FFDCA section 408(d) in
response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001) or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997). This action does not contain any
information collections subject to OMB approval under the Paperwork
Reduction Act (PRA) (44
[[Page 6042]]
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 tolerance in this
final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or Tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
Tribal Governments, on the relationship between the National Government
and the States or Tribal Governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian Tribes. Thus, the Agency has
determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999) and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November 9, 2000) do not apply to this action. In addition, this
action does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
(UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
X. 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 20, 2022.
Marietta Echeverria,
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. 180.960, amend table 1 by adding, in alphabetical order,
the polymer ``Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-[omega]-hydroxy-,
polymer with poly(isocyanatoalkyl) benzene, alkylol-blocked, number
average molecular weight (Mn), 18,721'' to read as follows:
Sec. 180.960 Polymers; exemptions from the requirement of a
tolerance.
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Polymer CAS No.
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* * * * * * *
Poly(oxy-1,2-ethanediyl)-[alpha]-hydro-[omega]-hydroxy- (No CAS Reg. No. Associated).
, polymer with poly(isocyanatoalkyl) benzene, alkylol-
blocked, number average molecular weight (Mn), 18,721.
* * * * * * *
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[FR Doc. 2022-02100 Filed 2-2-22; 8:45 am]
BILLING CODE 6560-50-P