Sulfur Dioxide; Pesticide Tolerances, 68909-68911 [2022-25014]
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Federal Register / Vol. 87, No. 221 / Thursday, November 17, 2022 / Rules and Regulations
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2021–0203; FRL–10212–01–
OCSPP]
Sulfur Dioxide; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
B. How can I get electronic access to
other related information?
This regulation establishes a
tolerance for residues of sulfur dioxide
in or on blueberry. Interregional
Research Project Number 4 (IR–4)
requested this tolerance under the
Federal Food, Drug, and Cosmetic Act
(FFDCA).
DATES: This regulation is effective
November 17, 2022. Objections and
requests for hearings must be received
on or before January 17, 2023, and must
be filed in accordance with the
instructions provided in 40 CFR part
178 (see also Unit I.C. of the
SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2021–0203, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room and the OPP
Docket is (202) 566–1744. For the latest
status information on EPA/DC services,
docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Daniel Rosenblatt, Registration Division
(7505T), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; main telephone number:
(202) 566–1030; email address:
RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
lotter on DSK11XQN23PROD with RULES1
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
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Jkt 259001
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).
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Office of the Federal Register’s eCFR site at https://www.ecfr.gov/
current/title-40.
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2021–0203 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
January 17, 2023. Addresses for mail
and hand delivery of objections and
hearing requests are provided in 40 CFR
178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
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–
2021–0203, 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
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68909
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
II. Summary of Petitioned-For
Tolerance
In the Federal Register of June 28,
2021 (86 FR 33922) (FRL–10025–08),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide petition (PP 0E8894) by IR–4,
North Carolina State University, 1730
Varsity Drive, Venture IV, Suite 210,
Raleigh, NC 27606. The petition
requested to amend 40 CFR part 180 by
establishing tolerances for residues of
sulfur dioxide, including its metabolite
and degradates, in or on blueberry at 9
parts per million (ppm). That document
referenced a summary of the petition
prepared by IR–4, the petitioner, which
is available in the docket, https://
www.regulations.gov. Two comments
were received on the notice of filing
from the United States Department of
Agriculture and the North American
Blueberry Council. Both were in support
of the action.
III. Aggregate Risk Assessment and
Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA
allows EPA to establish a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(b)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings but does not include
occupational exposure. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing a
tolerance and to ‘‘ensure that there is a
reasonable certainty that no harm will
result to infants and children from
aggregate exposure to the pesticide
chemical residue.. . .’’
Consistent with FFDCA section
408(b)(2)(D), and the factors specified in
FFDCA section 408(b)(2)(D), EPA has
reviewed the available scientific data
and other relevant information in
support of this action. EPA has
sufficient data to assess the hazards of
and to make a determination on
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aggregate exposure for sulfur dioxide
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with these inorganic sulfites
follow.
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A. Toxicological Profile
There is a large volume of published
data detailing the toxicity of sulfur
dioxide and sodium metabisulfite, and
consequently the toxicity of these
pesticides has been well established.
Sodium metabisulfite pads generate
sulfur dioxide gas which then reacts
with foods to quickly form sulfite. In
addition to the use of sodium
metabisulfite pads, direct application of
sulfur dioxide gas is proposed for
blueberry treatments. For both
treatments, sulfite is the residue of
concern in food and is determined by
the analytical enforcement method.
EPA’s Office of Air Quality Planning
and Standards (OAQPS) has worked
extensively on sulfur dioxide, including
setting national ambient air quality
standards (NAAQS) for sulfur dioxide, a
gaseous air pollutant. The U.S. Food
and Drug Administration (FDA) has also
performed an extensive review of
sulfiting agents (including sulfur
dioxide, sodium metabisulfite, and
sodium bisulfite) that have been added
to any food or to any ingredient in any
food. For the dietary assessment, EPA is
relying on the established FDA
regulatory value for sulfite.
Sulfiting agents are used to add
sulfites to foods and include sulfur
dioxide, sodium metabisulfite, sodium
bisulfite, sodium sulfite, potassium
metabisulfite, and potassium bisulfite.
Humans may experience sensitivity
reactions following exposure to sulfites
including, but not limited to, diarrhea,
headache, difficulty breathing, vomiting
and nausea, and abdominal pain and
cramps. Asthmatics account for many,
but not necessarily all, of the
individuals who have a sensitivity to
sulfites. Given the known effects to
certain individuals within the
population, the FDA requires that any
food that contains a sulfiting agent at ≥
10 ppm or mg/kg be declared as such on
the food label.
Additional information on the
toxicological profile can be found at
https://www.regulations.gov in the
document titled ‘‘Inorganic Sulfites.
Human Health Risk Assessment in
Support of a Section 3 Registration for
Postharvest Fumigation of Blueberry’’
(hereinafter ‘‘Sulfur Dioxide Human
Health Risk Assessment’’) in docket ID
number EPA–HQ–OPP–2021–0203.
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B. Toxicological Points of Departure/
Levels of Concern
No appropriate toxicological
endpoints were selected for sulfur
dioxide. The Agency is relying on the
FDA-established regulatory level of up
to 10 ppm sulfite residues in foods.
C. Exposure Assessment
1. Dietary exposure from food and
feed uses. In evaluating dietary
exposure to sulfur dioxide, EPA
compared exposure from residues on
blueberries to the FDA-established
regulatory level. EPA assessed dietary
exposures from these inorganic sulfites
in food as follows:
Sulfite is the residue of concern for
consumption of treated blueberries. A
quantitative dietary assessment was not
conducted for sulfite since no
appropriate toxicological endpoints
were selected. The Agency is relying on
the FDA-established regulatory level of
up to 10 ppm sulfite residues in foods.
Residues of sulfites in blueberry from
sulfur dioxide and sodium metabisulfite
applications are expected to be below
the 10 ppm level when applied as tested
in the blueberry residue trials.
EPA did not use anticipated residue
or PCT information in the dietary
assessment for sulfur dioxide.
2. Dietary exposure from drinking
water. No residues are expected in
drinking water based on the current use
pattern, which includes post-harvest
fumigant treatment in a chamber and
slow release or dual release pads that
are placed in the clamshells used to
distribute blueberries.
3. From non-dietary exposure. The
term ‘‘residential exposure’’ is used in
this document to refer to nonoccupational, non-dietary exposure
(e.g., for lawn and garden pest control,
indoor pest control, termiticides, and
flea and tick control on pets).
There are no uses of sulfur dioxide or
sodium metabisulfite resulting in direct
residential exposures; therefore,
residential exposure is not expected.
4. 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.’’
Unlike other pesticides for which EPA
has followed a cumulative risk approach
based on a common mechanism of
toxicity, EPA has not made a common
mechanism of toxicity finding as to the
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inorganic sulfites and any other
substances and the inorganic sulfites do
not appear to produce a toxic metabolite
produced by other substances. For the
purposes of this tolerance action,
therefore, EPA has not assumed that the
inorganic sulfites have a common
mechanism of toxicity with other
substances.
D. Safety Factor for Infants and
Children
1. In general. Section 408(b)(2)(C) of
FFDCA provides that EPA shall apply
an additional tenfold (10X) margin of
safety for infants and children in the
case of threshold effects to account for
prenatal and postnatal toxicity and the
completeness of the database on toxicity
and exposure unless EPA determines
based on reliable data that a different
margin of safety will be safe for infants
and children. This additional margin of
safety is commonly referred to as the
Food Quality Protection Act Safety
Factor (FQPA)(SF). In applying this
provision, EPA either retains the default
value of 10X, or uses a different
additional safety factor when reliable
data available to EPA support the choice
of a different factor.
Consistent with the factors specified
in FFDCA section 408(b)(2)(D), EPA has
also reviewed the available scientific
data and other relevant information in
support of regulations establishing the
10 ppm maximum permissible level for
residues of sulfur dioxide to support a
time-limited tolerance of sulfur dioxide
residues in or on fig (September 14,
2011; 76 FR 56644) (FRL–8887–2). EPA
also considered available information
concerning the variability of the
sensitivities of major identifiable
subgroups of consumers, including
sulfite sensitive individuals, infants,
and children. EPA has concluded that
there is sufficient toxicological
information for sulfur dioxide to
address risks to infants and children. In
addition, the available information
indicated that there is no evidence of
increased quantitative or qualitative
susceptibility of the offspring after in
utero or postnatal exposure. Based on
the lack of observed susceptibility, and
since the current regulatory value for
sulfites (10 ppm) takes into account the
potential for sensitive populations,
including infants and children, these
regulatory values are considered
protective, and no additional FQPA
safety factor is required.
E. Aggregate Risks and Determination of
Safety
In accordance with the FQPA, the
Agency must consider and aggregate
pesticide exposures and risks from three
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major sources: food, drinking water, and
residential exposures. There are no
residential uses of sulfur dioxide or
sodium metabisulfite, and exposures
through drinking water are not expected
based on the use pattern. Dietary
exposures resulting from the proposed
uses on blueberries are expected to be
below the 10 ppm FDA-established
regulatory level; therefore, there are no
dietary risks of concern from these uses
on blueberries.
Based on these risk assessments, EPA
concludes that there is a reasonable
certainty that no harm will result to the
general population, or to infants and
children from exposure to inorganic
sulfites resulting from the application of
sulfur dioxide and sodium
metabisulfite.
IV. Other Considerations
A. Analytical Enforcement Methodology
An adequate liquid chromatography
method with tandem mass spectrometry
detection (LC/MS/MS) method is
available for enforcing sulfite tolerances
in blueberries.
The method may be requested from:
Chief, Analytical Chemistry Branch,
Environmental Science Center, 701
Mapes Rd., Ft. Meade, MD 20755–5350;
telephone number: (410) 305–2905;
email address: residuemethods@
epa.gov.
B. International Residue Limits
In making its tolerance decisions, EPA
seeks to harmonize U.S. tolerances with
international standards whenever
possible, consistent with U.S. food
safety standards and agricultural
practices. EPA considers the
international maximum residue limits
(MRLs) established by the Codex
Alimentarius Commission (Codex), as
required by FFDCA section 408(b)(4).
There are no Codex MRLs for sulfur
dioxide in or on blueberry.
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V. Conclusion
Therefore, a tolerance is established
for residues of sulfur dioxide in or on
blueberry at 9 ppm. EPA is also
removing the expired time-limited
tolerance in paragraph (b) and reserving
paragraph (b) as a housekeeping
measure.
VI. 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,
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Jkt 259001
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), nor is it considered a
regulatory action under Executive Order
13771, entitled ‘‘Reducing Regulations
and Controlling Regulatory Costs’’ (82
FR 9339, February 3, 2017). This action
does not contain any information
collections subject to OMB approval
under the Paperwork Reduction Act
(PRA) (44 U.S.C. 3501 et seq.), nor does
it require any special considerations
under Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the 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
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consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: November 4, 2022.
Jennifer Saunders,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, for the reasons stated in the
preamble, EPA is amending 40 CFR
chapter I as follows:
PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
CHEMICAL RESIDUES IN FOOD
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.444:
a. Amend paragraph (a) by:
■ i. Designating the table as ‘‘Table 1 to
paragraph (a)’’.
■ ii. Adding in alphabetical order the
entry ‘‘Blueberry’’.
■ b. Removing and reserving paragraph
(b).
The addition reads as follows:
■
■
§ 180.444 Sulfur Dioxide; tolerances for
residues.
(a) * * *
TABLE 1 TO PARAGRAPH (a)
Parts per
million
Commodity
Blueberry ..............................
*
*
*
(b) [Reserved]
*
*
*
*
9
*
*
[FR Doc. 2022–25014 Filed 11–16–22; 8:45 am]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 87, Number 221 (Thursday, November 17, 2022)]
[Rules and Regulations]
[Pages 68909-68911]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-25014]
[[Page 68909]]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2021-0203; FRL-10212-01-OCSPP]
Sulfur Dioxide; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes a tolerance for residues of sulfur
dioxide in or on blueberry. Interregional Research Project Number 4
(IR-4) requested this tolerance under the Federal Food, Drug, and
Cosmetic Act (FFDCA).
DATES: This regulation is effective November 17, 2022. Objections and
requests for hearings must be received on or before January 17, 2023,
and must be filed in accordance with the instructions provided in 40
CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2021-0203, is available at
https://www.regulations.gov or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket) in the Environmental Protection
Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg.,
Rm. 3334, 1301 Constitution Ave. NW, Washington, DC 20460-0001. The
Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room and the OPP Docket is (202) 566-1744. For the latest
status information on EPA/DC services, docket access, visit https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Daniel Rosenblatt, Registration
Division (7505T), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-
0001; main telephone number: (202) 566-1030; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of EPA's
tolerance regulations at 40 CFR part 180 through the Office of the
Federal Register's e-CFR site at https://www.ecfr.gov/current/title-40.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, any person may file an
objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2021-0203 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
January 17, 2023. Addresses for mail and hand delivery of objections
and hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be 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-2021-0203, by one of
the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be CBI or other
information whose disclosure is restricted by statute.
Mail: OPP Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW, Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of June 28, 2021 (86 FR 33922) (FRL-10025-
08), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide petition (PP
0E8894) by IR-4, North Carolina State University, 1730 Varsity Drive,
Venture IV, Suite 210, Raleigh, NC 27606. The petition requested to
amend 40 CFR part 180 by establishing tolerances for residues of sulfur
dioxide, including its metabolite and degradates, in or on blueberry at
9 parts per million (ppm). That document referenced a summary of the
petition prepared by IR-4, the petitioner, which is available in the
docket, https://www.regulations.gov. Two comments were received on the
notice of filing from the United States Department of Agriculture and
the North American Blueberry Council. Both were in support of the
action.
III. Aggregate Risk Assessment and Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a
tolerance (the legal limit for a pesticide chemical residue in or on a
food) only if EPA determines that the tolerance is ``safe.'' Section
408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a
reasonable certainty that no harm will result from aggregate exposure
to the pesticide chemical residue, including all anticipated dietary
exposures and all other exposures for which there is reliable
information.'' This includes exposure through drinking water and in
residential settings but does not include occupational exposure.
Section 408(b)(2)(C) of FFDCA requires EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance and to ``ensure that there
is a reasonable certainty that no harm will result to infants and
children from aggregate exposure to the pesticide chemical residue.. .
.''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified in FFDCA section 408(b)(2)(D), EPA has reviewed the available
scientific data and other relevant information in support of this
action. EPA has sufficient data to assess the hazards of and to make a
determination on
[[Page 68910]]
aggregate exposure for sulfur dioxide including exposure resulting from
the tolerances established by this action. EPA's assessment of
exposures and risks associated with these inorganic sulfites follow.
A. Toxicological Profile
There is a large volume of published data detailing the toxicity of
sulfur dioxide and sodium metabisulfite, and consequently the toxicity
of these pesticides has been well established. Sodium metabisulfite
pads generate sulfur dioxide gas which then reacts with foods to
quickly form sulfite. In addition to the use of sodium metabisulfite
pads, direct application of sulfur dioxide gas is proposed for
blueberry treatments. For both treatments, sulfite is the residue of
concern in food and is determined by the analytical enforcement method.
EPA's Office of Air Quality Planning and Standards (OAQPS) has worked
extensively on sulfur dioxide, including setting national ambient air
quality standards (NAAQS) for sulfur dioxide, a gaseous air pollutant.
The U.S. Food and Drug Administration (FDA) has also performed an
extensive review of sulfiting agents (including sulfur dioxide, sodium
metabisulfite, and sodium bisulfite) that have been added to any food
or to any ingredient in any food. For the dietary assessment, EPA is
relying on the established FDA regulatory value for sulfite.
Sulfiting agents are used to add sulfites to foods and include
sulfur dioxide, sodium metabisulfite, sodium bisulfite, sodium sulfite,
potassium metabisulfite, and potassium bisulfite. Humans may experience
sensitivity reactions following exposure to sulfites including, but not
limited to, diarrhea, headache, difficulty breathing, vomiting and
nausea, and abdominal pain and cramps. Asthmatics account for many, but
not necessarily all, of the individuals who have a sensitivity to
sulfites. Given the known effects to certain individuals within the
population, the FDA requires that any food that contains a sulfiting
agent at >= 10 ppm or mg/kg be declared as such on the food label.
Additional information on the toxicological profile can be found at
https://www.regulations.gov in the document titled ``Inorganic
Sulfites. Human Health Risk Assessment in Support of a Section 3
Registration for Postharvest Fumigation of Blueberry'' (hereinafter
``Sulfur Dioxide Human Health Risk Assessment'') in docket ID number
EPA-HQ-OPP-2021-0203.
B. Toxicological Points of Departure/Levels of Concern
No appropriate toxicological endpoints were selected for sulfur
dioxide. The Agency is relying on the FDA-established regulatory level
of up to 10 ppm sulfite residues in foods.
C. Exposure Assessment
1. Dietary exposure from food and feed uses. In evaluating dietary
exposure to sulfur dioxide, EPA compared exposure from residues on
blueberries to the FDA-established regulatory level. EPA assessed
dietary exposures from these inorganic sulfites in food as follows:
Sulfite is the residue of concern for consumption of treated
blueberries. A quantitative dietary assessment was not conducted for
sulfite since no appropriate toxicological endpoints were selected. The
Agency is relying on the FDA-established regulatory level of up to 10
ppm sulfite residues in foods. Residues of sulfites in blueberry from
sulfur dioxide and sodium metabisulfite applications are expected to be
below the 10 ppm level when applied as tested in the blueberry residue
trials.
EPA did not use anticipated residue or PCT information in the
dietary assessment for sulfur dioxide.
2. Dietary exposure from drinking water. No residues are expected
in drinking water based on the current use pattern, which includes
post-harvest fumigant treatment in a chamber and slow release or dual
release pads that are placed in the clamshells used to distribute
blueberries.
3. From non-dietary exposure. The term ``residential exposure'' is
used in this document to refer to non-occupational, non-dietary
exposure (e.g., for lawn and garden pest control, indoor pest control,
termiticides, and flea and tick control on pets).
There are no uses of sulfur dioxide or sodium metabisulfite
resulting in direct residential exposures; therefore, residential
exposure is not expected.
4. 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.''
Unlike other pesticides for which EPA has followed a cumulative
risk approach based on a common mechanism of toxicity, EPA has not made
a common mechanism of toxicity finding as to the inorganic sulfites and
any other substances and the inorganic sulfites do not appear to
produce a toxic metabolite produced by other substances. For the
purposes of this tolerance action, therefore, EPA has not assumed that
the inorganic sulfites have a common mechanism of toxicity with other
substances.
D. Safety Factor for Infants and Children
1. In general. Section 408(b)(2)(C) of FFDCA provides that EPA
shall apply an additional tenfold (10X) margin of safety for infants
and children in the case of threshold effects to account for prenatal
and postnatal toxicity and the completeness of the database on toxicity
and exposure unless EPA determines based on reliable data that a
different margin of safety will be safe for infants and children. This
additional margin of safety is commonly referred to as the Food Quality
Protection Act Safety Factor (FQPA)(SF). In applying this provision,
EPA either retains the default value of 10X, or uses a different
additional safety factor when reliable data available to EPA support
the choice of a different factor.
Consistent with the factors specified in FFDCA section
408(b)(2)(D), EPA has also reviewed the available scientific data and
other relevant information in support of regulations establishing the
10 ppm maximum permissible level for residues of sulfur dioxide to
support a time-limited tolerance of sulfur dioxide residues in or on
fig (September 14, 2011; 76 FR 56644) (FRL-8887-2). EPA also considered
available information concerning the variability of the sensitivities
of major identifiable subgroups of consumers, including sulfite
sensitive individuals, infants, and children. EPA has concluded that
there is sufficient toxicological information for sulfur dioxide to
address risks to infants and children. In addition, the available
information indicated that there is no evidence of increased
quantitative or qualitative susceptibility of the offspring after in
utero or postnatal exposure. Based on the lack of observed
susceptibility, and since the current regulatory value for sulfites (10
ppm) takes into account the potential for sensitive populations,
including infants and children, these regulatory values are considered
protective, and no additional FQPA safety factor is required.
E. Aggregate Risks and Determination of Safety
In accordance with the FQPA, the Agency must consider and aggregate
pesticide exposures and risks from three
[[Page 68911]]
major sources: food, drinking water, and residential exposures. There
are no residential uses of sulfur dioxide or sodium metabisulfite, and
exposures through drinking water are not expected based on the use
pattern. Dietary exposures resulting from the proposed uses on
blueberries are expected to be below the 10 ppm FDA-established
regulatory level; therefore, there are no dietary risks of concern from
these uses on blueberries.
Based on these risk assessments, EPA concludes that there is a
reasonable certainty that no harm will result to the general
population, or to infants and children from exposure to inorganic
sulfites resulting from the application of sulfur dioxide and sodium
metabisulfite.
IV. Other Considerations
A. Analytical Enforcement Methodology
An adequate liquid chromatography method with tandem mass
spectrometry detection (LC/MS/MS) method is available for enforcing
sulfite tolerances in blueberries.
The method may be requested from: Chief, Analytical Chemistry
Branch, Environmental Science Center, 701 Mapes Rd., Ft. Meade, MD
20755-5350; telephone number: (410) 305-2905; email address:
[email protected].
B. International Residue Limits
In making its tolerance decisions, EPA seeks to harmonize U.S.
tolerances with international standards whenever possible, consistent
with U.S. food safety standards and agricultural practices. EPA
considers the international maximum residue limits (MRLs) established
by the Codex Alimentarius Commission (Codex), as required by FFDCA
section 408(b)(4).
There are no Codex MRLs for sulfur dioxide in or on blueberry.
V. Conclusion
Therefore, a tolerance is established for residues of sulfur
dioxide in or on blueberry at 9 ppm. EPA is also removing the expired
time-limited tolerance in paragraph (b) and reserving paragraph (b) as
a housekeeping measure.
VI. 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), nor is it considered a
regulatory action under Executive Order 13771, entitled ``Reducing
Regulations and Controlling Regulatory Costs'' (82 FR 9339, February 3,
2017). This action does not contain any information collections subject
to OMB approval under the Paperwork Reduction Act (PRA) (44 U.S.C. 3501
et seq.), nor does it require any special considerations under
Executive Order 12898, entitled ``Federal Actions to Address
Environmental Justice in Minority Populations and Low-Income
Populations'' (59 FR 7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the 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).
VII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: November 4, 2022.
Jennifer Saunders,
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. 180.444:
0
a. Amend paragraph (a) by:
0
i. Designating the table as ``Table 1 to paragraph (a)''.
0
ii. Adding in alphabetical order the entry ``Blueberry''.
0
b. Removing and reserving paragraph (b).
The addition reads as follows:
Sec. 180.444 Sulfur Dioxide; tolerances for residues.
(a) * * *
Table 1 to Paragraph (a)
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
Blueberry............................................... 9
* * * * *
------------------------------------------------------------------------
(b) [Reserved]
* * * * *
[FR Doc. 2022-25014 Filed 11-16-22; 8:45 am]
BILLING CODE 6560-50-P