Potassium Salts of Hops Beta Acids; Exemption From the Requirement of a Tolerance, 63680-63683 [2015-26600]
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63680
Federal Register / Vol. 80, No. 203 / Wednesday, October 21, 2015 / Rules and Regulations
§ 165.T13–290 Safety Zone; 520 Bridge,
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(a) Location: The following area is
designated as a safety zone: All waters
within 100 yards of the east span of the
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(b) Regulations: In accordance with
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brought any vessel into the safety zone
without permission of the Captain of the
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Captain of the Port by contacting the
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(c) Dates: This rule is effective from
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Dated: September 30, 2015.
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requests for hearings must be received
on or before December 21, 2015, 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–2014–0374, 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. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
ENVIRONMENTAL PROTECTION
AGENCY
Robert McNally, Biopesticides and
Pollution Prevention Division (7511P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
DC 20460–0001; main telephone
number: (703) 305–7090; email address:
BPPDFRNotices@epa.gov.
40 CFR Part 180
SUPPLEMENTARY INFORMATION:
[EPA–HQ–OPP–2014–0374; FRL–9933–73]
I. General Information
Potassium Salts of Hops Beta Acids;
Exemption From the Requirement of a
Tolerance
A. Does this Action apply to me?
[FR Doc. 2015–26754 Filed 10–20–15; 8:45 am]
BILLING CODE 9110–04P
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes an
exemption from the requirement of a
tolerance for residues of the biochemical
pesticide potassium salts of hops beta
acids in or on honey and honeycomb for
the control of Varroa mites in
accordance with label directions and
good agricultural practices. Interregional
Research Project Number 4, on behalf of
Beta Tec Hop Products, 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 potassium salts of hops
beta acids in or on honey and
honeycomb.
DATES: This regulation is effective
October 21, 2015. Objections and
tkelley on DSK3SPTVN1PROD with RULES
SUMMARY:
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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 Government Printing
Office’s e-CFR site at https://www.ecfr.
gov/cgi-bin/text-idx?&c=ecfr&tpl=/
ecfrbrowse/Title40/40tab_02.tpl.
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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–2014–0374 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 December 21, 2015. 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–
2014–0374, 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 September
5, 2014 (79 FR 53009) (FRL–9914–98),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide tolerance petition (PP 3E8217)
by Interregional Research Project
Number 4, 500 College Road East, Suite
201W, Princeton, NJ 08540, on behalf of
BetaTec Hop Products, Inc. (the
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tkelley on DSK3SPTVN1PROD with RULES
petitioner). The petition requested that
40 CFR part 180 be amended by
establishing an exemption from the
requirement of a tolerance for residues
of potassium salts of hop beta acids (K–
HBAs) in or on honey and honeycomb
resulting from the control of Varroa
mites. That document referenced a
summary of the petition prepared by the
petitioner, which is available in the
docket, https://www.regulations.gov.
There were 63 comments received in
response to the batched notice of filing
but none were relevant to the
establishment of a tolerance for
potassium salts of hops beta acids.
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 require 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. . . .’’ Additionally,
EPA is required to take into account the
factors set forth in FFDCA section
408(b)(2)(D).
EPA performs a number of analyses to
determine the risks from aggregate
exposure to pesticide residues. First,
EPA determines the toxicity of
pesticides. Second, EPA examines
exposure to the pesticide through food,
drinking water, and through other
exposures that occur as a result of
pesticide use in residential settings.
III. Toxicological Profile
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
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available information concerning the
variability of the sensitivities of major
identifiable subgroups of consumers,
including infants and children.
A. Overview of Potassium Salts of Hops
Beta Acids
K–HBAs are derived from the resin
components of the cones of female hop
plants Humulus lupulus. The three
major components of K–HBAs are
Lupulone (30–55% with an isopropyl
side chain), Colupulone (20–55% with
an isobutyl side chain), and Adlupulone
(5–10% with a secbutyl side chain); the
components differ only in the R-side
chain attached. K–HBA is classified as
a biochemical pesticide because it is
naturally occurring (found in Humulus
lupulus plant), has a non-toxic mode of
action against the target pest, and has a
history of exposure to humans and the
environment demonstrating minimal
toxicity. There is a long history of safe
use of HBAs via the oral and dietary
exposure to humans from its use as a
preservative on meats (estimated range
4.4 milligrams/kilograms (mg/kg) of
cooked meat—5.5 mg/kg of frankfurter)
and its presence in the beer brewing
process. Due to its long history of
exposure, K–HBAs are considered to be
generally recognized as safe (GRAS) by
FDA.
B. Biochemical Pesticide Toxicology
Data Requirements
All applicable mammalian toxicology
data requirements supporting the
petition to establish an exemption from
the requirement of a tolerance for the
use of potassium salts of hops beta acids
as an active ingredient for use to control
Varroa mites in or on honey and
honeycomb have been fulfilled. No
significant toxicological effects were
observed in the acute toxicity study or
other information from the literature
that was used to address the toxicity
data requirements. For the Tier I
subchronic toxicity studies, data and
information from scientific literature
were used in support of acceptable
rationales to address the data
requirements, focusing on the long
history of exposure to K–HBAs in food
preservation and in the production of
beer, which is commonly consumed in
the United States. K–HBAs are not
structurally-related to known mutagens,
nor are they in a chemical class known
to contain a known mutagen. Further,
from the available toxicity information,
there were no systemic effects of
potassium salts of hops beta acids via
the oral, dermal, or inhalation routes of
exposure. For a summary of the data
upon which EPA relied, and its human
health risk assessment based on that
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data, please refer to the document
entitled, ‘‘Federal Food, Drug, and
Cosmetic Act (FFDCA) Considerations
for Potassium Salts of Hops Beta acids’’
(July 15, 2015), available in the docket
for this action.
IV. Aggregate Exposures
In examining aggregate exposure,
FFDCA section 408 directs EPA to
consider available information
concerning exposures from the pesticide
residue in food and all other nonoccupational exposures, including
drinking water from ground water or
surface water and exposure through
pesticide use in gardens, lawns, or
buildings (residential and other indoor
uses).
A. Dietary Exposure
Human dietary exposure through food
to residues of K–HBAs already occurs
via its use as a preservative in meats and
its natural presence in beer brewing
production. EPA does not expect much
residue of potassium salts of hops beta
acids in honey from its use as a
pesticide in hives based on residue
studies. In three different studies
conducted over 3 years, only one honey
sample from one honey super was
shown to have residues of hops beta
acids (0.44 part per million (ppm)), and
the residue level was only slightly above
the analytical limits of detection (0.41
ppm) and well below the Limit of
Quantitation (1.2 ppm).
No significant exposure via drinking
water is expected from its use as an
active ingredient as a pesticide. K–HBAs
are non-volatile and are expected to
degrade rapidly, with 100% degradation
in 36 hours in the light and 4 days in
the dark. Furthermore, as an insecticide,
K–HBAs are formulated into a viscous
liquid and coated on fiber strips which
are placed inside the beehive such that
the product is not sprayed or applied in
any way that it would be expected to
contact any source of drinking water.
Should exposure occur, however,
minimal to no risk is expected for the
general population, including infants
and children, due to the long history of
dietary exposure to K–HBAs.
B. Other Non-Occupational Exposure
Non-occupational exposure to
potasium salts of hops beta acids is not
expected because potassium salts of
hops beta acids is formulated into a
viscous liquid and coated on fiber strips
which are placed inside the beehive.
There are no residential proposed uses.
However, minimal to no risk is expected
for the general population, including
infants and children, due to the minimal
toxicity of this chemical as
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demonstrated in the data submitted and
evaluated by the Agency, as fully
explained in the document entitled,
‘‘Federal Food, Drug, and Cosmetic Act
(FFDCA) Considerations for Potassium
Salts of Hops Beta acids’’ (July 15,
2015), available in the docket for this
action.
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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 potassium salts of
hops beta acids to share a common
mechanism of toxicity with any other
substances, and potassium salts of hops
beta acids does not appear to produce a
toxic metabolite produced by other
substances. For the purposes of this
tolerance action, therefore, EPA has
assumed that potassium salts of hops
beta acids 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 Web site at https://www.epa.
gov/pesticides/cumulative.
VI. Determination of Safety for U.S.
Population, Infants and Children
FFDCA section 408(b)(2)(C) provides
that, in considering the establishment of
a tolerance or tolerance exemption for a
pesticide chemical residue, EPA shall
assess the available information about
consumption patterns among infants
and children, special susceptibility of
infants and children to pesticide
chemical residues, and the cumulative
effects on infants and children of the
residues and other substances with a
common mechanism of toxicity. In
addition, FFDCA section 408(b)(2)(C)
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
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 (FQPA) Safety Factor. In
applying this provision, EPA either
retains the default value of 10X, or uses
a different additional or no safety factor
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when reliable data are available to
support a different additional or no
safety factor.
As part of its qualitative assessment,
EPA evaluated the available toxicity and
exposure data on potassium salts of
hops beta acids and considered its
validity, completeness, and reliability,
as well as the relationship of this
information to human risk. EPA
considers the toxicity database to be
complete and has identified no residual
uncertainty with regard to prenatal and
postnatal toxicity or exposure. No
hazard was identified based on the
available studies; therefore, EPA
concludes that there are no threshold
effects of concern to infants, children, or
adults from potassium salts of hops beta
acids. As a result, EPA concludes that
no additional margin of exposure
(safety) is necessary.
VII. Analytical Enforcement
Methodology
An analytical method is not required
for enforcement purposes because EPA
is establishing an exemption from the
requirement of a tolerance without any
numerical limitation.
VIII. Conclusion
Based on its assessment of potassium
salts of hops beta acids, EPA concludes
that there is a reasonable certainty that
no harm will result to the general
population, or to infants and children,
from aggregate exposure to potassium
salts of hops beta acids. EPA is therefore
establishing an exemption from the
requirement of a tolerance for residues
of potassium salts of hops beta acids for
the control of Varroa mites in or on
honey and honeycomb, in accordance
with label directions and good
agricultural practices.
IX. Statutory and Executive Order
Reviews
This final rule establishes an
exemption from the requirement of 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 final rule has been exempted from
review under Executive Order 12866,
this final rule 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
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Risks’’ (62 FR 19885, April 23, 1997).
This final rule 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 exemption 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 final rule 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 final rule. In addition, this final
rule does not impose any enforceable
duty or contain any unfunded mandate
as described under Title II of the
Unfunded Mandates Reform Act of 1995
(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 of 1995
(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).
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Federal Register / Vol. 80, No. 203 / Wednesday, October 21, 2015 / Rules and Regulations
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: September 29, 2015.
Jack E. Housenger,
Director, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Add section 180.1333 to subpart D
to read as follows:
■
§ 180.1333 Potassium Salts of Hops Beta
acids; exemption from the requirement of a
tolerance.
An exemption from the requirement
of a tolerance is established for residues
of the biochemical potassium salts of
hops beta acids in or on honey and
honeycomb, when used for the control
of Varroa mites in accordance with label
directions and good agricultural
practices.
[FR Doc. 2015–26600 Filed 10–20–15; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
1-yl]-w-[[(9Z)-1-oxo-9-octadecen1yl]oxy]- on food or feed commodities.
DATES: This regulation is effective
October 21, 2015. Objections and
requests for hearings must be received
on or before December 21, 2015, 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–2015–0442, 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. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Susan Lewis, 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:
[EPA–HQ–OPP–2015–0442; FRL–9935–34]
I. General Information
Poly[oxy(methyl-1,2-ethanediyl)], α[(9Z)-1-oxo-9-octadecen-1-yl]-w-[[(9Z)1-oxo-9-octadecen-1yl]oxy]-;
Exemption From the Requirement of a
Tolerance
A. Does this action apply to me?
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes an
exemption from the requirement of a
tolerance for residues of
poly[oxy(methyl-1,2-ethanediyl)], a[(9Z)-1-oxo-9-octadecen-1-yl]-w-[[(9Z)-1oxo-9-octadecen-1yl]oxy]- (CAS Reg.
No. 26571–49–3) 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(methyl-1,2ethanediyl)], a-[(9Z)-1-oxo-9-octadecen-
tkelley on DSK3SPTVN1PROD with RULES
SUMMARY:
VerDate Sep<11>2014
16:24 Oct 20, 2015
Jkt 238001
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 Government Printing
Office’s e-CFR site at https://www.ecfr.
PO 00000
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Fmt 4700
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63683
gov/cgi-bin/text-idx?&c=ecfr&tpl=/
ecfrbrowse/Title40/40tab_02.tpl.
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–2015–0442 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 December 21, 2015. 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–
2015–0442, 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 August 26,
2015 (80 FR 51759) (FRL–9931–74),
EPA issued a document pursuant to
FFDCA section 408, 21 U.S.C. 346a,
announcing the receipt of a pesticide
petition (PP) IN–10826 filed by BYK
USA Inc., 524 South Cherry Street,
Wallingford, CT 06492–4453. The
E:\FR\FM\21OCR1.SGM
21OCR1
Agencies
[Federal Register Volume 80, Number 203 (Wednesday, October 21, 2015)]
[Rules and Regulations]
[Pages 63680-63683]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-26600]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2014-0374; FRL-9933-73]
Potassium Salts of Hops Beta Acids; Exemption From the
Requirement of a Tolerance
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 the biochemical pesticide potassium
salts of hops beta acids in or on honey and honeycomb for the control
of Varroa mites in accordance with label directions and good
agricultural practices. Interregional Research Project Number 4, on
behalf of Beta Tec Hop Products, 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 potassium salts of hops beta acids in or on honey and
honeycomb.
DATES: This regulation is effective October 21, 2015. Objections and
requests for hearings must be received on or before December 21, 2015,
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-2014-0374, 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. Please review the visitor instructions and
additional information about the docket available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Robert McNally, Biopesticides and
Pollution Prevention Division (7511P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460-0001; main telephone number: (703) 305-7090; email
address: BPPDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
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 Government Printing Office's e-CFR site at https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
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-2014-0374 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
December 21, 2015. 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-2014-0374, 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 September 5, 2014 (79 FR 53009) (FRL-
9914-98), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide tolerance
petition (PP 3E8217) by Interregional Research Project Number 4, 500
College Road East, Suite 201W, Princeton, NJ 08540, on behalf of
BetaTec Hop Products, Inc. (the
[[Page 63681]]
petitioner). The petition requested that 40 CFR part 180 be amended by
establishing an exemption from the requirement of a tolerance for
residues of potassium salts of hop beta acids (K-HBAs) in or on honey
and honeycomb resulting from the control of Varroa mites. That document
referenced a summary of the petition prepared by the petitioner, which
is available in the docket, https://www.regulations.gov. There were 63
comments received in response to the batched notice of filing but none
were relevant to the establishment of a tolerance for potassium salts
of hops beta acids.
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 require 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. . .
.'' Additionally, EPA is required to take into account the factors set
forth in FFDCA section 408(b)(2)(D).
EPA performs a number of analyses to determine the risks from
aggregate exposure to pesticide residues. First, EPA determines the
toxicity of pesticides. Second, EPA examines exposure to the pesticide
through food, drinking water, and through other exposures that occur as
a result of pesticide use in residential settings.
III. Toxicological Profile
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.
A. Overview of Potassium Salts of Hops Beta Acids
K-HBAs are derived from the resin components of the cones of female
hop plants Humulus lupulus. The three major components of K-HBAs are
Lupulone (30-55% with an isopropyl side chain), Colupulone (20-55% with
an isobutyl side chain), and Adlupulone (5-10% with a secbutyl side
chain); the components differ only in the R-side chain attached. K-HBA
is classified as a biochemical pesticide because it is naturally
occurring (found in Humulus lupulus plant), has a non-toxic mode of
action against the target pest, and has a history of exposure to humans
and the environment demonstrating minimal toxicity. There is a long
history of safe use of HBAs via the oral and dietary exposure to humans
from its use as a preservative on meats (estimated range 4.4
milligrams/kilograms (mg/kg) of cooked meat--5.5 mg/kg of frankfurter)
and its presence in the beer brewing process. Due to its long history
of exposure, K-HBAs are considered to be generally recognized as safe
(GRAS) by FDA.
B. Biochemical Pesticide Toxicology Data Requirements
All applicable mammalian toxicology data requirements supporting
the petition to establish an exemption from the requirement of a
tolerance for the use of potassium salts of hops beta acids as an
active ingredient for use to control Varroa mites in or on honey and
honeycomb have been fulfilled. No significant toxicological effects
were observed in the acute toxicity study or other information from the
literature that was used to address the toxicity data requirements. For
the Tier I subchronic toxicity studies, data and information from
scientific literature were used in support of acceptable rationales to
address the data requirements, focusing on the long history of exposure
to K-HBAs in food preservation and in the production of beer, which is
commonly consumed in the United States. K-HBAs are not structurally-
related to known mutagens, nor are they in a chemical class known to
contain a known mutagen. Further, from the available toxicity
information, there were no systemic effects of potassium salts of hops
beta acids via the oral, dermal, or inhalation routes of exposure. For
a summary of the data upon which EPA relied, and its human health risk
assessment based on that data, please refer to the document entitled,
``Federal Food, Drug, and Cosmetic Act (FFDCA) Considerations for
Potassium Salts of Hops Beta acids'' (July 15, 2015), available in the
docket for this action.
IV. Aggregate Exposures
In examining aggregate exposure, FFDCA section 408 directs EPA to
consider available information concerning exposures from the pesticide
residue in food and all other non-occupational exposures, including
drinking water from ground water or surface water and exposure through
pesticide use in gardens, lawns, or buildings (residential and other
indoor uses).
A. Dietary Exposure
Human dietary exposure through food to residues of K-HBAs already
occurs via its use as a preservative in meats and its natural presence
in beer brewing production. EPA does not expect much residue of
potassium salts of hops beta acids in honey from its use as a pesticide
in hives based on residue studies. In three different studies conducted
over 3 years, only one honey sample from one honey super was shown to
have residues of hops beta acids (0.44 part per million (ppm)), and the
residue level was only slightly above the analytical limits of
detection (0.41 ppm) and well below the Limit of Quantitation (1.2
ppm).
No significant exposure via drinking water is expected from its use
as an active ingredient as a pesticide. K-HBAs are non-volatile and are
expected to degrade rapidly, with 100% degradation in 36 hours in the
light and 4 days in the dark. Furthermore, as an insecticide, K-HBAs
are formulated into a viscous liquid and coated on fiber strips which
are placed inside the beehive such that the product is not sprayed or
applied in any way that it would be expected to contact any source of
drinking water.
Should exposure occur, however, minimal to no risk is expected for
the general population, including infants and children, due to the long
history of dietary exposure to K-HBAs.
B. Other Non-Occupational Exposure
Non-occupational exposure to potasium salts of hops beta acids is
not expected because potassium salts of hops beta acids is formulated
into a viscous liquid and coated on fiber strips which are placed
inside the beehive. There are no residential proposed uses. However,
minimal to no risk is expected for the general population, including
infants and children, due to the minimal toxicity of this chemical as
[[Page 63682]]
demonstrated in the data submitted and evaluated by the Agency, as
fully explained in the document entitled, ``Federal Food, Drug, and
Cosmetic Act (FFDCA) Considerations for Potassium Salts of Hops Beta
acids'' (July 15, 2015), available in the docket for this action.
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 potassium salts of hops beta acids to share a
common mechanism of toxicity with any other substances, and potassium
salts of hops beta acids does not appear to produce a toxic metabolite
produced by other substances. For the purposes of this tolerance
action, therefore, EPA has assumed that potassium salts of hops beta
acids 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 Web site at https://www.epa.gov/pesticides/cumulative.
VI. Determination of Safety for U.S. Population, Infants and Children
FFDCA section 408(b)(2)(C) provides that, in considering the
establishment of a tolerance or tolerance exemption for a pesticide
chemical residue, EPA shall assess the available information about
consumption patterns among infants and children, special susceptibility
of infants and children to pesticide chemical residues, and the
cumulative effects on infants and children of the residues and other
substances with a common mechanism of toxicity. In addition, FFDCA
section 408(b)(2)(C) 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 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 (FQPA) Safety Factor. In applying
this provision, EPA either retains the default value of 10X, or uses a
different additional or no safety factor when reliable data are
available to support a different additional or no safety factor.
As part of its qualitative assessment, EPA evaluated the available
toxicity and exposure data on potassium salts of hops beta acids and
considered its validity, completeness, and reliability, as well as the
relationship of this information to human risk. EPA considers the
toxicity database to be complete and has identified no residual
uncertainty with regard to prenatal and postnatal toxicity or exposure.
No hazard was identified based on the available studies; therefore, EPA
concludes that there are no threshold effects of concern to infants,
children, or adults from potassium salts of hops beta acids. As a
result, EPA concludes that no additional margin of exposure (safety) is
necessary.
VII. Analytical Enforcement Methodology
An analytical method is not required for enforcement purposes
because EPA is establishing an exemption from the requirement of a
tolerance without any numerical limitation.
VIII. Conclusion
Based on its assessment of potassium salts of hops beta acids, EPA
concludes that there is a reasonable certainty that no harm will result
to the general population, or to infants and children, from aggregate
exposure to potassium salts of hops beta acids. EPA is therefore
establishing an exemption from the requirement of a tolerance for
residues of potassium salts of hops beta acids for the control of
Varroa mites in or on honey and honeycomb, in accordance with label
directions and good agricultural practices.
IX. Statutory and Executive Order Reviews
This final rule establishes an exemption from the requirement of 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 final rule has been exempted from review
under Executive Order 12866, this final rule 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 final rule 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 exemption 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 final rule 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 final rule. In addition,
this final rule does not impose any enforceable duty or contain any
unfunded mandate as described under Title II of the Unfunded Mandates
Reform Act of 1995 (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 of 1995 (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).
[[Page 63683]]
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: September 29, 2015.
Jack E. Housenger,
Director, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
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. Add section 180.1333 to subpart D to read as follows:
Sec. 180.1333 Potassium Salts of Hops Beta acids; exemption from the
requirement of a tolerance.
An exemption from the requirement of a tolerance is established for
residues of the biochemical potassium salts of hops beta acids in or on
honey and honeycomb, when used for the control of Varroa mites in
accordance with label directions and good agricultural practices.
[FR Doc. 2015-26600 Filed 10-20-15; 8:45 am]
BILLING CODE 6560-50-P