Benoxacor; Partial Grant and Partial Denial of Petition, and Amendment of Tolerance to Include S-Metolachlor, 21628-21631 [05-8119]
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Federal Register / Vol. 70, No. 80 / Wednesday, April 27, 2005 / Rules and Regulations
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[FR Doc. 05–8437 Filed 4–26–05; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[OPP–2005–0080; FRL–7709–2]
Benoxacor; Partial Grant and Partial
Denial of Petition, and Amendment of
Tolerance to Include S-Metolachlor
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: EPA is granting, in part, and
denying, in part, pesticide petition
7E3489 submitted by Syngenta Crop
Protection, Inc., and is amending the
tolerance for benoxacor at 40 CFR
180.460 to include a reference to Smetolachlor, in addition to the existing
reference to metolachlor. EPA issued a
notice pursuant to section 408(d)(3) of
FFDCA, 21 U.S.C. 346a(d)(3) in the
Federal Register of August 3, 2003 (68
FR 46620) (FRL–7317–6) announcing
the filing of a petition requesting that
the tolerance expression for the inert
ingredient benoxacor (safener) in 40
CFR 180.460 be amended to remove
references to metolachlor and replace it
with references to S-metoloachlor.
Although EPA finds it is safe to add a
reference to S-metolachlor to this
tolerance regulation, EPA does not agree
that grounds exist to remove the
reference to metolachlor. Thus, EPA is
granting Syngenta’s petition in as far as
it seeks to add the reference to Smetolachlor but is denying the request
to remove metolachlor.
DATES: This regulation is effective April
27, 2005. Objections and requests for
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hearings must be received on or before
June 27, 2005.
ADDRESSES: To submit a written
objection or hearing request, follow the
detailed instructions as provided in
Unit VIII. of the SUPPLEMENTARY
INFORMATION. EPA has established a
docket for this action under Docket
identification (ID) number OPP–2005–
0080. All documents in the docket are
listed in the EDOCKET index at http:/
/www.epa.gov/edocket. Although listed
in the index, some information is not
publicly available, i.e., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the Internet and will be
publicly available only in hard copy
form. Publicly available docket
materials are available either
electronically in EDOCKET or in hard
copy at the Public Information and
Records Integrity Branch (PIRIB), Rm.
119, Crystal Mall #2, 1801 S. Bell St.,
Arlington, VA. This docket facility is
open from 8:30 a.m. to 4 p.m., Monday
through Friday, excluding legal
holidays. The docket telephone number
is (703) 305–5805.
FOR FURTHER INFORMATION CONTACT:
Karen Angulo, Registration Division
(7505C), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave, NW., Washington,
DC 20460–0001; telephone number:
(703) 306–0404; e-mail address:
angulo.karen@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. Potentially
affected entities may include, but are
not limited to:
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• Crop production (NAICS code 111)
• Animal production (NAICS code
112)
• Food manufacturing (NAICS code
311)
• Pesticide manufacturing (NAICS
code 32532)
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
assist you and others in determining
whether this action might apply to
certain entities. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
B. How Can I Access Electronic Copies
of this Document and Other Related
Information?
In addition to using EDOCKET (http:/
/www.epa.gov/edocket/), you may
access this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr/. A
frequently updated electronic version of
40 CFR part 180 is available at E-CFR
Beta Site Two at https://
www.gpoaccess.gov/ecfr/.
II. Background and Statutory Findings
In the Federal Register of August 6,
2003 (68 FR 46620) (FRL–7317–6), EPA
issued a notice pursuant to section
408(d)(3) of FFDCA, 21 U.S.C.
346a(d)(3), announcing the filing of
pesticide petition (7E3489) by Syngenta
Crop Protection, Inc., P.O. Box 18300,
Greensboro, NC 27419–8300. The
petition requested that the tolerance
expression for the inert ingredient
benoxacor (safener) in 40 CFR 180.460
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Federal Register / Vol. 70, No. 80 / Wednesday, April 27, 2005 / Rules and Regulations
be amended to remove the references to
metolachlor and replace it with
references to S-metolachlor. Currently,
the benoxacor tolerance permits
residues of benoxacor in or on raw
agricultural commodities for which
tolerances have been established for the
herbicide metolachlor when benoxacor
is used in pesticide formulations
containing metolachlor. Syngenta’s
petition seeks this amendment because
it has voluntarily canceled all its
metolachlor product registrations,
including its metolachlor registrations
containing the safener benoxacor, and
has registered products containing Smetolachlor in their place. Some or all
of these new registrations contain not
only S-metolachlor but benoxacor as
well.
The notice of filing included a
summary of Syngenta’s petition. EPA
received one comment, which is
discussed further in Unit IV.
This final rule is issued pursuant to
section 408(d) of FFDCA, as amended
by the FQPA (21 U.S.C. 346a(d)).
Section 408 of FFDCA authorizes the
establishment of tolerances, exemptions
from the requirement of a tolerance,
modifications in tolerances, and
revocation of tolerances for residues of
pesticide chemicals in or on raw
agricultural commodities and processed
foods. Without a tolerance or tolerance
exemption, food containing pesticide
residues is considered to be unsafe and
therefore ‘‘adulterated’’ under section
402(a) of the FFDCA. If food containing
pesticide residues is found to be
adulterated, the food may not be
distributed in interstate commerce (21
U.S.C. 331(a) and 342 (a)).
III. What Action is the Agency Taking?
In this action, EPA is ruling on a
petition (7E3489) filed by Syngenta
Crop Protection pursuant to FFDCA
section 408(d) to amend a tolerance
regulation. Section 408(d)(4) authorizes
EPA to act on a petition by issuing a
final rule adopting the amendment
sought by the petition, issuing a final
rule that varies from the amendment
sought by the petition, or completely
denying the petition. For the reasons
described below, EPA has chosen the
middle course with regard to Syngenta’s
petition - granting it only in part and
denying the remainder.
The Agency is granting Syngenta’s
petition in part. The Agency has
determined that the tolerance for
benoxacor at 40 CFR 180.460 should be
amended to include a reference to both
metolachlor and S-metolachlor. EPA
agrees there are sufficient grounds to
amend the tolerance expression for
benoxacor to include a reference to S-
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metolachlor, the product Syngenta is
now marketing in place of the
metolachlor registrations it has
voluntarily canceled. EPA has
previously determined that the existing
benoxacor tolerances meet the safety
standard of FFDCA section
408(b)(2)(A)(i). See the Federal Register
of February 13, 1998, (63 FR 7299)
(FRL–5771–1).
A chronic dietary exposure and risk
assessment was conducted using Dietary
Exposure Evaluation Model-Food
Commodity Intake Database (DEEMFCIDTM), which uses food consumption
data from the United States Department
of Agriculture’s (USDA’s) Continuing
Surveys of Food Intakes by Individuals
(CSFII) from 1994–1996 and 1998. The
chronic analysis assumes tolerance-level
residues on all crops with established,
pending, or proposed tolerances for
metolachlor and/or S-metolachlor. The
analysis also assumes that 100% of the
crops included in the assessment were
treated with metolachlor and/or Smetolachlor and its safener, benoxacor.
These assumptions result in over
estimates of exposure and are, therefore,
highly conservative with respect to
dietary risk assessment. Even with these
assumptions, the dietary risk estimates
for all population subgroups are less
than 15% of the chronic PopulationAdjusted Dose (cPAD). Generally EPA is
concerned when risk estimates exceed
100% of the cPAD. Therefore, the
dietary risk estimates are below EPA’s
level of concern for all population
subgroups, including those of infants
and children. There are no acute
toxicological or cancer concerns for
benoxacor.
Accordingly, EPA finds for the
reasons set forth in the Federal Register
notice of February 13, 1998 (63 FR
7299), establishing the existing
benoxacor tolerances, that these
tolerances, as amended today, are safe
for the general population, including
infants and children, within the
meaning of FFDCA section
408(b)(2)(A)(i).
EPA does not agree, however, that
grounds exist to remove the reference to
metolachlor in 40 CFR 180.460 as
requested by the petition. As noted, EPA
has found previously that residues of
benoxacor resulting from its use with
metolachlor, are safe and will be safe
under the regulation when amended to
also reference S-metolachlor. Further,
while Syngenta may have canceled its
metolachlor registrations, there are
existing metolachlor registrations
currently held by other persons. The
fact that one registrant of several has
chosen to stop marketing the pesticide
does not constitute the ‘‘abandonment’’
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of a pesticide as contemplated by 40
CFR 180.32(b) that would justify the
administrative amendment or repeal of
a tolerance. Further, as the commenter
has made clear, existing metolachlor
registrants are interested in retaining the
reference to metolachlor in the
benoxacor tolerance expression. For
these reasons, EPA is denying
Syngenta’s request to remove
metolachlor from the existing tolerance
expression.
Based on its decision to grant, in part,
and deny, in part, Syngenta’s petition,
EPA is today amending the tolerance
expression for benoxacor at 40 CFR
180.460(a) as found in the regulatory
section of this document.
IV. Public Comments
As noted in Unit.II. of this document,
EPA received a comment objecting to
Syngenta’s petition to replace the
references to metolachlor in 40 CFR
180.460 with references to Smetolachlor. Specifically, the
commenter argues that the proposed
amendment is unnecessary to protect
public health; that it would establish an
inappropriate precedent prior to the
adoption of an isomer active ingredient
policy; and that the rationale for action
that Syngenta has offered is materially
incomplete and inadequate. Because
EPA has decided for reasons set forth in
Unit.III. of this document to retain the
references to metolachlor in 40 CFR
180.460, EPA need not reach the
commenter’s arguments objecting to
Syngenta’s proposed deletion of
metolachlor from that regulation. The
commenter also argues, however, that as
a general matter Syngenta’s petition
provides no pertinent new ‘‘data,
information and arguments’’ or
‘‘reasonable grounds’’ in support of the
petition. EPA disagrees with this
comment to the extent it suggests there
are inadequate grounds for adding
references to S-metolachlor to the
tolerance expression at 40 CFR 180.460.
As discussed above, the petition noted
that EPA has previously found that
benoxacor residues are safe and has
determined that this action will not alter
the assumptions upon which that
determination relied. Accordingly, EPA
believes reasonable grounds exist to add
references to S-metolachlor to 40 CFR
180.460.
V. Objections and Hearing Requests
Under section 408(g) of the FFDCA, as
amended by the FQPA, any person may
file an objection to any aspect of this
regulation and may also request a
hearing on those objections. The EPA
procedural regulations which govern the
submission of objections and requests
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Federal Register / Vol. 70, No. 80 / Wednesday, April 27, 2005 / Rules and Regulations
for hearings appear in 40 CFR part 178.
Although the procedures in those
regulations require some modification to
reflect the amendments made to the
FFDCA by the FQPA of 1996, EPA will
continue to use those procedures, with
appropriate adjustments, until the
necessary modifications can be made.
The new section 408(g) provides
essentially the same process for persons
to ‘‘object’’ to a regulation for an
exemption from the requirement of a
tolerance issued by EPA under new
section 408(d), as was provided in the
old FFDCA sections 408 and 409.
However, the period for filing objections
is now 60 days, rather than 30 days.
A. What Do I Need to Do to File an
Objection or Request a Hearing?
You must file your objection or
request a hearing on this regulation in
accordance with the instructions
provided in this unit and in 40 CFR part
178. To ensure proper receipt by EPA,
you must identify docket ID number
OPP–2005–0080 in the subject line on
the first page of your submission. All
requests must be in writing, and must be
mailed or delivered to the Hearing Clerk
on or before June 27, 2005.
1. Filing the request. Your objection
must specify the specific provisions in
the regulation that you object to, and the
grounds for the objections (40 CFR
178.25). If a hearing is requested, the
objections must include a statement of
the factual issues(s) on which a hearing
is requested, the requestor’s contentions
on such issues, and a summary of any
evidence relied upon by the objector (40
CFR 178.27). Information submitted in
connection with an objection or hearing
request may be claimed confidential by
marking any part or all of that
information as CBI. Information so
marked will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2. A copy of the
information that does not contain CBI
must be submitted for inclusion in the
public record. Information not marked
confidential may be disclosed publicly
by EPA without prior notice.
Mail your written request to: Office of
the Hearing Clerk (1900L),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001. You may also deliver
your request to the Office of the Hearing
Clerk in Suite 350, 1099 14th St., NW.,
Washington, DC 20005. The Office of
the Hearing Clerk is open from 8 a.m.
to 4 p.m., Monday through Friday,
excluding legal holidays. The telephone
number for the Office of the Hearing
Clerk is (202) 564–6255.
2. Copies for the Docket. In addition
to filing an objection or hearing request
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with the Hearing Clerk as described in
Unit VIII.A., you should also send a
copy of your request to the PIRIB for its
inclusion in the official record that is
described in ADDRESSES. Mail your
copies, identified by docket ID number
OPP–2005–0080, to: Public Information
and Records Integrity Branch,
Information Resources and Services
Division (7502C), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460. In person or by
courier, bring a copy to the location of
the PIRIB described in ADDRESSES. You
may also send an electronic copy of
your request via e-mail to: oppdocket@epa.gov. Please use an ASCII
file format and avoid the use of special
characters and any form of encryption.
Copies of electronic objections and
hearing requests will also be accepted
on disks in WordPerfect 6.1/8.0 or
ASCII file format. Do not include any
CBI in your electronic copy. You may
also submit an electronic copy of your
request at many Federal Depository
Libraries.
B. When Will the Agency Grant a
Request for a Hearing?
A request for a hearing will be granted
if the Administrator determines that the
material submitted shows the following:
There is a genuine and substantial issue
of fact; there is a reasonable possibility
that available evidence identified by the
requestor would, if established resolve
one or more of such issues in favor of
the requestor, taking into account
uncontested claims or facts to the
contrary; and resolution of the factual
issues(s) in the manner sought by the
requestor would be adequate to justify
the action requested (40 CFR 178.32).
VI. Statutory and Executive Order
Reviews
This final rule establishes an
exemption from the tolerance
requirement 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 rule has been exempted
from review under Executive Order
12866 due to its lack of significance,
this rule is not subject to Executive
Order 13211, Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use (66
FR 28355, May 22, 2001). This final rule
does not contain any information
collections subject to OMB approval
under the Paperwork Reduction Act
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(PRA), 44 U.S.C. 3501 et seq., or impose
any enforceable duty or contain any
unfunded mandate as described under
Title II of the Unfunded Mandates
Reform Act of 1995 (UMRA) (Public
Law 104–4). 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); or OMB review or any Agency
action under Executive Order 13045,
entitled Protection of Children from
Environmental Health Risks and Safety
Risks (62 FR 19885, April 23, 1997).
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), Public Law 104–113, section
12(d) (15 U.S.C. 272 note). 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. In addition, the
Agency has determined that this action
will not have a substantial direct effect
on States, on the relationship between
the national government and the States,
or on the distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132, entitled
Federalism (64 FR 43255, August 10,
1999). Executive Order 13132 requires
EPA to develop an accountable process
to ensure ‘‘meaningful and timely input
by State and local officials in the
development of regulatory policies that
have federalism implications.’’ ‘‘Policies
that have federalism implications’’ is
defined in the Executive order to
include regulations that have
‘‘substantial direct effects on the States,
on the relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government.’’ This final rule
directly regulates growers, food
processors, food handlers and food
retailers, not States. This action does not
alter the relationships or distribution of
power and responsibilities established
by Congress in the preemption
provisions of FFDCA section 408(n)(4).
For these same reasons, the Agency has
determined that this rule does not have
any ‘‘tribal implications’’ as described
in Executive Order 13175, entitled
Consultation and Coordination with
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Indian Tribal Governments (65 FR
67249, November 6, 2000). Executive
Order 13175, requires EPA to develop
an accountable process to ensure
‘‘meaningful and timely input by tribal
officials in the development of
regulatory policies that have tribal
implications.’’ ‘‘Policies that have tribal
implications’’ is defined in the
Executive order to include regulations
that have ‘‘substantial direct effects on
one or more Indian tribes, on the
relationship between the Federal
Government and the Indian tribes, or on
the distribution of power and
responsibilities between the Federal
Government and Indian tribes.’’ This
rule will not have substantial direct
effects on tribal governments, on the
relationship between the Federal
Government and Indian tribes, or on the
distribution of power and
responsibilities between the Federal
Government and Indian tribes, as
specified in Executive Order 13175.
Thus, Executive Order 13175 does not
apply to this rule.
VII. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., as added by the Small
Business Regulatory Enforcement
Fairness Act of 1996, generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of the
Congress and to the Comptroller General
of the United States. 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 this final
rule in the Federal Register. This final
rule 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: April 14, 2005.
Lois Rossi,
Director, Registration Division, Office of
Pesticide Programs.
Therefore, 40 CFR Chapter I is
amended as follows:
I
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
I
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Section 180.460 paragraph (a) is
revised to read as follows:
I
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§ 180.460 Benoxacor; tolerances for
residues.
(a) General. Tolerances are
established for residues of the inert
ingredient (safener) benoxacor (4(dichloroacetyl)-3,4-dihydro-3-methyl2H-1, 4-benzoxazine) at 0.01 parts per
million (ppm) when used in pesticide
formulations containing metolachlor or
S-metolachlor in or on raw agricultural
commodities for which tolerances have
been established for metolachlor or Smetolachlor.
*
*
*
*
*
[FR Doc. 05–8119 Filed 4–26–05; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[OPP–2005–0046; FRL–7705–1]
Spiromesifen; Pesticide Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: This regulation establishes a
tolerance for: Primary crops for the
combined residues of spiromesifen (2oxo-3-(2,4,6-trimethylphenyl)-1oxaspiro[4.4]non-3-en-4-yl 3,3dimethylbutanoate) and its enol
metabolite (4-hydroxy-3-(2,4,6trimethylphenyl)-1-oxaspiro[4.4]non-3en-2-one), calculated as the parent
compound equivalents; rotational crops
for the inadvertent or indirect combined
residues of spiromesifen (2-oxo-3-(2,4,6trimethylphenyl)-1-oxaspiro[4.4]non-3en-4-yl 3,3-dimethylbutanoate), its enol
metabolite (4-hydroxy-3-(2,4,6trimethylphenyl)-1-oxaspiro[4.4]non-3en-2-one), and its metabolites
containing the 4-hydroxymethyl moiety
(4-hydroxy-3-[4-(hydroxymethyl)-2,6dimethylphenyl]-1-oxaspiro[4.4]non-3en-2-one), calculated as the parent
compound equivalents; and livestock
commodities for the combined residues
of spiromesifen (2-oxo-3-(2,4,6trimethylphenyl)-1-oxaspiro[4.4]non-3en-4-yl 3,3-dimethylbutanoate), and its
metabolites containing the enol (4hydroxy-3-(2,4,6-trimethylphenyl)-1oxaspiro[4.4]non-3-en-2-one) and 4hydroxymethyl (4-hydroxy-3-[4(hydroxymethyl)-2,6-dimethylphenyl]1-oxaspiro[4.4]non-3-en-2-one) moieties,
calculated as the parent compound
equivalents. Bayer CropScience
requested these tolerances under the
Federal Food, Drug, and Cosmetic Act
(FFDCA), as amended by the Food
Quality Protection Act of 1996 (FQPA).
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21631
This regulation is effective April
27, 2005. Objections and requests for
hearings must be received on or before
June 27, 2005.
ADDRESSES: To submit a written
objection or hearing request follow the
detailed instructions as provided in
Unit VI. of the SUPPLEMENTARY
INFORMATION. EPA has established a
docket for this action under Docket
identification (ID) number OPP–2005–
0046. All documents in the docket are
listed in the EDOCKET index at http:/
/www.epa.gov/edocket. Although listed
in the index, some information is not
publicly available, i.e., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the Internet and will be
publicly available only in hard copy
form. Publicly available docket
materials are available either
electronically in EDOCKET or in hard
copy at the Public Information and
Records Integrity Branch (PIRIB), Rm.
119, Crystal Mall #2, 1801 S. Bell St.,
Arlington, VA. This docket facility is
open from 8:30 a.m. to 4 p.m., Monday
through Friday, excluding legal
holidays. The docket telephone number
is (703) 305–5805.
FOR FURTHER INFORMATION CONTACT:
Thomas Harris, Registration Division
(7505C), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(703) 308–9423; e-mail address:
harris.thomas@epa.gov.
SUPPLEMENTARY INFORMATION:
DATES:
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. Potentially
affected entities may include, but are
not limited to:
• Crop production (NAICS 111), e.g.,
agricultural workers; greenhouse,
nursery, and floriculture workers;
farmers.
• Animal production (NAICS 112),
e.g., cattle ranchers and farmers, dairy
cattle farmers, livestock farmers.
• Food manufacturing (NAICS 311),
e.g., agricultural workers; farmers;
greenhouse, nursery, and floriculture
workers; ranchers; pesticide applicators.
• Pesticide manufacturing (NAICS
32532), e.g., agricultural workers;
commercial applicators; farmers;
greenhouse, nursery, and floriculture
workers; residential users.
This listing is not intended to be
exhaustive, but rather provides a guide
E:\FR\FM\27APR1.SGM
27APR1
Agencies
[Federal Register Volume 70, Number 80 (Wednesday, April 27, 2005)]
[Rules and Regulations]
[Pages 21628-21631]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-8119]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[OPP-2005-0080; FRL-7709-2]
Benoxacor; Partial Grant and Partial Denial of Petition, and
Amendment of Tolerance to Include S-Metolachlor
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: EPA is granting, in part, and denying, in part, pesticide
petition 7E3489 submitted by Syngenta Crop Protection, Inc., and is
amending the tolerance for benoxacor at 40 CFR 180.460 to include a
reference to S-metolachlor, in addition to the existing reference to
metolachlor. EPA issued a notice pursuant to section 408(d)(3) of
FFDCA, 21 U.S.C. 346a(d)(3) in the Federal Register of August 3, 2003
(68 FR 46620) (FRL-7317-6) announcing the filing of a petition
requesting that the tolerance expression for the inert ingredient
benoxacor (safener) in 40 CFR 180.460 be amended to remove references
to metolachlor and replace it with references to S-metoloachlor.
Although EPA finds it is safe to add a reference to S-metolachlor to
this tolerance regulation, EPA does not agree that grounds exist to
remove the reference to metolachlor. Thus, EPA is granting Syngenta's
petition in as far as it seeks to add the reference to S-metolachlor
but is denying the request to remove metolachlor.
DATES: This regulation is effective April 27, 2005. Objections and
requests for hearings must be received on or before June 27, 2005.
ADDRESSES: To submit a written objection or hearing request, follow the
detailed instructions as provided in Unit VIII. of the SUPPLEMENTARY
INFORMATION. EPA has established a docket for this action under Docket
identification (ID) number OPP-2005-0080. All documents in the docket
are listed in the EDOCKET index at https://www.epa.gov/edocket. Although
listed in the index, some information is not publicly available, i.e.,
CBI or other information whose disclosure is restricted by statute.
Certain other material, such as copyrighted material, is not placed on
the Internet and will be publicly available only in hard copy form.
Publicly available docket materials are available either electronically
in EDOCKET or in hard copy at the Public Information and Records
Integrity Branch (PIRIB), Rm. 119, Crystal Mall 2, 1801 S.
Bell St., Arlington, VA. This docket facility is open from 8:30 a.m. to
4 p.m., Monday through Friday, excluding legal holidays. The docket
telephone number is (703) 305-5805.
FOR FURTHER INFORMATION CONTACT: Karen Angulo, Registration Division
(7505C), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave, NW., Washington, DC 20460-0001; telephone
number: (703) 306-0404; e-mail address: angulo.karen@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.
Potentially affected entities may include, but are not limited to:
Crop production (NAICS code 111)
Animal production (NAICS code 112)
Food manufacturing (NAICS code 311)
Pesticide manufacturing (NAICS code 32532)
This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. Other types of entities not listed in this unit could also be
affected. The North American Industrial Classification System (NAICS)
codes have been provided to assist you and others in determining
whether this action might apply to certain entities. If you have any
questions regarding the applicability of this action to a particular
entity, consult the person listed under FOR FURTHER INFORMATION
CONTACT.
B. How Can I Access Electronic Copies of this Document and Other
Related Information?
In addition to using EDOCKET (https://www.epa.gov/edocket/), you may
access this Federal Register document electronically through the EPA
Internet under the ``Federal Register'' listings at https://www.epa.gov/
fedrgstr/. A frequently updated electronic version of 40 CFR part 180
is available at E-CFR Beta Site Two at https://www.gpoaccess.gov/ecfr/.
II. Background and Statutory Findings
In the Federal Register of August 6, 2003 (68 FR 46620) (FRL-7317-
6), EPA issued a notice pursuant to section 408(d)(3) of FFDCA, 21
U.S.C. 346a(d)(3), announcing the filing of pesticide petition (7E3489)
by Syngenta Crop Protection, Inc., P.O. Box 18300, Greensboro, NC
27419-8300. The petition requested that the tolerance expression for
the inert ingredient benoxacor (safener) in 40 CFR 180.460
[[Page 21629]]
be amended to remove the references to metolachlor and replace it with
references to S-metolachlor. Currently, the benoxacor tolerance permits
residues of benoxacor in or on raw agricultural commodities for which
tolerances have been established for the herbicide metolachlor when
benoxacor is used in pesticide formulations containing metolachlor.
Syngenta's petition seeks this amendment because it has voluntarily
canceled all its metolachlor product registrations, including its
metolachlor registrations containing the safener benoxacor, and has
registered products containing S-metolachlor in their place. Some or
all of these new registrations contain not only S-metolachlor but
benoxacor as well.
The notice of filing included a summary of Syngenta's petition. EPA
received one comment, which is discussed further in Unit IV.
This final rule is issued pursuant to section 408(d) of FFDCA, as
amended by the FQPA (21 U.S.C. 346a(d)). Section 408 of FFDCA
authorizes the establishment of tolerances, exemptions from the
requirement of a tolerance, modifications in tolerances, and revocation
of tolerances for residues of pesticide chemicals in or on raw
agricultural commodities and processed foods. Without a tolerance or
tolerance exemption, food containing pesticide residues is considered
to be unsafe and therefore ``adulterated'' under section 402(a) of the
FFDCA. If food containing pesticide residues is found to be
adulterated, the food may not be distributed in interstate commerce (21
U.S.C. 331(a) and 342 (a)).
III. What Action is the Agency Taking?
In this action, EPA is ruling on a petition (7E3489) filed by
Syngenta Crop Protection pursuant to FFDCA section 408(d) to amend a
tolerance regulation. Section 408(d)(4) authorizes EPA to act on a
petition by issuing a final rule adopting the amendment sought by the
petition, issuing a final rule that varies from the amendment sought by
the petition, or completely denying the petition. For the reasons
described below, EPA has chosen the middle course with regard to
Syngenta's petition - granting it only in part and denying the
remainder.
The Agency is granting Syngenta's petition in part. The Agency has
determined that the tolerance for benoxacor at 40 CFR 180.460 should be
amended to include a reference to both metolachlor and S-metolachlor.
EPA agrees there are sufficient grounds to amend the tolerance
expression for benoxacor to include a reference to S-metolachlor, the
product Syngenta is now marketing in place of the metolachlor
registrations it has voluntarily canceled. EPA has previously
determined that the existing benoxacor tolerances meet the safety
standard of FFDCA section 408(b)(2)(A)(i). See the Federal Register of
February 13, 1998, (63 FR 7299) (FRL-5771-1).
A chronic dietary exposure and risk assessment was conducted using
Dietary Exposure Evaluation Model-Food Commodity Intake Database (DEEM-
FCID\TM\), which uses food consumption data from the United States
Department of Agriculture's (USDA's) Continuing Surveys of Food Intakes
by Individuals (CSFII) from 1994-1996 and 1998. The chronic analysis
assumes tolerance-level residues on all crops with established,
pending, or proposed tolerances for metolachlor and/or S-metolachlor.
The analysis also assumes that 100% of the crops included in the
assessment were treated with metolachlor and/or S-metolachlor and its
safener, benoxacor. These assumptions result in over estimates of
exposure and are, therefore, highly conservative with respect to
dietary risk assessment. Even with these assumptions, the dietary risk
estimates for all population subgroups are less than 15% of the chronic
Population-Adjusted Dose (cPAD). Generally EPA is concerned when risk
estimates exceed 100% of the cPAD. Therefore, the dietary risk
estimates are below EPA's level of concern for all population
subgroups, including those of infants and children. There are no acute
toxicological or cancer concerns for benoxacor.
Accordingly, EPA finds for the reasons set forth in the Federal
Register notice of February 13, 1998 (63 FR 7299), establishing the
existing benoxacor tolerances, that these tolerances, as amended today,
are safe for the general population, including infants and children,
within the meaning of FFDCA section 408(b)(2)(A)(i).
EPA does not agree, however, that grounds exist to remove the
reference to metolachlor in 40 CFR 180.460 as requested by the
petition. As noted, EPA has found previously that residues of benoxacor
resulting from its use with metolachlor, are safe and will be safe
under the regulation when amended to also reference S-metolachlor.
Further, while Syngenta may have canceled its metolachlor
registrations, there are existing metolachlor registrations currently
held by other persons. The fact that one registrant of several has
chosen to stop marketing the pesticide does not constitute the
``abandonment'' of a pesticide as contemplated by 40 CFR 180.32(b) that
would justify the administrative amendment or repeal of a tolerance.
Further, as the commenter has made clear, existing metolachlor
registrants are interested in retaining the reference to metolachlor in
the benoxacor tolerance expression. For these reasons, EPA is denying
Syngenta's request to remove metolachlor from the existing tolerance
expression.
Based on its decision to grant, in part, and deny, in part,
Syngenta's petition, EPA is today amending the tolerance expression for
benoxacor at 40 CFR 180.460(a) as found in the regulatory section of
this document.
IV. Public Comments
As noted in Unit.II. of this document, EPA received a comment
objecting to Syngenta's petition to replace the references to
metolachlor in 40 CFR 180.460 with references to S-metolachlor.
Specifically, the commenter argues that the proposed amendment is
unnecessary to protect public health; that it would establish an
inappropriate precedent prior to the adoption of an isomer active
ingredient policy; and that the rationale for action that Syngenta has
offered is materially incomplete and inadequate. Because EPA has
decided for reasons set forth in Unit.III. of this document to retain
the references to metolachlor in 40 CFR 180.460, EPA need not reach the
commenter's arguments objecting to Syngenta's proposed deletion of
metolachlor from that regulation. The commenter also argues, however,
that as a general matter Syngenta's petition provides no pertinent new
``data, information and arguments'' or ``reasonable grounds'' in
support of the petition. EPA disagrees with this comment to the extent
it suggests there are inadequate grounds for adding references to S-
metolachlor to the tolerance expression at 40 CFR 180.460. As discussed
above, the petition noted that EPA has previously found that benoxacor
residues are safe and has determined that this action will not alter
the assumptions upon which that determination relied. Accordingly, EPA
believes reasonable grounds exist to add references to S-metolachlor to
40 CFR 180.460.
V. Objections and Hearing Requests
Under section 408(g) of the FFDCA, as amended by the FQPA, any
person may file an objection to any aspect of this regulation and may
also request a hearing on those objections. The EPA procedural
regulations which govern the submission of objections and requests
[[Page 21630]]
for hearings appear in 40 CFR part 178. Although the procedures in
those regulations require some modification to reflect the amendments
made to the FFDCA by the FQPA of 1996, EPA will continue to use those
procedures, with appropriate adjustments, until the necessary
modifications can be made. The new section 408(g) provides essentially
the same process for persons to ``object'' to a regulation for an
exemption from the requirement of a tolerance issued by EPA under new
section 408(d), as was provided in the old FFDCA sections 408 and 409.
However, the period for filing objections is now 60 days, rather than
30 days.
A. What Do I Need to Do to File an Objection or Request a Hearing?
You must file your objection or request a hearing on this
regulation in accordance with the instructions provided in this unit
and in 40 CFR part 178. To ensure proper receipt by EPA, you must
identify docket ID number OPP-2005-0080 in the subject line on the
first page of your submission. All requests must be in writing, and
must be mailed or delivered to the Hearing Clerk on or before June 27,
2005.
1. Filing the request. Your objection must specify the specific
provisions in the regulation that you object to, and the grounds for
the objections (40 CFR 178.25). If a hearing is requested, the
objections must include a statement of the factual issues(s) on which a
hearing is requested, the requestor's contentions on such issues, and a
summary of any evidence relied upon by the objector (40 CFR 178.27).
Information submitted in connection with an objection or hearing
request may be claimed confidential by marking any part or all of that
information as CBI. Information so marked will not be disclosed except
in accordance with procedures set forth in 40 CFR part 2. A copy of the
information that does not contain CBI must be submitted for inclusion
in the public record. Information not marked confidential may be
disclosed publicly by EPA without prior notice.
Mail your written request to: Office of the Hearing Clerk (1900L),
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001. You may also deliver your request to the
Office of the Hearing Clerk in Suite 350, 1099 14th St., NW.,
Washington, DC 20005. The Office of the Hearing Clerk is open from 8
a.m. to 4 p.m., Monday through Friday, excluding legal holidays. The
telephone number for the Office of the Hearing Clerk is (202) 564-6255.
2. Copies for the Docket. In addition to filing an objection or
hearing request with the Hearing Clerk as described in Unit VIII.A.,
you should also send a copy of your request to the PIRIB for its
inclusion in the official record that is described in ADDRESSES. Mail
your copies, identified by docket ID number OPP-2005-0080, to: Public
Information and Records Integrity Branch, Information Resources and
Services Division (7502C), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460.
In person or by courier, bring a copy to the location of the PIRIB
described in ADDRESSES. You may also send an electronic copy of your
request via e-mail to: opp-docket@epa.gov. Please use an ASCII file
format and avoid the use of special characters and any form of
encryption. Copies of electronic objections and hearing requests will
also be accepted on disks in WordPerfect 6.1/8.0 or ASCII file format.
Do not include any CBI in your electronic copy. You may also submit an
electronic copy of your request at many Federal Depository Libraries.
B. When Will the Agency Grant a Request for a Hearing?
A request for a hearing will be granted if the Administrator
determines that the material submitted shows the following: There is a
genuine and substantial issue of fact; there is a reasonable
possibility that available evidence identified by the requestor would,
if established resolve one or more of such issues in favor of the
requestor, taking into account uncontested claims or facts to the
contrary; and resolution of the factual issues(s) in the manner sought
by the requestor would be adequate to justify the action requested (40
CFR 178.32).
VI. Statutory and Executive Order Reviews
This final rule establishes an exemption from the tolerance
requirement 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 rule has been exempted from review under Executive
Order 12866 due to its lack of significance, this rule is not subject
to Executive Order 13211, Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use (66 FR 28355,
May 22, 2001). 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., or impose any enforceable duty or
contain any unfunded mandate as described under Title II of the
Unfunded Mandates Reform Act of 1995 (UMRA) (Public Law 104-4). 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);
or OMB review or any Agency action under Executive Order 13045,
entitled Protection of Children from Environmental Health Risks and
Safety Risks (62 FR 19885, April 23, 1997). 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),
Public Law 104-113, section 12(d) (15 U.S.C. 272 note). 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. In addition, the Agency has determined that this
action will not have a substantial direct effect on States, on the
relationship between the national government and the States, or on the
distribution of power and responsibilities among the various levels of
government, as specified in Executive Order 13132, entitled Federalism
(64 FR 43255, August 10, 1999). Executive Order 13132 requires EPA to
develop an accountable process to ensure ``meaningful and timely input
by State and local officials in the development of regulatory policies
that have federalism implications.'' ``Policies that have federalism
implications'' is defined in the Executive order to include regulations
that have ``substantial direct effects on the States, on the
relationship between the national government and the States, or on the
distribution of power and responsibilities among the various levels of
government.'' This final rule directly regulates growers, food
processors, food handlers and food retailers, not States. This action
does not alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). For these same reasons, the Agency has
determined that this rule does not have any ``tribal implications'' as
described in Executive Order 13175, entitled Consultation and
Coordination with
[[Page 21631]]
Indian Tribal Governments (65 FR 67249, November 6, 2000). Executive
Order 13175, requires EPA to develop an accountable process to ensure
``meaningful and timely input by tribal officials in the development of
regulatory policies that have tribal implications.'' ``Policies that
have tribal implications'' is defined in the Executive order to include
regulations that have ``substantial direct effects on one or more
Indian tribes, on the relationship between the Federal Government and
the Indian tribes, or on the distribution of power and responsibilities
between the Federal Government and Indian tribes.'' This rule will not
have substantial direct effects on tribal governments, on the
relationship between the Federal Government and Indian tribes, or on
the distribution of power and responsibilities between the Federal
Government and Indian tribes, as specified in Executive Order 13175.
Thus, Executive Order 13175 does not apply to this rule.
VII. Congressional Review Act
The Congressional Review Act, 5 U.S.C. 801 et seq., as added by the
Small Business Regulatory Enforcement Fairness Act of 1996, generally
provides that before a rule may take effect, the agency promulgating
the rule must submit a rule report, which includes a copy of the rule,
to each House of the Congress and to the Comptroller General of the
United States. 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 this final rule in the Federal Register. This final
rule 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: April 14, 2005.
Lois Rossi,
Director, Registration Division, Office of Pesticide Programs.
0
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. Section 180.460 paragraph (a) is revised to read as follows:
Sec. 180.460 Benoxacor; tolerances for residues.
(a) General. Tolerances are established for residues of the inert
ingredient (safener) benoxacor (4-(dichloroacetyl)-3,4-dihydro-3-
methyl-2H-1, 4-benzoxazine) at 0.01 parts per million (ppm) when used
in pesticide formulations containing metolachlor or S-metolachlor in or
on raw agricultural commodities for which tolerances have been
established for metolachlor or S-metolachlor.
* * * * *
[FR Doc. 05-8119 Filed 4-26-05; 8:45 am]
BILLING CODE 6560-50-S