[Federal Register Volume 70, Number 125 (Thursday, June 30, 2005)]
[Rules and Regulations]
[Pages 37683-37688]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 05-12921]


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ENVIRONMENTAL PROTECTION AGENCY

40 CFR Part 180

[OPP-2005-0119; FRL-7718-3]


Cyprodinil; Time-Limited Pesticide Tolerance

AGENCY: Environmental Protection Agency (EPA).

ACTION: Final rule.

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[[Page 37684]]

SUMMARY: This regulation re-establishes time-limited tolerances for 
residues of cyprodinil, 4-cyclopropyl-6-methyl-N-phenyl-2-
pyrimidinamine in or on onion, dry bulb; onion, green; and strawberry. 
Interregional Research Project Number 4 (IR-4) requested these 
tolerances under the Federal Food, Drug, and Cosmetic Act (FFDCA), as 
amended by the Food Quality Protection Act of 1996 (FQPA). These 
tolerances will expire on December 31, 2007.

DATES: This regulation is effective June 30, 2005. Objections and 
requests for hearings must be received on or before August 29, 2005.

ADDRESSES: To submit a written objection or hearing request follow the 
detailed instructions as provided in Unit VII. of the SUPPLEMENTARY 
INFORMATION. EPA has established a docket for this action under Docket 
identification (ID) number OPP-2005-0119. 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: Barbara Madden, Registration Division 
(7505C), Office of Pesticide Programs, Environmental Protection Agency, 
1200 Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone 
number: (703) 305-6463; e-mail address: [email protected].

SUPPLEMENTARY INFORMATION:

I. General Information

A. Does this Action Apply to Me?

    You may be potentially affected by this action if you are an 
agricultural producer, food manufacturer, or pesticide manufacturer. 
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 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. To determine 
whether you or your business may be affected by this action, you should 
carefully examine the applicability provisions discussed above. 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 http://www.epa.gov/fedrgstr/. A frequently updated electronic version of 40 CFR part 180 
is available at E-CFR Beta Site Two at http://www.gpoaccess.gov/ecfr/. 
To access the OPPTS Harmonized Guidelines referenced in this document, 
go directly to the guidelines at http://www.epa.gpo/opptsfrs/home/guidelin.htm/.

II. Background and Statutory Findings

    In the Federal Register of January 7, 2005 (70 FR 1435) (FRL-7694-
3), EPA issued a notice pursuant to section 408(d)(3) of the FFDCA, 21 
U.S.C. 346a(d)(3), announcing the filing of a pesticide petition (PP 
8E5012) by IR-4, 681 US Highway 1 South, North Brunswick, NJ 
08902-3390. The petition requested that 40 CFR 180.532 be amended by 
extending the time-limited tolerances to December 31, 2007, for 
residues of the fungicide, cyprodinil, 4-cyclopropyl-6- methyl-N-
phenyl-2-pyrimidinamine in or on the raw agricultural commodities 
onion, dry bulb at 0.60 part per million (ppm); onion, green at 4.0 
ppm; and strawberry at 5.0 ppm. This notice included a summary of the 
petition prepared by Syngenta Crop Protection, Inc., the registrant. 
Comments were received from one individual opposing and objecting to 
the establishment of tolerances for residues of cyprodinil. The 
individual criticized IR-4's involvement in the pesticide registration 
as well as EPA's way of conducting pesticide registration. EPA's 
response to the public comments received is in Unit V. of this 
document. The tolerances will expire on December 31, 2007.
    Section 408(b)(2)(A)(i) of the FFDCA allows EPA to establish a 
tolerance (the legal limit for a pesticide chemical residue in or on a 
food) only if EPA determines that the tolerance is ``safe.'' Section 
408(b)(2)(A)(ii) of the FFDCA defines ``safe'' to mean that ``there is 
a reasonable certainty that no harm will result from aggregate exposure 
to the pesticide chemical residue, including all anticipated dietary 
exposures and all other exposures for which there is reliable 
information.'' This includes exposure through drinking water and in 
residential settings, but does not include occupational exposure. 
Section 408(b)(2)(C) of the FFDCA requires EPA to give special 
consideration to exposure of infants and children to the pesticide 
chemical residue in establishing a tolerance and to ``ensure that there 
is a reasonable certainty that no harm will result to infants and 
children from aggregate exposure to the pesticide chemical residue. . . 
.''
    EPA performs a number of analyses to determine the risks from 
aggregate exposure to pesticide residues. For further discussion of the 
regulatory requirements of section 408 of the FFDCA and a complete 
description of the risk assessment process, see the final rule on 
Bifenthrin Pesticide Tolerances (62 FR 62961, November 26, 1997) (FRL-
5754-7).

III. Aggregate Risk Assessment and Determination of Safety

    Consistent with section 408(b)(2)(D) of the FFDCA, EPA has reviewed 
the available scientific data and other relevant information in support 
of this action. EPA has sufficient data to assess the hazards of and to 
make a determination on aggregate exposure, consistent with section 
408(b)(2) of the FFDCA, for tolerances for residues of cyprodinil on 
onion, dry bulb at 0.60 ppm; onion, green at 4.0 ppm; and strawberry at 
5.0 ppm.
    In the Federal Register of September 23, 2003 (68 FR 54808, FRL-
7326-4) the Agency published a Final rule establishing tolerances for 
residues of cyprodinil in or on brassica, head and stem, subgroup 5A; 
brassica, leafy

[[Page 37685]]

greens, subgroup 5B; carrot; herb, subgroup 19A, dried; herb, subgroup 
19A, fresh; longan; lychee; pulasan; rambutan; Spanish lime; and 
turnip, greens. When the Agency conducted the risk assessments in 
support of this tolerance action it assumed that cyprodinil residues 
would be present on dry bulb onion, green onion and strawberry as well 
as on all foods covered by the proposed and established tolerances. 
Residues on dry bulb onion, green onion and strawberry were included 
because there were existing time-limited tolerances for these 
commodities. Therefore, re-establishing the dry bulb onion, green onion 
and strawberry tolerances will not change the most recent estimated 
aggregate risks resulting from use of cyprodinil, as discussed in the 
September 19, 2003 Federal Register (68 FR 54808, FRL-7326-4). Refer to 
the September 19, 2003 Federal Register document for a detailed 
discussion of the aggregate risk assessments and determination of 
safety. EPA relies upon those risk assessments and the findings made in 
the Federal Register document in support of this action. Below is a 
brief summary of the estimated aggregate risks from potential exposures 
to cyprodinil.
    Acute dietary risk assessments are performed for a food-use 
pesticide, if a toxicological study has indicated the possibility of an 
effect of concern occurring as a result of a one-day or single 
exposure. An acute Population Adjusted Dose (aPAD) of 1.5 mg/kg/day has 
been identified for females 13-49 years.
    In conducting the acute dietary risk assessment EPA used the 
Dietary Exposure Evaluation Model software with the Food Commodity 
Intake Database (DEEM-FCID\TM\), which incorporates food consumption 
data as reported by respondents in the USDA 1994-1996 and 1998 
Nationwide Continuing Surveys of Food Intake by Individuals (CSFII), 
and accumulated exposure to the chemical for each commodity. The 
following assumptions were made for the acute exposure assessments: An 
unrefined, Tier 1 acute dietary exposure assessment (using tolerance-
level residues, DEEM\TM\ (version 7.76) default processing factors and 
assuming 100% crop treated for all proposed commodities) was conducted 
for the females 13-49 years old population subgroup.
    The acute dietary exposure from food to cyprodinil will occupy 2% 
of the aPAD for the females 13-49 years old. In addition, there is 
potential for acute dietary exposure to cyprodinil in drinking water. 
After calculating drinking water levels of comparison (DWLOCs) and 
comparing them to the estimated environmental concentrations (EECs) for 
surface water and ground water, EPA does not expect the aggregate 
exposure to exceed 100% of the aPAD, as shown in Table 1 of this unit:

                      Table 1.--Aggregate Risk Assessment for Acute Exposure to Cyprodinil
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                                                                             Surface       Ground
              Population Subgroup/                aPAD (mg/     % aPAD/     Water EEC/   Water EEC/  Acute DWLOC/
                                                     kg)         (Food)       (ppb)        (ppb)        (ppb)
----------------------------------------------------------------------------------------------------------------
Females 13-49 years old                                  1.5            2         32.9         0.16       44,000
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    A chronic Population Adjusted Dose (cPAD) of 0.03 mg/kg/day has 
been identified for all population subgroups. In conducting the chronic 
dietary risk assessment EPA used DEEM-FCID\TM\, which incorporates food 
consumption data as reported by respondents in the USDA 1994-1996 and 
1998 Nationwide Continuing Surveys of Food Intake by Individuals 
(CSFII), and accumulated exposure to the chemical for each commodity. 
The following assumptions were made for the chronic exposure 
assessment: An unrefined, Tier 1 chronic dietary exposure assessment 
(using tolerance-level residues, DEEM default processing factors, and 
assuming 100% crop treated for all proposed commodities) was conducted 
for the general U.S. population and various population subgroups.
    EPA has concluded that exposure to cyprodinil from food will 
utilize 25% of the cPAD for the U.S. population, 65% of the cPAD for 
(the most highly exposed population subgroup) children 1-2 years old, 
32% of the cPAD for all infants <1 year old, and 21% of the cPAD for 
females 13-49 years old. Cyprodinil is not registered for use on any 
sites that would result in residential exposure. In addition, there is 
potential for chronic dietary exposure to cyprodinil in drinking water. 
After calculating DWLOCs and comparing them to the EECs for surface and 
ground water, EPA does not expect the aggregate exposure to exceed 100% 
of the cPAD, as shown in the following Table 2:

               Table 2. Aggregate Risk Assessment for Chronic (Non-Cancer) Exposure to Cyprodinil
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                                                                             Surface      Ground/
              Population/Subgroup                cPAD/mg/kg/    %/cPAD/     Water EEC/   Water EEC/    Chronic/
                                                     day         (Food)       (ppb)        (ppb)     DWLOC (ppb)
----------------------------------------------------------------------------------------------------------------
U.S. Population                                         0.03           25          8.1         0.16          790
 
sAll infants < 1 year old                               0.03           32          8.1         0.16          200
 
sChildren 1 - 2 years old                               0.03           65          8.1         0.16          100
 
sFemales 13 - 49 years old                              0.03           21          8.1         0.16          710
----------------------------------------------------------------------------------------------------------------


[[Page 37686]]

    Based on these risk assessments, EPA concludes that there is a 
reasonable certainty that no harm will result to the general 
population, and to infants and children from aggregate exposure to 
cyprodinil residues.

IV. Other Considerations

A. Analytical Enforcement Methodology

    The results of Multiresidue Method testing of cyprodinil and its 
metabolite CGA-232449 have been forwarded to the Food and Drug 
Administration (FDA). Cyprodinil was tested according to the FDA 
Multiresidue protocols (Protocols C, D, and E), and acceptable 
recoveries were obtained for cyprodinil fortified in apples at 0.50 ppm 
using Protocol D. The petitioner is proposing the Method AG-631A as a 
tolerance enforcement method for residues of cyprodinil in/on the 
subject crops. The method includes confirmatory procedures using gas 
chromatography/nitrogen/phosphorus detector (GC/NPD). The method has 
successfully undergone radiovalidation using 14C-labeled tomato samples 
and independent laboraory validation. In addition, the method has been 
the subject of acceptable Agency petition method validations on stone 
fruits and almond nutmeat and hulls. The method may be requested from: 
Chief, Analytical Chemistry Branch, Environmental Science Center, 701 
Mapes Rd., Ft. Meade, MD 20755-5350; telephone number: (410) 305-2905; 
e-mail address: [email protected].

B. International Residue Limits

    Canada, Codex, and Mexico do not have maximum residue limits (MRLs) 
for residues of cyprodinil in/on the proposed crops. Therefore, 
harmonization is not an issue.

V. EPA's Response to Public Comments Received Regarding the Notice of 
Filing

    Comments were received from one individual opposing and objecting 
to the extension of tolerances for residues of cyprodinil. The 
individual criticized IR-4's involvement in the pesticide registration 
as well as EPA's way of conducting pesticide registration. The comments 
were in response to the notice of filing published in the Federal 
Register of January 7, 2005 (70 FR 1435) (FRL-7694-3). The 
communication objected to extension of the proposed tolerances for 
several reasons and mostly involved generalized and unsubstantiated 
disagreement with EPA's risk assessment methodologies or safety 
findings. Each comment is listed below, followed by the Agency 
response.
    One comment indicated that IR-4 and Rutgers University are pushing 
more toxics upon this nation. Agency response: Although the concerns 
regarding IR-4 and Rutgers University to seek pesticide tolerances and 
registrations are not germane to EPA's statutory basis for acting on 
the cyprodinil tolerance petition, and thus technically no response is 
required to this comment, EPA can provide the following information 
regarding the Interregional Research Project Number 4 (IR-4). The IR-4 
program was created by Congress in 1963 in order to assist minor crop 
growers in the process of obtaining pesticide registrations. IR-4 
National Coordinating Headquarters is located at Rutgers University in 
New Jersey and receives the majority (90%) of its funding from the 
USDA. It is the only publicly funded program that conducts research and 
submits petitions for tolerances. IR-4 operates in collaboration with 
USDA, the Land Grant University System, the agrochemical industry, 
commodity associations, and EPA. IR-4 identifies needs, prioritizes 
accordingly, and conducts research. The majority (over 80%) of IR-4's 
research is conducted on reduced-risk chemicals. In addition to the 
work done in pesticide registration, IR-4 develops risk mitigation 
measures for existing registered products.
    Another comment noted that 8.4% of the chronic reference dose (RfD) 
for children 1 to 2 year old is contemplated and that this was done for 
profiteering and will harm children. Agency Response: For dietary risk 
assessment (other than cancer) a chronic RfD represents the dose at 
which no adverse effects are observed (the NOAEL) from the toxicology 
study identified as appropriate for use in risk assessment with an 
uncertainty factor (UF) applied to reflect uncertainties inherent in 
the extrapolation from laboratory animal data to humans and in the 
variations in sensitivity among members of the human population as well 
as other unknowns. For cyprodinil an UF of 100 was used, 10X to account 
for interspecies differences and 10X for intraspecies differences (RfD 
= NOAEL/UF). Given the use of a NOAEL and UF to calculate the chronic 
RfD the Agency feels that estimated exposures less than 100% of the 
chronic RfD will be protective of the general population, and to 
infants and children.
    An additional comment indicated that the standard for a 
``reasonable certainty'' is simply not a high enough standard. Agency 
Response: Under the existing legal framework provided by section 408 of 
the FFDCA, EPA is authorized to establish pesticide tolerances or 
exemptions where persons seeking such tolerances or exemptions have 
demonstrated that the pesticide meets the safety standard imposed by 
that statute. Section 408(b)(2)(A)(i) of the FFDCA allows EPA to 
establish a tolerance (the legal limit for a pesticide chemical residue 
in or on a food) only if EPA determines that the tolerance is ``safe.'' 
Section 408(b)(2)(A)(ii) of the 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.''
    A final comment stated that this chemical should not be allowed to 
be sold until the Agency has determined if cyprodinil has a common 
mechanism of toxicity with other pesticides. Agency response: The 
comment applied to the use of ``available data'' concerning the 
cumulative effects of the pesticide's residues and ''other substances 
that have a common mechanism of toxicity.`` In this case, EPA did not 
assume that this chemical has a common mechanism of toxicity with other 
substances as the chemical does not generate metabolites produced also 
by other chemicals. For specific information regarding EPA's approach 
to the use of common mechanism of toxicity to evaluate the cumulative 
effects of chemicals, please refer to EPA's website at http://www.epa.gov/pesticides/cumulative/ to see policy statements.
    In conclusion, the comments contained no scientific data or other 
substantive evidence to rebut the Agency's conclusion that there is a 
reasonable certainty that no harm will result from aggregate exposure 
to cyprodinil from the re-establishment of these tolerances.

VI. Conclusion

    Therefore, these tolerances are re-established for residues of 
cyprodinil, 4-cyclopropyl-6-methyl-N-phenyl-2-pyrimidinamine, in or on 
onion, dry bulb at 0.60 ppm, onion, green at 4.0 ppm, and strawberry at 
5.0 ppm.

VII. 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 for 
hearings appear in 40 CFR part 178. Although the procedures in those 
regulations require some modification to reflect the amendments made to 
the

[[Page 37687]]

FFDCA by the FQPA, EPA will continue to use those procedures, with 
appropriate adjustments, until the necessary modifications can be made. 
The new section 408(g) of the FFDCA 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 sections 408 and 409 of the FFDCA. 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-2005-0119 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 August 
29, 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 VI.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-2005-0119, 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-
0001. 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: [email protected]. 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).

VIII. Statutory and Executive Order Reviews

    This final rule establishes a tolerance under section 408(d) of the 
FFDCA 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 section 408(d) of the FFDCA, 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 section 408(n)(4) of the FFDCA. 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 Indian Tribal Governments (65 FR 
67249, November 6, 2000). Executive Order 13175, requires EPA to 
develop an accountable process to ensure

[[Page 37688]]

``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.

IX. 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: June 21, 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.


Sec.  180.532  [Amended]

0
2. In Sec.  180.532, in the table to paragraph (a)(2), amend the 
entries for ``Onion, dry bulb''; ``Onion, green''; and ``Strawberry'' 
by revising the expiration date ``12/31/04'' to read ``12/31/07.''

[FR Doc. 05-12921 Filed 6-29-05; 8:45 am]
BILLING CODE 6560-50-S