Citrate Esters; Exemption from the Requirement of a Tolerance
[Federal Register: September 29, 2004 (Volume 69, Number 188)]
[Rules and Regulations]
[Page 58066-58071]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29se04-13]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[OPP-2004-0300; FRL-7677-6]
Citrate Esters; Exemption from the Requirement of a Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes exemptions from the requirement of
a tolerance for residues of acetyl tributyl citrate (ATBC) also known
as citric acid, 2-(acetyloxy)-, tributyl ester (CAS Reg. No. 77-90-7)
and triethyl citrate (TEC) also known as citric acid, triethyl ester
(CAS Reg. No. 77-93-0) when used as inert ingredients in pesticide
products. Morflex submitted a petition to EPA under the Federal Food,
Drug, and Cosmetic Act (FFDCA), as amended by the Food Quality
Protection Act of 1996 (FQPA), requesting the exemptions from the
requirement of a tolerance. This regulation eliminates the need to
establish a maximum permissible level for residues of ATBC or TEC.
DATES: This regulation is effective September 29, 2004. Objections and
requests for hearings must be received on or before November 29, 2004.
ADDRESSES: To submit a written objection or hearing request follow the
detailed instructions as provided in Unit XI. of the SUPPLEMENTARY
INFORMATION. EPA has established a docket for this action under Docket
identification (ID) number OPP-2004-0300. 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
[[Page 58067]]
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: Kathryn Boyle, Registration Division
(7505C), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone
number: (703) 305-6304; e-mail address: boyle.kathryn@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 Get Electronic Documents and Other Related Information?
In addition to using EDOCKET at (http://www.regulations.gov/), 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/.
II. Background and Statutory Findings
In the Federal Register of January 5, 2001 (66 FR 1129) (FRL-6761-
4), EPA issued a notice pursuant to section 408 of the FFDCA, 21 U.S.C.
346a, as amended by the FQPA (Public Law 104-170), announcing the
filing of pesticide petitions (PP (8E4966 and 8E4967) by Morflex Inc.,
2110 High Point Road, Greensboro, NC 27403. That notice included a
summary of the petition prepared by the petitioner.
The petition requested that 40 CFR 180.1001 (c), and (e) be amended
by establishing an exemption from the requirement of a tolerance for
residues of acetyl tributyl citrate (ATBC) also known as citric acid,
2-(acetyloxy)-, tributyl ester (CAS Reg. No. 77-90-7) and triethyl
citrate (TEC) also known as citric acid, triethyl ester (CAS Reg. No.
77-93-0). There were no comments received in response to the notice of
filing.
Section 408(b)(2)(A)(i) of the 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 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. 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. Inert Ingredient Definition
Inert ingredients are all ingredients that are not active
ingredients as defined in 40 CFR 153.125 and include, but are not
limited to, the following types of ingredients (except when they have a
pesticidal efficacy of their own): Solvents such as alcohols and
hydrocarbons; surfactants such as polyoxyethylene polymers and fatty
acids; carriers such as clay and diatomaceous earth; thickeners such as
carrageenan and modified cellulose; wetting, spreading, and dispersing
agents; propellants in aerosol dispensers; microencapsulating agents;
and emulsifiers. The term ``inert'' is not intended to imply
nontoxicity; the ingredient may or may not be chemically active.
Generally, EPA has exempted inert ingredients from the requirement of a
tolerance based on the low toxicity of the individual inert ingredients.
IV. Toxicological Profile
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 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. The nature of the toxic effects caused
by ATBC also known as citric acid, 2-(acetyloxy)-, tributyl ester (CAS
Reg. No. 77-90-7) and TEC also known as citric acid, triethyl ester
(CAS Reg. No. 77-93-0) are discussed in this unit. Both chemicals are
derivatives of citric acid. ATBC is prepared by esterification of butyl
alcohol with citric acid, followed by acetylation. TEC is prepared by
esterification of ethyl alcohol with citric acid.
The Agency evaluated the toxicity data base submitted by the
petitioner, Morflex which included a 2-generation reproductive study,
and several articles from open literature. Other reliable sources of
information used by the Agency in performing this assessment are
information from the internet on (1) World Health Organization (WHO)
evaluations, (2) British Industrial Biological Research Association
(BIBRA) abstracts, and (3) the Opinion of the European Commission,
Health and Consumer Protection Directorate-General (CSTEE), and (4)
structure-activity-relationship (SAR) assessments performed on
surrogate chemicals as prepared by the Agency's Office of Pollution
Prevention and Toxics. The toxicological databases for these chemicals
are a mixture of guideline studies performed in the last 15 years and
older studies from the 1970s and 1950s. These older studies are more
difficult to evaluate given the different standards of reporting that
existed some years ago.
Both ATBC and TEC have low acute oral toxicity (Toxicity Category
IV). Ocular irritation is moderate. Both are Toxicity Category IV for
dermal irritation. Neither are human sensitizers. Both chemicals have
been reviewed by other entities. None of these organizations indicated
any specific concerns for ATBC or TEC. Based on the submitted studies,
neither ATBC or TEC is mutagenic.
[[Page 58068]]
In a rat metabolism study, ATBC was readily absorbed and rapidly
excreted in urine and feces within 48 hours. The following metabolites
were detected in the urine: Acetyl citrate, monobutyl citrate, acetyl
monobutyl citrate, dibutyl citrate, and acetyl dibutyl citrate. ATBC
was hydrolyzed in both human and rat liver homogenates resulting in n-
butanol and tributyl citrate (TBC). However, in human serum the half-
life was 7 hours versus 30 minutes in the rat. These in vivo and in
vitro studies indicate that ATBC is hydrolysed.
No metabolism studies were reviewed for TEC. However, it is
expected that all citrate esters would undergo hydrolysis to citric
acid and the corresponding alcohol. For TEC, this would be ethanol. The
human body is able to effectively metabolize both ethanol and citric
acid. Thus, the human body has known pathways to metabolize TEC
hydrolysis metabolites.
The ATBC 2-generation reproductive toxicity study was recently re-
evaluated by the Agency. No adverse reproductive performance was
observed at any dose. The reproductive toxicity no observed adverse
level (NOAEL) was 1,000 milligrams/kilograms/day (mg/kg/day), the
highest dose tested. A lowest observed adverse level (LOAEL) was not
observed. The parental no observed level (NOEL) and the offspring NOEL
is 1,000 mg/kg/day. The parental lowest observed level (LOEL) and the
offspring LOEL was not observed.
The available information consists of the FDA-affirmed GRAS status
of TEC (21 CFR 184.1911), ATBC's approval as a synthetic flavoring
substance under 21 CFR 172.515, the approval of both ATBC and TEC under
21 CFR 181.27 as prior sanctioned plasticizers, the abstracts of the
BIBRA toxicity profiles, several evaluations by the World Health
Organization, the SAR assessments of the structurally-related
chemicals, the CSTEE Opinion, and the toxicity studies submitted by the
petitioner. Taken together the weight of evidence of the available
information indicate chemicals of lower toxicity.
Greater detail on the Agency's review and evaluation of the
submitted studies and articles from open literature are in the ATBC and
TEC Science Assessment in EDOCKET at (http://www.regulations.gov/) (See
OPP-2004-0300).
V. Aggregate Exposures
In examining aggregate exposure, section 408 of the FFDCA 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).
EPA establishes exemptions from the requirement of a tolerance only
in those cases where it can be clearly demonstrated that the risks from
aggregate exposure to pesticide chemical residues under reasonably
foreseeable circumstances will pose no appreciable risks to human
health. In order to determine the risks from aggregate exposure to
pesticide inert ingredients, the Agency considers the toxicity of the
inert in conjunction with possible exposure to residues of the inert
ingredient through food, drinking water, and through other exposures
that occur as a result of pesticide use in residential settings. If EPA
is able to determine that a finite tolerance is not necessary to ensure
that there is a reasonable certainty that no harm will result from
aggregate exposure to the inert ingredient, an exemption from the
requirement of a tolerance may be established.
Various publicly-available screening-level models were used to
estimate some of the existing levels of exposure that could occur in
and around the home. To assure protectiveness, these models create
estimates that are deliberately intended to over-estimate exposure. All
modeling (with the exception of the CSTEE plastic toy scenario) was
performed by EPA. The highest potential exposure level was 0.422 mg/kg/
day for children (1-2 years old) for dietary exposure through
consumption of food (as a result of application of a pesticide product
containing either ATBC or TEC to crops). All of the screening-level
exposures are much less than any of the NOAELs/NOELs from the repeated
dose oral toxicity studies. Greater detail on the Agency's exposure
assessment are in the ATBC and TEC Science Assessment in EDOCKET at
(http://www.regulations.gov/) (See OPP-2004-0300).
VI. Cumulative Effects
Section 408(b)(2)(D)(v) of the FFDCA requires that, when
considering whether to establish, modify, or revoke a tolerance, the
Agency consider ``available information'' concerning the cumulative
effects of a particular pesticide's residues and ``other substances
that have a common mechanism of toxicity.''
Unlike other pesticides for which EPA has followed a cumulative
risk approach based on a common mechanism of toxicity, EPA has not made
a common mechanism of toxicity finding as to acetyl tributyl citrate,
triethyl citrate or any citrate esters. These esters do not appear to
produce a toxic metabolite produced by other substances. These are
lower toxicity chemicals; therefore, the resultant risks separately
and/or combined should also be low. For the purposes of this action,
therefore, EPA has not assumed that acetyl tributyl citrate or triethyl
citrate 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 the policy statements released by EPA's Office of
Pesticide Programs concerning common mechanism determinations and
procedures for cumulating effects from substances found to have a
common mechanism on EPA's website at
http://www.epa.gov/pesticides/cumulative/.
VII. Children's Safety Factor
The toxicity database for ATBC includes a rat oral reproductive
toxicity study in which NOELs of 1,000 mg/kg/day were identified. There
are also the SARs on structurally-related citrate esters which did not
indicate any concerns for developmental or reproductive toxicity.
ATBC, given the additional acetylation step, is the more complex,
larger molecule. The acetylation step also increases the number of
possible metabolites as evidenced by the results of the ATBC rat
metabolism study. ATBC data can be used as surrogate data for TEC. TEC
cannot be used as surrogate data for ATBC. ATBC is the more toxic of
the two chemicals and has the larger available data base.
There is sufficient information for the Agency to judge the
potential for developmental and reproductive effects of ATBC and TEC.
No additional data are needed to assess the toxicity of ATBC and TEC.
There is no reason to expect that the reasonably, foreseeable uses of
ATBC and TEC will constitute any significant hazard. EPA has not used a
safety factor analysis to assess the risk. For the same reasons the
additional tenfold safety factor is unnecessary.
VIII. Determination of Safety for U.S. Population, Infants and Children
The Agency believes that ATBC and TEC are of low toxicity. Of
highest consideration in this judgement is the body's ability to
effectively metabolize both ATBC and TEC to citric acid and the
corresponding alcohols. The metabolism studies provided by the
petitioner were helpful in reaching this determination. Both of these
chemicals
[[Page 58069]]
are well-studied. FDA, WHO, and CSTEE have all conducted assessments on
the uses of these chemicals. No toxicological concerns were specified
in any of the reviews and evaluations.
The Agency has used various screening-level models to estimate some
of the existing levels of exposure to ATBC and TEC. To assure
protectiveness, these estimates are deliberately intended to over-
estimate exposure. Given the consistent pattern of NOAELs/NOELs of
1,000 mg/kg/day, an understanding of the metabolism of ATBC and TEC,
and a significant gap between very over-estimated exposure numbers and
the NOAELs/NOELs, there is no need to pursue further numerical
refinements to the estimated exposures.
EPA concludes that there is a reasonable certainty of no harm from
aggregate exposure to residues of citric acid, 2-(acetyloxy)-, tributyl
ester (CAS Reg. No. 77-90-7) and citric acid, triethyl ester (CAS Reg.
No. 77-93-0). Accordingly, EPA finds that exempting citric acid, 2-
(acetyloxy)-, tributyl ester (CAS Reg. No. 77-90-7) and citric acid,
triethyl ester (CAS Reg. No. 77-93-0) will be safe.
IX. Other Considerations
A. Endocrine Disruptors
FQPA requires EPA to develop a screening program to determine
whether certain substances, including all pesticide chemicals (both
inert and active ingredients), ``may have an effect in humans that is
similar to an effect produced by a naturally occurring estrogen, or
such other endocrine effect.'' EPA has been working with interested
stakeholders to develop a screening and testing program as well as a
priority setting scheme. As the Agency proceeds with implementation of
this program, further testing of products containing ATBC and TEC for
endocrine effects may be required.
B. Analytical Method
An analytical method is not required for enforcement purposes since
the Agency is establishing an exemption from the requirement of a
tolerance without any numerical limitation.
C. Existing Exemptions
There is an existing tolerance exemption for acetyl tributyl
citrate (CAS Reg. No. 77-90-7) in 40 CFR 180.930 when used as a
component of plastic animal tags.
D. International Tolerances
The Agency is not aware of any country requiring a tolerance for
ATBC or TEC nor have any CODEX maximum residue levels been established
for any food crops at this time.
E. List 4A (Minimal Risk) Classification
The Agency established 40 CFR 180.950 (see the rationale in the
proposed rule published January 15, 2002 (67 FR 1925) (FRL-6807-8)) to
collect the tolerance exemptions for those substances classified as
List 4A, i.e., minimal risk substances. As part of evaluating an inert
ingredient and establishing the tolerance exemption, the Agency
determines the chemical's list classification. Given the available
information which indicates the body's ability to effectively
metabolize both ATBC and TEC to citric acid and the corresponding
alcohols and the consistent pattern of NOAELs/NOELs of 1,000 mg/kg/day,
citric acid, 2-(acetyloxy)-, tributyl ester (CAS Reg. No. 77-90-7) and
citric acid, triethyl ester (CAS Reg. No. 77-93-0) are to be classified
as List 4A inert ingredients.
X. Conclusions
Based on the information in this preamble, EPA concludes that there
is a reasonable certainty of no harm from aggregate exposure to
residues of acetyl tributyl citrate (ATBC) also known as citric acid,
2-(acetyloxy)-, tributyl ester (CAS Reg. No. 77-90-7) and triethyl
citrate (TEC) also known as citric acid, triethyl ester (CAS Reg. No.
77-93-0) Accordingly, EPA finds that exempting citric acid, 2-
(acetyloxy)-, tributyl ester (CAS Reg. No. 77-90-7) and citric acid,
triethyl ester (CAS Reg. No. 77-93-0) from the requirement of a
tolerance will be safe.
Therefore, the exemptions from the requirement of a tolerance for
citric acid, 2-(acetyloxy)-, tributyl ester (CAS Reg. No. 77-90-7) and
citric acid, triethyl ester (CAS Reg. No. 77-93-0) are established in
40 CFR 180.950. Since the tolerance exemptions are established under 40
CFR 180.950, the existing tolerance exemption for acetyl tributyl
citrate (CAS Reg. No. 77-90-7) in 40 CFR 180.930 is a duplication, and
will be removed.
XI. 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 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)
of the FFDCA, as was provided in the old FFDCA 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-2004-0300 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 November
29, 2004.
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 14\th\ 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 XI.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
[[Page 58070]]
copies, identified by docket ID number OPP-2004-0300, 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: 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).
XII. Statutory and Executive Order Reviews
This final rule establishes two exemptions from the tolerance
requirement 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 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. 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 (59 FR 22951,
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.
XIII. 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: September 14, 2004.
Lois Rossi,
Director, Registration Division, 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. In Sec. 180.930, the table is amended by removing the entry for
``acetyl tributyl citrate'' (CAS Reg. No. 77-90-7).
3. In Sec. 180.950, the table in paragraph (e) is amended by
adding alphabetically
[[Page 58071]]
the following inert ingredients to read as follows
Sec. 180.950 Tolerance exemptions for minimal risk active and inert
ingredients.
* * * * *
(e) * * *
------------------------------------------------------------------------
Chemical Name CAS No.
------------------------------------------------------------------------
* * * * *
Citric acid, 2-(acetyloxy)-, tributyl ester.......... 77-90-7
* * * * *
Citric acid, triethyl ester.......................... 77-93-0
* * * * *
------------------------------------------------------------------------
[FR Doc. 04-21587 Filed 9-28-04; 8:45 am]
BILLING CODE 6560-50-S