Polyvinyl Chloride; Tolerance Exemption
Note: EPA no longer updates this information, but it may be useful as a reference or resource.
[Federal Register: June 10, 1998 (Volume 63, Number 111)]
[Rules and Regulations]
[Page 31642-31645]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr10jn98-28]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[OPP-300656; FRL-5789-7]
RIN 2070-AB78
Polyvinyl Chloride; Tolerance Exemption
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes an exemption from the requirement
of a tolerance for residues of polyvinyl chloride when used as an inert
ingredient carrier in pesticide formulations applied to growing crops
or raw agricultural commodities after harvest. American Cyanamid
Company requested this exemption from the requirement of a tolerance
under the Federal Food, Drug and Cosmetic Act (FFDCA), as amended by
the Food Quality Protection Act of 1996 (Pub. L. 104-170).
DATES: This regulation is effective June 10, 1998. Objections and
requests for hearings must be received by EPA on or before August 10,
1998.
ADDRESSES: Written objections and hearing requests, identified by the
docket control number, OPP-300656, must be submitted to: Hearing Clerk
(1900), Environmental Protection Agency, Rm. M3708, 401 M St., SW.,
Washington, DC 20460. Fees accompanying objections and hearing requests
shall be labeled ``Tolerance Petition Fees'' and forwarded to: EPA
Headquarters Accounting Operations Branch, OPP (Tolerance Fees), P.O.
Box 360277M, Pittsburgh, PA 15251. A copy of any objections and hearing
requests filed with the Hearing Clerk identified by the docket control
number, OPP-300656, must also be submitted to: Public Information and
Records Integrity Branch, Information Resources and Services Division
(7502C), Office of Pesticide Programs, Environmental Protection Agency,
401 M St., SW., Washington, DC 20460. In person, bring a copy of
objections and hearing requests to Rm. 119, CM #2, 1921 Jefferson Davis
Hwy., Arlington, VA.
A copy of objections and hearing requests filed with the Hearing
Clerk may also be submitted electronically by sending electronic mail
(e-mail) to: opp-docket@epamail.epa.gov. Copies of objections and
hearing requests must be submitted as an ASCII file avoiding the use of
special characters and any form of encryption. Copies of objections and
hearing requests will also be accepted on disks in WordPerfect 5.1/6.1
file format or ASCII file format. All copies of objections and hearing
requests in electronic form must be identified by the docket control
number OPP-300656. No Confidential Business Information (CBI) should be
submitted through e-mail. Electronic copies of objections and hearing
requests on this rule may be filed online at many Federal Depository
Libraries.
FOR FURTHER INFORMATION CONTACT: By mail: Bipin Gandhi, Registration
Division 7505W, Office of Pesticide Programs, Environmental Protection
Agency, 401 M St., SW., Washington, DC 20460. Office location,
telephone number, and e-mail address: Fourth Floor, CS#1, 2800 Crystal
Drive, Arlington, VA, (703) 308-8380, e-mail:
gandhi.bipin@epamail.epa.gov.
SUPPLEMENTARY INFORMATION: In the Federal Register of August 29, 1997
(62 FR 45804) (FRL-5738-2), EPA issued a notice pursuant to section 408
of the Federal Food, Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 346a(e)
announcing the filing of pesticide petition (PP) 3E4246 for a tolerance
exemption by American Cyanamid Company, Agricultural Products Research
Division, P.O. Box 400, Princeton, NJ 08543-0400. This notice included
a summary of the petition prepared by American Cyanamid Company, the
petitioner. There were no comments received in response to the notice
of filing.
The petition requested that 40 CFR 180.1001 be amended by
establishing an exemption from the requirement of a tolerance for
residues of polyvinyl chloride when used as an inert ingredient carrier
in pesticide formulations applied to growing crops or raw agricultural
commodities after harvest.
I. Background and Statutory Authority
The Food Quality Protection Act of 1996 (FQPA) (Pub. L. 104-170)
was signed into law August 3, 1996. FQPA amends both the Federal Food,
Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 301 et seq., and the Federal
Insecticide, Fungicide, and Rodenticide Act (FIFRA), 7 U.S.C. 136 et
seq. The FQPA amendments went into effect immediately. Among other
things, FQPA amends FFDCA to bring all EPA pesticide tolerance-setting
activities
[[Page 31643]]
under a new section 408 with a new safety standard and new procedures.
New section 408(c)(2)(A)(i) allows EPA to establish an exemption
from the requirement of a tolerance for a pesticide chemical residue on
food only if EPA determines that the exemption is ``safe.'' Section
408(c)(2)(A)(ii) 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, but does not include
occupational exposure. Section 408(c)(2)(B) requires EPA to give
special consideration to exposure of infants and children to the
pesticide chemical residue in establishing an exemption from the
requirement of 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'' and specifies
factors EPA is to consider in establishing an exemption.
II. 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; surfactant 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.
III. Risk Assessment and Statutory Findings
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 ingredient in conjunction with possible exposure to residues of
the inert ingredient in food, drinking water, and other nonoccupational
exposures. 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.
IV. Aggregate Risk Assessment and Determination of Safety
Consistent with section 408(b)(2)(D), EPA has reviewed the
available scientific data and other relevant information in support of
this action. EPA has sufficient data to assess the hazards of polyvinyl
chloride and to make a determination on aggregate exposure, consistent
with section 408(b)(2), for a tolerance exemption for residues on
polyvinyl chloride on growing crops and raw agricultural commodities
after harvest. EPA's assessment of the dietary exposures and risks
associated with establishing these tolerances follows.
The data submitted in the petitions and other relevant material
have been evaluated. As part of the EPA policy statement on inert
ingredients published in the Federal Register of April 22, 1987 (52 FR
13305) (FRL-3190-1), the Agency set forth a list of studies which would
generally be used to evaluate the risks posed by the presence of an
inert ingredient in a pesticide formulation. However, where it can be
determined without that data that the inert ingredient will present
minimal or no risk, the Agency generally does not require some or all
of the listed studies to rule on the proposed tolerance or exemption
from the requirement of a tolerance for an inert ingredient.
A. Toxicological Profile
In the case of certain chemical substances that are defined as
``polymers,'' the Agency has established a set of criteria which
identify categories of polymers that present low risk. These criteria
(described in 40 CFR 723.250) identify polymers that are relatively
unreactive and stable compared to other chemical substances as well as
polymers that typically are not readily absorbed. These properties
generally limit a polymer's ability to cause adverse effects. In
addition, these criteria exclude polymers about which little is known.
The Agency believes that polymers meeting these criteria will present
minimal or no risk. Polyvinyl chloride (PVC) conforms to the definition
of polymer given in 40 CFR 723.250(b) and meets the following criteria
that are used to identify low risk polymers:
1. PVC is not a cationic polymer, nor is it reasonably
anticipated to become a cationic polymer in a natural aquatic
environment.
2. PVC contains as an integral part of its composition the atomic
elements carbon, chlorine, and hydrogen.
3. PVC does not contain as an integral part of its composition,
except as impurities, any elements other than those listed in 40 CFR
section 723.250 (d)(2)(ii).
4. PVC is not designed, nor is it reasonably anticipated to
substantially degrade, decompose, or depolymerize.
5. PVC is not manufactured or imported from monomers and/or other
reactants that are not already included on the Toxic Substance Control
Act (TSCA) Chemical Substance Inventory or manufactured under an
applicable TSCA section 5 exemption.
6. PVC is not a water absorbing polymer.
7. PVC does not contain any group as reactive functional groups.
8. The minimum number-average molecular weight of PVC is listed
as 29,000 daltons. Substances with molecular weights greater than 400
generally are not absorbed through the intact skin, and substances with
molecular weights greater than 1,000 generally are not absorbed through
the intact gastrointestinal (GI) tract. Chemicals not absorbed through
the skin or GI tract generally are incapable of eliciting a toxic
response.
9. PVC has a minimum number-average molecular weight of 29,000
and contains less than 2 percent oligomeric material below molecular
weight 500 and less than 5 percent oligomeric material below 1,000
molecular weight.
In addition, PVC is approved by the Food and Drug Administration
(FDA) under 21 CFR for contact with food as a component in adhesives
(21 CFR 175.105), coatings (21 CFR 175.320), and paper and paperboard
(21 CFR 176.180). PVC is also approved by FDA as an indirect food
additive used as a basic component of acrylic (21 CFR 177.1010) and
cellophane (21 CFR 177.1200) polymers. PVC is also cleared for use as
water pipe for potable water as per FFDCA 201(s).
Based on the conformance of polyvinyl chloride to the above
criteria, no mammalian toxicity is anticipated from dietary, inhalation
or dermal exposure to polyvinyl chloride.
B. Exposures and Risks
1. From food and feed uses, drinking water, and non-dietary
exposures. For the purposes of assessing the potential
[[Page 31644]]
dietary exposure, EPA considered that under this tolerance exemption
polyvinyl chloride could be present in all raw and processed
agricultural commodities and drinking water and that non-occupational,
non-dietary exposure was possible. EPA concluded that, based on this
chemical's categorization as a polymer conforming to the definition of
a polymer under 40 CFR 723.250(b) that also meet the criteria used to
identify low risk polymers, there are no concerns for risks associated
with any potential exposure scenarios that are reasonably foreseeable.
2. Cumulative exposure to substances with common mechanism of
toxicity. Section 408(b)(2)(D)(v) 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.''
In the case of polyvinyl chloride, the lack of expected toxicity of
this substance based on its conformance to the definition of polymers
as given in 40 CFR 723.250(b) as well as the criteria that identify low
risk polymers results in no expected cumulative effects; a cumulative
risk assessment is therefore not necessary.
C. Aggregate Risks and Determination of Safety for U.S. Population
Based on this chemical's conformance to the definition of a polymer
given in 40 CFR 723.250(b) as well as the criteria that are used to
identify low risk polymers, EPA concludes that there is a reasonable
certainty that no harm to the U.S. population will result from
aggregate exposure to polyvinyl chloride. EPA believes this compound
presents no dietary risk under reasonably foreseeable circumstances.
D. Aggregate Risks and Determination of Safety for Infants and Children
FFDCA section 408 provides that EPA shall apply an additional
tenfold margin of safety for infants and children in the case of
threshold effects to account for pre-and postnatal toxicity and the
completeness of the database unless EPA determines that a different
margin of safety will be safe for infants and children. Margins of
safety are incorporated into EPA risk assessments either directly
through use of a MOE analysis or through using uncertainty (safety)
factors in calculating a dose level that poses no appreciable risk to
humans.
Due to the low expected toxicity of polyvinyl chloride, EPA has not
used a safety factor analysis in assessing the risk of this compound.
For the same reasons the additional safety factor is unnecessary.
V. Other Considerations
The Agency proposes to establish an exemption from the requirement
of a tolerance without any numerical limitation; therefore, the Agency
has concluded that analytical methods are not required for enforcement
purposes for polyvinyl chloride.
There are no Codex Alimentarius Commission (Codex), Canadian or
Mexican residue limits for polyvinyl chloride.
VI. Conclusion
Therefore, an exemption from the requirement of a tolerance is
established for residues of polyvinyl chloride.
VII. Objections and Hearing Requests
The new FFDCA section 408(g) provides essentially the same process
for persons to ``object'' to a tolerance regulation issued by EPA under
new section 408(e) and (l)(6) as was provided in the old section 408
and in section 409. However, the period for filing objections is 60
days, rather than 30 days. EPA currently has procedural regulations
which govern the submission of objections and hearing requests. These
regulations will require some modification to reflect the new law.
However, until those modifications can be made, EPA will continue to
use those procedural regulations with appropriate adjustments to
reflect the new law.
Any person may, by August 10, 1998, file written objections to any
aspect of this regulation and may also request a hearing on those
objections. Objections and hearing requests must be filed with the
Hearing Clerk, at the address given above (40 CFR 178.20). A copy of
the objections and/or hearing requests filed with the Hearing Clerk
should be submitted to the OPP docket for this rulemaking. The
objections submitted must specify the provisions of the regulation
deemed objectionable and the grounds for the objections (40 CFR
178.25). Each objection must be accompanied by the fee prescribed by 40
CFR 180.33(i). If a hearing is requested, the objections must include a
statement of the factual issues on which a hearing is requested, the
requestor's contentions on such issues, and a summary of any evidence
relied upon by the requestor (40 CFR 178.27). A request for a hearing
will be granted if the Administrator determines that the material
submitted shows the following: There is 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 in the manner sought by the requestor would be adequate
to justify the action requested (40 CFR 178.32). Information submitted
in connection with an objection or hearing request may be claimed
confidential by marking any part or all of that information as
Confidential Business Information (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.
VIII. Public Record and Electronic Submissions
EPA has established a record for this rulemaking under docket
control number [OPP-300656] (including any comments and data submitted
electronically). A public version of this record, including printed,
paper versions of electronic comments, which does not include any
information claimed as CBI, is available for inspection from 8:30 a.m.
to 4 p.m., Monday through Friday, excluding legal holidays. The public
record is located in Rm. 119 of the Public Information and Records
Integrity Branch, Information Resources and Services Division (7502C),
Office of Pesticide Programs, Environmental Protection Agency, Crystal
Mall #2, 1921 Jefferson Davis Highway, Arlington, VA.
Electronic comments may be sent directly to EPA at:
opp-docket@epamail.epa.gov.
Electronic comments must be submitted as an ASCII file avoiding the
use of special characters and any form of encryption.
The official record for this rulemaking, as well as the public
version, as described above will be kept in paper form. Accordingly,
EPA will transfer any copies of objections and hearing requests
received electronically into printed, paper form as they are received
and will place the paper copies in the official rulemaking record which
will also include all comments submitted directly in writing. The
official rulemaking record is the paper record maintained at the
Virginia address in ``ADDRESSES'' at the beginning of this document.
[[Page 31645]]
IX. Regulatory Assessment Requirements
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). 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) (Pub. L. 104-4). Nor does it require any
prior consultation as specified by Executive Order 12875, entitled
Enhancing the Intergovernmental Partnership (58 FR 58093, October 28,
1993), or special considerations as required by Executive Order 12898,
entitled Federal Actions to Address Environmental Justice in Minority
Populations and Low-Income Populations (59 FR 7629, February 16, 1994),
or require OMB review in accordance with Executive Order 13045,
entitled Protection of Children from Environmental Health Risks and
Safety Risks (62 FR 19885, April 23, 1997).
The Agency has previously assessed whether establishing tolerances,
exemptions from tolerances, raising tolerance levels or expanding
exemptions might adversely impact small entities and concluded, as a
generic matter, that there is no adverse economic impact. The factual
basis for the Agency's generic certification for tolerance actions
published on May 4, 1981 (46 FR 24950) and was provided to the Chief
Counsel for Advocacy of the Small Business Administration.
X. Submission to Congress and the General Accounting Office
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 the rule in the Federal Register. This 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 record
keeping requirements.
Dated: May 21, 1998.
James Jones,
Director, Registration Division, Office of Pesticide Programs.
PART 180 -- [AMENDED]
Therefore, 40 CFR chapter I is amended as follows:
1. The authority citation for part 180 continues to read as
follows:
Authority: 21 U.S.C. 346a and 371.
2. In section 180.1001 the table in paragraph (c) is amended by
adding alphabetically the following inert ingredient to read as
follows:
Sec. 180.1001 Exemption from the requirement of a tolerance.
* * * * *
(c) * * *
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Inert ingredients Limits Uses
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Polyvinyl chloride (CAS Reg. No. ................ Carrier
9002-86-2), minimum number
average molecular weight (in
amu) 29,000.
* * * * * * *
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[FR Doc. 98-15174 Filed 6-9-98; 8:45 am]
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