Health and Safety Data Reporting; Addition of Certain Chemicals, 71561-71567 [2012-28840]
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Federal Register / Vol. 77, No. 232 / Monday, December 3, 2012 / Rules and Regulations
VI. Statutory and Executive Order
Reviews
This final rule establishes tolerances
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this final rule
has been exempted from review under
Executive Order 12866, this final rule is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997). This final rule does not
contain any information collections
subject to OMB approval under the
Paperwork Reduction Act (PRA) (44
U.S.C. 3501 et seq.), nor does it require
any special considerations under
Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the 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.
This final rule directly regulates
growers, food processors, food handlers,
and food retailers, not States or tribes,
nor does this action alter the
relationships or distribution of power
and responsibilities established by
Congress in the preemption provisions
of FFDCA section 408(n)(4). As such,
the Agency has determined that this
action will not have a substantial direct
effect on States or tribal governments,
on the relationship between the national
government and the States or tribal
governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, the Agency has determined
that Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999) and Executive Order 13175,
entitled ‘‘Consultation and Coordination
with Indian Tribal Governments’’ (65 FR
67249, November 9, 2000) do not apply
to this final rule. In addition, this final
rule does not impose any enforceable
duty or contain any unfunded mandate
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as described under Title II of the
Unfunded Mandates Reform Act of 1995
(UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act of 1995
(NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
71561
(2) * * *
Parts per
million
Commodity
*
*
*
*
*
Grass, forage, fodder, and
hay, group 17, forage .........
Grass, forage, fodder, and
hay, group 17, hay ..............
*
Millet,
Millet,
Millet,
Millet,
*
proso,
proso,
proso,
proso,
*
*
*
0.5
*
forage ................
grain ..................
hay ....................
straw .................
*
*
*
20
*
*
*
*
10
0.01
0.01
0.01
*
*
[FR Doc. 2012–29105 Filed 11–30–12; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
Dated: November 21, 2012.
Lois Rossi,
Director, Registration Division, Office of
Pesticide Programs.
40 CFR Part 716
Therefore, 40 CFR chapter I is
amended as follows:
Health and Safety Data Reporting;
Addition of Certain Chemicals
PART 180—[AMENDED]
AGENCY:
[EPA–HQ–OPPT–2011–0363; FRL–9355–9]
RIN 2070–AJ89
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.479 revise the table in
paragraph (a)(1) and add alphabetically
the following new entries to the table in
paragraph (a)(2).
The revised and added text read as
follows:
■
§ 180.479 Halosulfuron-methyl; tolerances
for residues.
(a) * * *
(1) * * *
Parts per
million
Commodity
Cattle, fat ................................
Cattle, meat ............................
Cattle, meat byproducts .........
Goat, fat ..................................
Goat, meat ..............................
Goat, meat byproducts ...........
Hog, meat byproducts ............
Horse, fat ................................
Horse, meat ............................
Horse, meat byproducts .........
Milk .........................................
Sheep, fat ...............................
Sheep, meat ...........................
Sheep, meat byproducts ........
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0.05
0.05
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Environmental Protection
Agency (EPA).
ACTION: Final rule.
This final rule requires
manufacturers (including importers) of
cadmium or cadmium compounds,
including as part of an article, that have
been, or are reasonably likely to be,
incorporated into consumer products to
report certain unpublished health and
safety studies to EPA. The Interagency
Testing Committee (ITC), established
under section 4(e) of the Toxic
Substances Control Act (TSCA) to
recommend chemicals and chemical
mixtures to EPA for priority testing
consideration, amends the TSCA section
4(e) Priority Testing List through
periodic reports submitted to EPA. The
ITC added cadmium and cadmium
compounds to the Priority Testing List
through its 69th ITC Report.
DATES: This final rule is effective
January 2, 2013. For purposes of judicial
review, this final rule shall be
promulgated at 1 p.m. eastern daylight/
standard time on December 17, 2012.
(See 40 CFR 23.5.)
A request to withdraw a chemical
from this final rule pursuant to
§ 716.105(c) must be received on or
SUMMARY:
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before December 17, 2012. (See Unit IV.
of the SUPPLEMENTARY INFORMATION.)
For dates for reporting requirements,
see Unit III.B. of the SUPPLEMENTARY
INFORMATION.
Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2011–0363, by
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
• Mail: Document Control Office
(2822–1T), Office of Chemical Safety
and Pollution Prevention,
Environmental Protection Agency, 1301
Constitution Ave. NW., Washington, DC
20004.
• Hand Delivery: OPPT Document
Control Office (DCO), EPA East Bldg.,
Rm. 6428, 1201 Constitution Ave. NW.,
Washington, DC. ATTN: Docket ID
Number EPA–HQ–OPPT–2011–0363.
The DCO is open from 8 a.m. to 4 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
DCO is (202) 564–8930. Such deliveries
are only accepted during the DCO’s
normal hours of operation, and special
arrangements should be made for
deliveries of boxed information.
Instructions: Direct your comments to
docket ID number EPA–HQ–OPPT–
2011–0363. EPA’s policy is that all
comments received will be included in
the docket without change and may be
made available online at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through regulations.gov or
email. The regulations.gov Web site is
an ‘‘anonymous access’’ system, which
means EPA will not know your identity
or contact information unless you
provide it in the body of your comment.
If you send an email comment directly
to EPA without going through
regulations.gov, your email address will
be automatically captured and included
as part of the comment that is placed in
the docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
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ADDRESSES:
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of encryption, and be free of any defects
or viruses.
Docket: All documents in the docket
are listed in the docket index available
at https://www.regulations.gov. Although
listed in the index, some information is
not publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
will be publicly available only in hard
copy. Publicly available docket
materials are available electronically at
https://www.regulations.gov, or, if only
available in hard copy, at the OPPT
Docket. The OPPT Docket is located in
the EPA Docket Center (EPA/DC) at Rm.
3334, EPA West Bldg., 1301
Constitution Ave. NW., Washington,
DC. The EPA/DC Public Reading Room
hours of operation are 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding
legal holidays. The telephone number of
the EPA/DC Public Reading Room is
(202) 566–1744, and the telephone
number for the OPPT Docket is (202)
566–0280. Docket visitors are required
to show photographic identification,
pass through a metal detector, and sign
the EPA visitor log. All visitor bags are
processed through an X-ray machine
and subject to search. Visitors will be
provided an EPA/DC badge that must be
visible at all times in the building and
returned upon departure.
FOR FURTHER INFORMATION CONTACT:
For technical information contact:
Robert Jones, Chemical Control Division
(7405M), Office of Chemical Safety and
Pollution Prevention, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW., Washington, DC 20460–0001;
telephone number: 202–564–8161;
email address: jones.robert@epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; email address: TSCAHotline@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be affected by this rule if
you are a manufacturer (including
importer) of cadmium or cadmium
compounds, including as part of an
article, that have been, or are reasonably
likely to be, incorporated into consumer
products.
In addition to this final rule, EPA
plans to propose, under a separate
notice and comment rulemaking, to
require the submission of TSCA section
8(d) health and safety studies from
processors and distributors of cadmium
or cadmium compounds, including as
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part of an article, that have been, or are
reasonably likely to be, incorporated
into consumer products to report certain
unpublished health and safety studies to
EPA. The proposed rule will be
published in a subsequent Federal
Register document. As provided in this
rule, health and safety studies regarding
cadmium or cadmium compounds in
articles must be reported, with the
exception of studies not subject to
reporting as described at § 716.20.
While EPA has broad authority to
require submission of health and safety
studies on chemical substances, for the
purposes of this rule EPA has limited
the scope of this rule to those chemical
substances within the listed category
that have been, or are reasonably likely
to be, incorporated into consumer
products, based on EPA’s determination
of what is necessary to carry out the
purposes of TSCA. ‘‘Consumer product’’
is defined in § 716.21(a)(9)(iii) of this
rule to mean ‘‘any product that is sold
or made available to consumers for their
use in or around a permanent or
temporary household or residence, in or
around a school, or in or around
recreational areas.’’ This definition is
based on the definition of ‘‘consumer
use’’ promulgated in 40 CFR 710.43 and
the definition of ‘‘consumer product’’
promulgated in 40 CFR 721.3.
Potentially affected entities may include
but are not limited to:
• Manufacturers of basic inorganic
chemicals (except industrial gases,
inorganic dyes and pigments, alkalis
and chlorine, and carbon black) (NAICS
code 325188).
• Manufacturers (including
importers) of inorganic dyes and
pigments (NAICS code 325131).
• Manufacturers of basic organic
chemical products (except aromatic
petrochemicals, industrial gases,
synthetic organic dyes and pigments,
gum and wood chemicals, cyclic crudes
and intermediates, and ethyl alcohol)
(NAICS code 325199).
• Establishments primarily engaged
in the primary production of nonferrous
metals by smelting ore and/or the
primary refining of nonferrous metals by
electrolytic methods or other processes
(except copper and aluminum) (NAICS
code 331419).
• Establishments engaging in
secondary smelting, refining, and
alloying of nonferrous metal (except
copper and aluminum) (NAICS code
331492).
• Wholesalers of toy and hobby
goods, establishments with product line
12812 (NAICS code 42392).
• Discount department stores (NAICS
code 452112).
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• Warehouse clubs and supercenters
(NAICS code 45291).
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. 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 technical person listed under FOR
FURTHER INFORMATION CONTACT.
B. How do I submit CBI information?
If you wish to claim information
submitted to be CBI, it will be handled
in accordance with procedures set forth
in 40 CFR part 2, subpart B. If you do
not assert a confidentiality claim at the
time of submission, the information may
be made available to the public by EPA
without further notice. See 40 CFR
2.203 (Ref. 1). Do not submit this
information to EPA through
regulations.gov or by email. Clearly
mark the part of the information that
you claim to be CBI. For CBI
information in a disk or CD–ROM that
you mail to EPA, mark the outside of the
disk or CD–ROM as CBI and then
identify electronically within the disk or
CD–ROM the specific information that
is claimed as CBI. Information so
marked will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2 and in § 716.55. Pursuant
to § 716.55, to assert a claim of
confidentiality for information
contained in a submitted record, you
must submit two copies of the
document. One copy must be complete,
and you must indicate what
information, if any, is claimed as
confidential by marking the specific
information on each page with a label
such as ‘‘company confidential,’’
‘‘proprietary,’’ or ‘‘trade secret’’ and
briefly state the basis of the claim. The
second copy must be complete, except
that all the information claimed as CBI
in the first copy must be deleted. The
second copy will be placed in the public
docket. Failure to furnish a second copy
when information is claimed as CBI in
the first copy will be considered a
presumptive waiver of confidentiality.
EPA will notify the respondent by
certified mail that a finding of a
presumptive waiver of the claim of
confidentiality has been made. The
respondent will be given 30 days from
the date of receipt of notification to
submit the required second copy. If the
respondent fails to submit the second
copy within the 30 days, EPA will place
the first copy in the docket.
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II. Background
A. Why is the agency taking this action?
EPA has classified cadmium as a
Group B1, probable human carcinogen
(Ref. 2). Further, EPA has determined
acute (short-term) effects of cadmium in
humans through inhalation exposure
consisting mainly of effects on the lung,
such as pulmonary irritation. Chronic
(long-term) inhalation or oral exposure
to cadmium leads to a build-up of
cadmium in the kidneys which can
cause kidney disease. Cadmium has
been shown to be a developmental
toxicant in animals, resulting in fetal
malformations and other effects, but no
conclusive evidence exists in humans.
Animal studies have demonstrated an
increase in lung cancer from long-term
inhalation exposure to cadmium (Refs.
2–4). Due to the potential health effects
of exposure to cadmium or cadmium
compounds, EPA and the Consumer
Product Safety Commission (CPSC) are
concerned about the possible presence
and bioavailability of cadmium or
cadmium compounds in consumer
products generally and especially those
consumer products used by or around
children (Ref. 5).
B. What action is the agency taking?
EPA is issuing a final TSCA section
8(d) rule under procedures in the Health
and Safety Data Reporting rule, 40 CFR
part 716, to require manufacturers
(including importers) of cadmium or
cadmium compounds, including as part
of an article, that have been, or are
reasonably likely to be, incorporated
into consumer products to submit
certain unpublished health and safety
studies to EPA.
EPA has reviewed CPSC’s recalls of
cadmium-contaminated children’s
products. Most of the recalled products
were produced abroad and imported
from other countries (Ref. 6). Based in
part on this information, EPA expects to
capture health and safety studies
conducted by importers of such
products through this final rule. These
parties are located primarily in the
United States and may be subject to
CPSC certification requirements and,
depending on the product, may be
conducting testing using Standard
Consumer Safety Specification for Toy
Safety, ASTM International (ASTM) F–
963 (Ref. 7).
The regulatory text of this final rule
lists the category cadmium and
cadmium compounds. The regulatory
text also lists the data reporting
requirements imposed by this
amendment to the TSCA section 8(d)
model rule.
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71563
C. What is the agency’s authority?
Section 8(d) of TSCA authorizes EPA
to require ‘‘any person who
manufactures, processes, or distributes
in commerce or who proposes to
manufacture, process, or distribute in
commerce, any chemical substance or
mixture’’ to submit lists of health and
safety studies conducted or initiated by
or for such person with respect to such
substance or mixture at any time,
known to such person, or reasonably
ascertainable by such person; and
copies of any study contained on a list
submitted pursuant to section (8)(d)(1)
of TSCA or otherwise known by such
person. Under TSCA section 3(7),
import is included in the definition of
‘‘manufacture.’’
The term health and safety study
should be interpreted broadly and is
defined in § 716.3.
Since the TSCA section 8(d) model
rule is codified in 40 CFR part 716, EPA
uses this TSCA section 8(d) model rule
to quickly gather information on
chemical substances. The TSCA section
8(d) model rule requires past, current,
and prospective manufacturers
(including importers) and (if specified
by EPA in a particular rule or notice
under TSCA section 8(d)) processors to
submit to EPA copies and lists of health
and safety studies on the listed chemical
substances that they manufacture,
import, or process. These studies
provide EPA with useful information
and have provided significant support
for EPA’s decisionmaking under TSCA
sections 4, 5, 6, 8, and 9.
The TSCA section 8(d) model rule
provides for the addition of TSCA
section 4(e) Priority Testing List
chemical substances or categories of
chemical substances. EPA s amending
the TSCA section 8(d) model rule by
adding the recommended category of
chemical substances consistent with
§ 716.105(b) and (c). In doing so, EPA
must provide a 14-day period, which
starts upon publication of the
amendments to the TSCA section 8(d)
model rule in the Federal Register, for
persons to submit information showing
why a chemical substance, mixture, or
category of chemical substances should
be withdrawn from the amendment. The
amendment adding these chemical
substances to the TSCA section 8(d)
model rule is effective 30 days after date
of publication in the Federal Register. If
the EPA Administrator withdraws a
chemical substance from the
amendment, then no later than 30 days
after the date of publication of the
amendment in the Federal Register, a
Federal Register document announcing
this decision will publish.
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D. Why is this action being issued as a
final rule?
B. What are the general reporting
requirements and deadlines?
EPA is publishing this action as a
final rule pursuant to the procedures set
forth in § 716.105(b) and (c). EPA finds
that there is ‘‘good cause’’ under the
Administrative Procedure Act (APA) (5
U.S.C. 553(b)(3)(B)) to make these
amendments without prior notice and
comment. EPA believes notice and an
opportunity for comment on this action
are unnecessary. TSCA directs the ITC
to add chemical substances to the
Priority Testing List for which EPA
should give priority consideration. EPA
also lacks the authority to remove a
chemical substance from the Priority
Testing List once it has been added by
the ITC. As explained earlier in this
preamble, pursuant to § 716.105(b) and
(c), once the ITC adds a chemical
substance to the Priority Testing List,
EPA adds that chemical substance to the
list of chemical substances subject to the
TSCA section 8(d) model rule reporting
requirements, unless the ITC designated
and recommended more than 50
chemical substances or categories of
chemical substances in a calendar year
or EPA withdraws the chemical
substance from the TSCA section 8(d)
model rule for good cause. EPA
promulgated this procedure in 1985
after having solicited public comment
on the need for and mechanics of this
procedure (Ref. 8). Because that rule
established the procedure for adding
ITC chemical substances to the TSCA
section 8(d) model rule, it is
unnecessary to request comment on the
procedure in this action. Finally,
§ 716.105(b) and (c) do provide EPA
with the discretion to withdraw a
chemical substance from the TSCA
section 8(d) model rule for good cause,
including if a party submits to EPA
information showing good cause that a
chemical substance should be removed
from the TSCA section 8(d) model rule.
This final rule, issued pursuant to
TSCA section 8(d) and its regulations,
requires manufacturers (including
importers) of cadmium or cadmium
compounds, including as part of an
article, that have been, or are reasonably
likely to be, incorporated into consumer
products to report certain unpublished
health and safety studies to EPA. Listed
in this unit are the reporting
requirements for the chemical
substances being added by this action to
the TSCA section 8(d) model rule.
The following types of persons need
to report:
1. Persons who, in the 10 years
preceding the date a chemical substance
is listed at § 716.120, either have
proposed to manufacture or import or
have manufactured or imported the
listed substance must submit to EPA,
during the 60-day reporting period
specified in § 716.65 and according to
the reporting schedule set forth at
§ 716.60, a copy of each health and
safety study which is in their possession
at the time the chemical substance is
listed.
2. Persons who, at the time the
chemical substance is listed, propose to
manufacture or import, or are
manufacturing or importing the listed
chemical substance must submit to EPA
during the 60-day reporting period
specified in § 716.65 and according to
the reporting schedule set forth at
§ 716.60:
i. A copy of each health and safety
study which is in their possession at the
time the chemical substance is listed.
ii. A list of the health and safety
studies known to them but not in their
possession at the time the chemical
substance is listed.
iii. A list of the health and safety
studies that are ongoing at the time the
chemical substance is listed and are
being conducted by or for them.
iv. A list of the health and safety
studies that are initiated after the date
the chemical substance is listed and will
be conducted by or for them.
v. A list of unpublished studies which
have been sent to a Federal agency with
no claims of confidentiality or copies of
each such study.
vi. A copy of each health and safety
study that was previously listed as
ongoing or subsequently initiated (i.e.,
listed in accordance with reporting
requirements described at Unit
III.B.2.iii. and iv. respectively) when
complete—regardless of completion
date.
3. Persons who, after the time the
substance is listed, propose to
III. Final Rule
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A. What chemicals are to be added?
EPA is adding the category of
cadmium and cadmium compounds to
the TSCA section 8(d) model rule as
requested by the ITC in the 69th ITC
Report (Ref. 9). This final rule requires
manufacturers (including importers) of
cadmium or cadmium compounds,
including as part of an article, that have
been, or are reasonably likely to be,
incorporated into consumer products to
report certain unpublished health and
safety studies to EPA.
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manufacture or import the listed
chemical substance must submit to EPA
during the reporting period specified in
§ 716.65 and according to the reporting
schedule set forth at § 716.60:
i. A copy of each health and safety
study which is in their possession at the
time they propose to manufacture or
import the listed chemical substance.
ii. A list of the health and safety
studies known to them but not in their
possession at the time they propose to
manufacture or import the listed
chemical substance.
iii. A list of the health and safety
studies that are ongoing at the time they
propose to manufacture or import the
listed chemical substance, and are being
conducted by or for them.
iv. A list of the health and safety
studies that are initiated after the time
they propose to manufacture or import
the listed chemical substance, and will
be conducted by or for them.
v. A list of unpublished studies which
have been sent to a Federal agency with
no claims of confidentiality or copies of
each such study.
vi. A copy of each health and safety
study that was previously listed as
ongoing or subsequently initiated (i.e.,
listed in accordance with reporting
requirements described in Unit
III.B.3.iii. and iv. respectively) when
complete—regardless of the completion
date.
Generally, the reporting described in
Unit III.B. is required by March 4, 2013.
Any person who manufactures or
imports, or who proposes to
manufacture or import, the listed
chemical substance as described in Unit
III.B. from January 2, 2013 to March 4,
2013 must inform EPA by submitting a
list of any studies initiated during the
period from January 2, 2013 to March 4,
2013 within 30 days of their initiation,
but in no case later than April 2, 2013.
In addition, if any such person has
submitted lists of studies that were
ongoing or initiated during the period
from January 2, 2013 to March 4, 2013
to EPA, such person must submit a copy
of each study within 30 days after its
completion, regardless of the study’s
completion date. See §§ 716.60 and
716.65.
Detailed requirements for reporting
unpublished health and safety studies
are published in 40 CFR part 716. Also
found there are explanations of the
reporting exemptions.
C. What are the chemical specific
reporting requirements?
Pursuant to § 716.20(b)(5), the types of
health, and/or environmental effects
studies that need to be reported and the
chemical substance grade/purity
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requirements that need to be met or
exceeded in individual studies for
cadmium and cadmium compounds are
as follows:
1. For the category ‘‘cadmium and
cadmium compounds’’ (defined as
compounds including any unique
chemical substance that contains
cadmium as part of that chemical’s
structure), reporting would extend to all
unpublished health and safety studies
generally reportable under §§ 716.10
and 716.20, for example but not limited
to those that:
i. Relate to the cadmium content
(either from cadmium or cadmium
compounds) of consumer products
(including the specific cadmium
compound (defined in Unit III.A.) used
in the products such as surface coatings
and filler), data related to the product
formulations, and function of the
cadmium (e.g., stabilizer, colorant, etc.)
in the products.
ii. Relate to the assessment of
consumer exposure to cadmium from
such products (including studies of
bioavailability, description of the
consumer use (e.g., paints used on
plastics), physical form of the product
containing cadmium, method of
consumer product application (e.g.,
spray applied, etc.), number of
potentially exposed consumers).
iii. Include data on cadmium
migration from products (e.g.,
conducted using acid extraction or
saline solution tests).
iv. Include bio-monitoring data on
cadmium presence in tissues.
v. Focus on route, duration, and
frequency of exposure to cadmium in
products.
vi. Provide toxicity data on cadmium
or cadmium compounds including in
vitro, in vivo, epidemiological,
computational, or other studies on
effects of exposure to or use of the
cadmium-containing product, material,
or component.
vii. Discuss the function or use of
cadmium or cadmium compounds in a
product, material or component
including typical concentration.
viii. Include data conducted in
compliance with ASTM certification
standards and studies focusing on the
effects of the cadmium or cadmium
compounds in consumer products on
the health and safety of children.
2. With regard to purity, studies
showing any measurable content of
cadmium or cadmium compounds must
be submitted.
D. What are the economic implications
of this action?
EPA’s economic analysis for the
addition of cadmium and cadmium
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compounds to the Health and Safety
Data Reporting rule is entitled ‘‘TSCA
Section 8(d): Economic Impact Analysis
for the Addition of Manufacturers and
Importers of Consumer Products
Containing Cadmium and Cadmium
Compounds From the Sixty-Ninth
Report of the TSCA Interagency Testing
Committee to the Health and Safety Data
Reporting Rule’’ (Ref. 10), and can be
found in the docket for this rule.
EPA has estimated that 1,384 firms
are subject to the rule and that 28 firms
will have relevant studies to submit to
EPA. EPA believes firms that are subject
to the rule will need to perform various
activities in order to comply with its
requirements. The estimated cost of this
TSCA section 8(d) rule to firms is
approximately $481,000.
The estimated cost of this TSCA
section 8(d) rule to the Federal
Government is approximately the time
of 300 hours. That will amount to a cost
to the Federal Government of
approximately $23,500.
IV. Requesting a Chemical Substance
Be Withdrawn From the Final Rule
As specified in § 716.105(c), EPA may
remove a chemical substance or
category of chemical substances from
this final rule for good cause prior to the
effective date of this final rule. Any
person who believes that the reporting
required by this final rule is not
warranted for a chemical substance, or
the category of chemical substances
listed in this final rule may submit to
EPA reasons for that belief. You must
submit your request to EPA on or before
December 17, 2012 and in accordance
with the instructions provided in
§ 716.105(c) and (d), which are briefly
summarized here. In addition, to ensure
proper receipt by EPA, you should
identify docket ID number EPA–HQ–
OPPT–2011–0363 on your request and
must submit that request in accordance
with the instructions in § 716.105(c) and
(d). If the Assistant Administrator,
Office of Chemical Safety and Pollution
Prevention, withdraws a chemical
substance or the category of chemical
substances from this TSCA section 8(d)
amendment, in accordance with
§ 716.105(c), a Federal Register
document announcing this decision will
be published no later than January 2,
2013.
V. References
The docket for this final rule has been
established under docket ID number
EPA–HQ–OPPT–2011–0363. The docket
is available for review as specified in
ADDRESSES. The following is a listing of
the documents referenced in this
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preamble that have been placed in the
docket for this final rule:
1. EPA. Requests for Information;
Confidentiality of Business Information;
Final Rule. Federal Register (41 FR 36902,
September 1, 1976).
2. EPA. Integrated Risk Information
System. Cadmium (CASRN 7440–43–9) IRIS
Summary. June 1992. Available online at:
https://www.epa.gov/iris/subst/0141.htm.
3. Agency for Toxic Substances and
Disease Registry (ATSDR), U.S. Department
of Health and Human Services (HHS).
ATSDR Toxicological Profile for Cadmium
(Draft). September 2008. Available online at:
https://www.atsdr.cdc.gov/toxprofiles/
tp.asp?id=48&tid=15.
4. Technology Transfer Network Air Toxics
Web Site, Cadmium Compounds (A). January
2000. Available online at: https://epa.gov/ttn/
atw/hlthef/cadmium.html.
5. ITC. Sixty-Eighth Report of the TSCA
Interagency Testing Committee to the
Administrator of the Environmental
Protection Agency; Receipt of Report and
Request for Comments; Notice. Federal
Register (76 FR 46174, August 1, 2011) (FRL–
8879–3). Available online at: https://
www.gpo.gov/fdsys/pkg/FR-2011-08-01/pdf/
2011-19414.pdf.
6. CPSC. Recalls and Product Safety News.
Available online at: https://www.cpsc.gov/cgibin/haz.aspx and select ‘‘Cadmium.’’
7. Standard Consumer Safety Specification
for Toy Safety, ASTM F–963. Available
online at:
https://www.astm.org/Standards/F963.htm
and also available online at: https://
www.regulations.gov in docket ID number
EPA–HQ–OPPT–2011–0363.
8. EPA. Chemical Information Rules;
Additional Automatic Reporting; Final Rule.
Federal Register (50 FR 34809, August 28,
1985).
9. ITC. Sixty-Ninth Report of the TSCA
Interagency Testing Committee to the
Administrator of the Environmental
Protection Agency; Receipt of Report and
Request for Comments; Notice. Federal
Register (77 FR 30856, May 23, 2012) (FRL–
9346–3). Available online at: https://
www.gpo.gov/fdsys/pkg/FR-2012-05-23/pdf/
2012-12493.pdf.
10. EPA. TSCA Section 8(d): Economic
Impact Analysis for the Addition of
Manufacturers and Importers of Consumer
Products Containing Cadmium and Cadmium
Compounds From the Sixty-Ninth Report of
the TSCA Interagency Testing Committee to
the Health and Safety Data Reporting Rule.
May 14, 2012.
VI. Statutory and Executive Order
Reviews
A. Regulatory Planning and Review
Under Executive Order 12866 (58 FR
51735, October 4, 1993), entitled
‘‘Regulatory Planning and Review,’’ this
action is not a ‘‘significant regulatory
action’’ and was therefore not reviewed
by the Office of Management and
Budget (OMB) under Executive Orders
12866 and 13563, entitled ‘‘Improving
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Regulation and Regulatory Review’’ (76
FR 3821, January 21, 2011).
B. Paperwork Reduction Act
The information collection
requirements contained in TSCA section
8(d) model rules have already been
approved by OMB under the provisions
of the Paperwork Reduction Act (PRA),
44 U.S.C. 3501 et seq., and OMB control
number 2070–0004 (EPA ICR No. 0575).
The collection activities in this final
rule are captured by the existing
approval and do not require additional
review and/or approval by OMB.
EPA estimates that the information
collection activities related to health
and safety data reporting for the
category of cadmium and cadmium
compounds in this final rule will result
in a total public reporting burden of
7,019 hours. Of that total, an estimated
2,768 hours are estimated to be spent
performing an initial review of the final
rule. The remaining hours are associated
with the actual required reporting
activities (Ref. 10). As defined by PRA
and 5 CFR 1320.3(b), ‘‘burden’’ means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, or disclose or
provide information to or for a Federal
agency. This includes the time needed
to: Review instructions; develop,
acquire, install, and utilize technology
and systems for the purposes of
collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements which have subsequently
changed; train personnel to be able to
respond to a collection of information;
search data sources; complete and
review the collection of information;
and transmit or otherwise disclose the
information.
Under PRA, an agency may not
conduct or sponsor, and a person is not
required to respond to, an information
collection request unless it displays a
currently valid OMB control number.
The OMB control numbers for EPA’s
regulations, including its regulations
implementing TSCA section 8(d) at 40
CFR part 716, are listed in the table in
40 CFR part 9 and included on the
related collection instrument. This
listing of the OMB control numbers and
their subsequent codification in the CFR
satisfies the display requirements of
PRA and OMB’s implementing
regulations at 5 CFR part 1320.
C. Regulatory Flexibility Act
This final rule is not subject to the
Regulatory Flexibility Act (RFA), which
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generally requires an agency to prepare
a regulatory flexibility analysis for any
rule that will have a significant
economic impact on a substantial
number of small entities. RFA applies
only to rules subject to notice and
comment rulemaking requirements
under the Administrative Procedure Act
(APA) or any other statute. This rule is
not subject to notice and comment
requirements under the APA or any
other statute because although the rule
is subject to the APA, the Agency has
invoked the ‘‘good cause’’ exemption
under 5 U.S.C. 553(b)(3)(B), therefore it
is not subject to the notice and comment
requirement.
D. Unfunded Mandates Reform Act
Pursuant to Title II of the Unfunded
Mandates Reform Act, 2 U.S.C. 1531–
1538, EPA has determined that this final
rule does not contain a Federal mandate
that may result in expenditures of $100
million or more for State, local, and
tribal governments, in the aggregate, or
the private sector in any 1 year. In
addition, EPA has determined that this
final rule will not significantly or
uniquely affect small governments.
Accordingly, the final rule is not subject
to the requirements of UMRA sections
202, 203, 204, or 205.
E. Federalism
Under Executive Order 13132,
entitled ‘‘Federalism’’ (64 FR 43255,
August 10, 1999), EPA has determined
that this final rule does not have
federalism implications because it will
not 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, as specified in the
Executive Order. The rule establishes
reporting requirements that apply to
manufacturers (including importers) of a
category of cadmium and cadmium
compounds. The requirements of this
final rule are not expected to apply to
States and localities and would not
affect State and local governments.
F. Indian Tribal Governments
This action will not have tribal
implications as specified in Executive
Order 13175, entitled ‘‘Consultation and
Coordination With Indian Tribal
Governments’’ (65 FR 67249, November
9, 2000). EPA has determined that this
final rule will not have tribal
implications because it will not have
substantial direct effects on tribal
governments, on the relationship
between the Federal Government and
the Indian tribes, or on the distribution
of power and responsibilities between
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the Federal Government and Indian
tribes, as specified in the Executive
Order. EPA has no information to
indicate that any tribal government
manufactures or imports the chemical
substances covered by this action.
G. Protection of Children
This action is not subject to Executive
Order 13045, entitled ‘‘Protection of
Children From Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997), because this action is
not an economically significant
regulatory action as defined by
Executive Order 12866. However,
cadmium and cadmium compounds are
used in toys that are intended for use by
children, and thus presents a
disproportionate risk to children. The
agency adequately considered children’s
health issues during rule development.
H. Effect on Energy Supply, Distribution,
or Use
This action is not a ‘‘significant
energy action’’ as defined in Executive
Order 13211, entitled ‘‘Actions
Concerning Regulations That
Significantly Affect Energy Supply
Distribution’’ (66 FR 28355, May 22,
2001), because this action is not an
economically significant regulatory
action as defined by Executive Order
12866, and it is not likely to have a
significant adverse effect on the supply,
distribution, or use of energy.
I. Technical Standards
Because this action will not involve
any technical standards, section 12(d) of
the National Technology Transfer and
Advancement Act, 15 U.S.C. 272 note,
does not apply to this action.
J. Environmental Justice
This action does not entail special
considerations of environmental justice
related issues as delineated by
Executive Order 12898, entitled
‘‘Federal Actions To Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994). This action is expected to have a
positive impact on children in lowincome and minority communities by
increasing the amount of cadmium
health and safety data available to EPA
and consumers.
VII. Congressional Review Act
Pursuant to the Congressional Review
Act, 5 U.S.C. 801 et seq., EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
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publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
2. In § 716.21, add new paragraph
(a)(9) to read as follows:
■
List of Subjects in 40 CFR Part 716
Environmental protection, Chemicals,
Hazardous substances, Health and safety
studies, Reporting and recordkeeping
requirements.
Dated: November 20, 2012.
Wendy C. Hamnett,
Director, Office of Pollution Prevention and
Toxics.
Therefore, 40 CFR chapter I is
amended as follows:
PART 716—[AMENDED]
1. The authority citation for part 716
continues to read as follows:
■
Authority: 15 U.S.C. 2607(d).
*
*
Cadmium and cadmium compounds
(any unique chemical substance that
contains cadmium as part of that
chemical’s structure).
Manufacturers (including importers) ......
*
*
*
*
*
(a) * * *
(9) (i) Reporting requirements for the
category ‘‘cadmium and cadmium
compounds’’ apply only to persons that
manufacture (including import)
cadmium or cadmium compounds that
have been, or are reasonably likely to be,
incorporated into consumer products.
(A) All unpublished health and safety
studies generally reportable under 40
CFR 716.10 and 716.20 must be
reported.
(B) [Reserved]
(ii) With regard to purity, studies
showing any measurable content of
cadmium or cadmium compounds in
such products must be reported.
§ 716.120 Substances and listed mixtures
to which this subpart applies.
*
*
*
(c) * * *
CAS No.
(examples for
category)
Category
*
§ 716.21 Chemical specific reporting
requirements.
(iii) For the purposes of this
paragraph (a)(9), consumer product
means any product that is sold or made
available to consumers for their use in
or around a permanent or temporary
household or residence, in or around a
school, or in or around recreational
areas.
*
*
*
*
*
3. In § 716.120, add, before the entry
‘‘Chlorinated benzenes, mono-, di-, tri-,
tetra-, and penta-,’’ the category
‘‘Cadmium and cadmium compounds’’
and its entry in alphabetical order to the
table in paragraph (c) to read as follows:
Special
exemptions
Effective date
*
................
*
................................
*
January 2, 2013 .........................
................
§ 716.21(a)(9)
*
*
*
March 4, 2013.
*
*
*
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Agencies
[Federal Register Volume 77, Number 232 (Monday, December 3, 2012)]
[Rules and Regulations]
[Pages 71561-71567]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-28840]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 716
[EPA-HQ-OPPT-2011-0363; FRL-9355-9]
RIN 2070-AJ89
Health and Safety Data Reporting; Addition of Certain Chemicals
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule requires manufacturers (including importers)
of cadmium or cadmium compounds, including as part of an article, that
have been, or are reasonably likely to be, incorporated into consumer
products to report certain unpublished health and safety studies to
EPA. The Interagency Testing Committee (ITC), established under section
4(e) of the Toxic Substances Control Act (TSCA) to recommend chemicals
and chemical mixtures to EPA for priority testing consideration, amends
the TSCA section 4(e) Priority Testing List through periodic reports
submitted to EPA. The ITC added cadmium and cadmium compounds to the
Priority Testing List through its 69th ITC Report.
DATES: This final rule is effective January 2, 2013. For purposes of
judicial review, this final rule shall be promulgated at 1 p.m. eastern
daylight/standard time on December 17, 2012. (See 40 CFR 23.5.)
A request to withdraw a chemical from this final rule pursuant to
Sec. 716.105(c) must be received on or
[[Page 71562]]
before December 17, 2012. (See Unit IV. of the SUPPLEMENTARY
INFORMATION.)
For dates for reporting requirements, see Unit III.B. of the
SUPPLEMENTARY INFORMATION.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2011-0363, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments.
Mail: Document Control Office (2822-1T), Office of
Chemical Safety and Pollution Prevention, Environmental Protection
Agency, 1301 Constitution Ave. NW., Washington, DC 20004.
Hand Delivery: OPPT Document Control Office (DCO), EPA
East Bldg., Rm. 6428, 1201 Constitution Ave. NW., Washington, DC. ATTN:
Docket ID Number EPA-HQ-OPPT-2011-0363. The DCO is open from 8 a.m. to
4 p.m., Monday through Friday, excluding legal holidays. The telephone
number for the DCO is (202) 564-8930. Such deliveries are only accepted
during the DCO's normal hours of operation, and special arrangements
should be made for deliveries of boxed information.
Instructions: Direct your comments to docket ID number EPA-HQ-OPPT-
2011-0363. EPA's policy is that all comments received will be included
in the docket without change and may be made available online at https://www.regulations.gov, including any personal information provided,
unless the comment includes information claimed to be Confidential
Business Information (CBI) or other information whose disclosure is
restricted by statute. Do not submit information that you consider to
be CBI or otherwise protected through regulations.gov or email. The
regulations.gov Web site is an ``anonymous access'' system, which means
EPA will not know your identity or contact information unless you
provide it in the body of your comment. If you send an email comment
directly to EPA without going through regulations.gov, your email
address will be automatically captured and included as part of the
comment that is placed in the docket and made available on the
Internet. If you submit an electronic comment, EPA recommends that you
include your name and other contact information in the body of your
comment and with any disk or CD-ROM you submit. If EPA cannot read your
comment due to technical difficulties and cannot contact you for
clarification, EPA may not be able to consider your comment. Electronic
files should avoid the use of special characters, any form of
encryption, and be free of any defects or viruses.
Docket: All documents in the docket are listed in the docket index
available at https://www.regulations.gov. Although listed in the index,
some information is not publicly available, e.g., CBI or other
information whose disclosure is restricted by statute. Certain other
material, such as copyrighted material, will be publicly available only
in hard copy. Publicly available docket materials are available
electronically at https://www.regulations.gov, or, if only available in
hard copy, at the OPPT Docket. The OPPT Docket is located in the EPA
Docket Center (EPA/DC) at Rm. 3334, EPA West Bldg., 1301 Constitution
Ave. NW., Washington, DC. The EPA/DC Public Reading Room hours of
operation are 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding
legal holidays. The telephone number of the EPA/DC Public Reading Room
is (202) 566-1744, and the telephone number for the OPPT Docket is
(202) 566-0280. Docket visitors are required to show photographic
identification, pass through a metal detector, and sign the EPA visitor
log. All visitor bags are processed through an X-ray machine and
subject to search. Visitors will be provided an EPA/DC badge that must
be visible at all times in the building and returned upon departure.
FOR FURTHER INFORMATION CONTACT:
For technical information contact: Robert Jones, Chemical Control
Division (7405M), Office of Chemical Safety and Pollution Prevention,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460-0001; telephone number: 202-564-8161; email
address: jones.robert@epa.gov.
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; email address: TSCA-Hotline@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be affected by this rule if you are a manufacturer
(including importer) of cadmium or cadmium compounds, including as part
of an article, that have been, or are reasonably likely to be,
incorporated into consumer products.
In addition to this final rule, EPA plans to propose, under a
separate notice and comment rulemaking, to require the submission of
TSCA section 8(d) health and safety studies from processors and
distributors of cadmium or cadmium compounds, including as part of an
article, that have been, or are reasonably likely to be, incorporated
into consumer products to report certain unpublished health and safety
studies to EPA. The proposed rule will be published in a subsequent
Federal Register document. As provided in this rule, health and safety
studies regarding cadmium or cadmium compounds in articles must be
reported, with the exception of studies not subject to reporting as
described at Sec. 716.20.
While EPA has broad authority to require submission of health and
safety studies on chemical substances, for the purposes of this rule
EPA has limited the scope of this rule to those chemical substances
within the listed category that have been, or are reasonably likely to
be, incorporated into consumer products, based on EPA's determination
of what is necessary to carry out the purposes of TSCA. ``Consumer
product'' is defined in Sec. 716.21(a)(9)(iii) of this rule to mean
``any product that is sold or made available to consumers for their use
in or around a permanent or temporary household or residence, in or
around a school, or in or around recreational areas.'' This definition
is based on the definition of ``consumer use'' promulgated in 40 CFR
710.43 and the definition of ``consumer product'' promulgated in 40 CFR
721.3. Potentially affected entities may include but are not limited
to:
Manufacturers of basic inorganic chemicals (except
industrial gases, inorganic dyes and pigments, alkalis and chlorine,
and carbon black) (NAICS code 325188).
Manufacturers (including importers) of inorganic dyes and
pigments (NAICS code 325131).
Manufacturers of basic organic chemical products (except
aromatic petrochemicals, industrial gases, synthetic organic dyes and
pigments, gum and wood chemicals, cyclic crudes and intermediates, and
ethyl alcohol) (NAICS code 325199).
Establishments primarily engaged in the primary production
of nonferrous metals by smelting ore and/or the primary refining of
nonferrous metals by electrolytic methods or other processes (except
copper and aluminum) (NAICS code 331419).
Establishments engaging in secondary smelting, refining,
and alloying of nonferrous metal (except copper and aluminum) (NAICS
code 331492).
Wholesalers of toy and hobby goods, establishments with
product line 12812 (NAICS code 42392).
Discount department stores (NAICS code 452112).
[[Page 71563]]
Warehouse clubs and supercenters (NAICS code 45291).
This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. 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 technical person listed under FOR FURTHER
INFORMATION CONTACT.
B. How do I submit CBI information?
If you wish to claim information submitted to be CBI, it will be
handled in accordance with procedures set forth in 40 CFR part 2,
subpart B. If you do not assert a confidentiality claim at the time of
submission, the information may be made available to the public by EPA
without further notice. See 40 CFR 2.203 (Ref. 1). Do not submit this
information to EPA through regulations.gov or by email. Clearly mark
the part of the information that you claim to be CBI. For CBI
information in a disk or CD-ROM that you mail to EPA, mark the outside
of the disk or CD-ROM as CBI and then identify electronically within
the disk or CD-ROM the specific information that is claimed as CBI.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2 and in Sec. 716.55. Pursuant to
Sec. 716.55, to assert a claim of confidentiality for information
contained in a submitted record, you must submit two copies of the
document. One copy must be complete, and you must indicate what
information, if any, is claimed as confidential by marking the specific
information on each page with a label such as ``company confidential,''
``proprietary,'' or ``trade secret'' and briefly state the basis of the
claim. The second copy must be complete, except that all the
information claimed as CBI in the first copy must be deleted. The
second copy will be placed in the public docket. Failure to furnish a
second copy when information is claimed as CBI in the first copy will
be considered a presumptive waiver of confidentiality. EPA will notify
the respondent by certified mail that a finding of a presumptive waiver
of the claim of confidentiality has been made. The respondent will be
given 30 days from the date of receipt of notification to submit the
required second copy. If the respondent fails to submit the second copy
within the 30 days, EPA will place the first copy in the docket.
II. Background
A. Why is the agency taking this action?
EPA has classified cadmium as a Group B1, probable human carcinogen
(Ref. 2). Further, EPA has determined acute (short-term) effects of
cadmium in humans through inhalation exposure consisting mainly of
effects on the lung, such as pulmonary irritation. Chronic (long-term)
inhalation or oral exposure to cadmium leads to a build-up of cadmium
in the kidneys which can cause kidney disease. Cadmium has been shown
to be a developmental toxicant in animals, resulting in fetal
malformations and other effects, but no conclusive evidence exists in
humans. Animal studies have demonstrated an increase in lung cancer
from long-term inhalation exposure to cadmium (Refs. 2-4). Due to the
potential health effects of exposure to cadmium or cadmium compounds,
EPA and the Consumer Product Safety Commission (CPSC) are concerned
about the possible presence and bioavailability of cadmium or cadmium
compounds in consumer products generally and especially those consumer
products used by or around children (Ref. 5).
B. What action is the agency taking?
EPA is issuing a final TSCA section 8(d) rule under procedures in
the Health and Safety Data Reporting rule, 40 CFR part 716, to require
manufacturers (including importers) of cadmium or cadmium compounds,
including as part of an article, that have been, or are reasonably
likely to be, incorporated into consumer products to submit certain
unpublished health and safety studies to EPA.
EPA has reviewed CPSC's recalls of cadmium-contaminated children's
products. Most of the recalled products were produced abroad and
imported from other countries (Ref. 6). Based in part on this
information, EPA expects to capture health and safety studies conducted
by importers of such products through this final rule. These parties
are located primarily in the United States and may be subject to CPSC
certification requirements and, depending on the product, may be
conducting testing using Standard Consumer Safety Specification for Toy
Safety, ASTM International (ASTM) F-963 (Ref. 7).
The regulatory text of this final rule lists the category cadmium
and cadmium compounds. The regulatory text also lists the data
reporting requirements imposed by this amendment to the TSCA section
8(d) model rule.
C. What is the agency's authority?
Section 8(d) of TSCA authorizes EPA to require ``any person who
manufactures, processes, or distributes in commerce or who proposes to
manufacture, process, or distribute in commerce, any chemical substance
or mixture'' to submit lists of health and safety studies conducted or
initiated by or for such person with respect to such substance or
mixture at any time, known to such person, or reasonably ascertainable
by such person; and copies of any study contained on a list submitted
pursuant to section (8)(d)(1) of TSCA or otherwise known by such
person. Under TSCA section 3(7), import is included in the definition
of ``manufacture.''
The term health and safety study should be interpreted broadly and
is defined in Sec. 716.3.
Since the TSCA section 8(d) model rule is codified in 40 CFR part
716, EPA uses this TSCA section 8(d) model rule to quickly gather
information on chemical substances. The TSCA section 8(d) model rule
requires past, current, and prospective manufacturers (including
importers) and (if specified by EPA in a particular rule or notice
under TSCA section 8(d)) processors to submit to EPA copies and lists
of health and safety studies on the listed chemical substances that
they manufacture, import, or process. These studies provide EPA with
useful information and have provided significant support for EPA's
decisionmaking under TSCA sections 4, 5, 6, 8, and 9.
The TSCA section 8(d) model rule provides for the addition of TSCA
section 4(e) Priority Testing List chemical substances or categories of
chemical substances. EPA s amending the TSCA section 8(d) model rule by
adding the recommended category of chemical substances consistent with
Sec. 716.105(b) and (c). In doing so, EPA must provide a 14-day
period, which starts upon publication of the amendments to the TSCA
section 8(d) model rule in the Federal Register, for persons to submit
information showing why a chemical substance, mixture, or category of
chemical substances should be withdrawn from the amendment. The
amendment adding these chemical substances to the TSCA section 8(d)
model rule is effective 30 days after date of publication in the
Federal Register. If the EPA Administrator withdraws a chemical
substance from the amendment, then no later than 30 days after the date
of publication of the amendment in the Federal Register, a Federal
Register document announcing this decision will publish.
[[Page 71564]]
D. Why is this action being issued as a final rule?
EPA is publishing this action as a final rule pursuant to the
procedures set forth in Sec. 716.105(b) and (c). EPA finds that there
is ``good cause'' under the Administrative Procedure Act (APA) (5
U.S.C. 553(b)(3)(B)) to make these amendments without prior notice and
comment. EPA believes notice and an opportunity for comment on this
action are unnecessary. TSCA directs the ITC to add chemical substances
to the Priority Testing List for which EPA should give priority
consideration. EPA also lacks the authority to remove a chemical
substance from the Priority Testing List once it has been added by the
ITC. As explained earlier in this preamble, pursuant to Sec.
716.105(b) and (c), once the ITC adds a chemical substance to the
Priority Testing List, EPA adds that chemical substance to the list of
chemical substances subject to the TSCA section 8(d) model rule
reporting requirements, unless the ITC designated and recommended more
than 50 chemical substances or categories of chemical substances in a
calendar year or EPA withdraws the chemical substance from the TSCA
section 8(d) model rule for good cause. EPA promulgated this procedure
in 1985 after having solicited public comment on the need for and
mechanics of this procedure (Ref. 8). Because that rule established the
procedure for adding ITC chemical substances to the TSCA section 8(d)
model rule, it is unnecessary to request comment on the procedure in
this action. Finally, Sec. 716.105(b) and (c) do provide EPA with the
discretion to withdraw a chemical substance from the TSCA section 8(d)
model rule for good cause, including if a party submits to EPA
information showing good cause that a chemical substance should be
removed from the TSCA section 8(d) model rule.
III. Final Rule
A. What chemicals are to be added?
EPA is adding the category of cadmium and cadmium compounds to the
TSCA section 8(d) model rule as requested by the ITC in the 69th ITC
Report (Ref. 9). This final rule requires manufacturers (including
importers) of cadmium or cadmium compounds, including as part of an
article, that have been, or are reasonably likely to be, incorporated
into consumer products to report certain unpublished health and safety
studies to EPA.
B. What are the general reporting requirements and deadlines?
This final rule, issued pursuant to TSCA section 8(d) and its
regulations, requires manufacturers (including importers) of cadmium or
cadmium compounds, including as part of an article, that have been, or
are reasonably likely to be, incorporated into consumer products to
report certain unpublished health and safety studies to EPA. Listed in
this unit are the reporting requirements for the chemical substances
being added by this action to the TSCA section 8(d) model rule.
The following types of persons need to report:
1. Persons who, in the 10 years preceding the date a chemical
substance is listed at Sec. 716.120, either have proposed to
manufacture or import or have manufactured or imported the listed
substance must submit to EPA, during the 60-day reporting period
specified in Sec. 716.65 and according to the reporting schedule set
forth at Sec. 716.60, a copy of each health and safety study which is
in their possession at the time the chemical substance is listed.
2. Persons who, at the time the chemical substance is listed,
propose to manufacture or import, or are manufacturing or importing the
listed chemical substance must submit to EPA during the 60-day
reporting period specified in Sec. 716.65 and according to the
reporting schedule set forth at Sec. 716.60:
i. A copy of each health and safety study which is in their
possession at the time the chemical substance is listed.
ii. A list of the health and safety studies known to them but not
in their possession at the time the chemical substance is listed.
iii. A list of the health and safety studies that are ongoing at
the time the chemical substance is listed and are being conducted by or
for them.
iv. A list of the health and safety studies that are initiated
after the date the chemical substance is listed and will be conducted
by or for them.
v. A list of unpublished studies which have been sent to a Federal
agency with no claims of confidentiality or copies of each such study.
vi. A copy of each health and safety study that was previously
listed as ongoing or subsequently initiated (i.e., listed in accordance
with reporting requirements described at Unit III.B.2.iii. and iv.
respectively) when complete--regardless of completion date.
3. Persons who, after the time the substance is listed, propose to
manufacture or import the listed chemical substance must submit to EPA
during the reporting period specified in Sec. 716.65 and according to
the reporting schedule set forth at Sec. 716.60:
i. A copy of each health and safety study which is in their
possession at the time they propose to manufacture or import the listed
chemical substance.
ii. A list of the health and safety studies known to them but not
in their possession at the time they propose to manufacture or import
the listed chemical substance.
iii. A list of the health and safety studies that are ongoing at
the time they propose to manufacture or import the listed chemical
substance, and are being conducted by or for them.
iv. A list of the health and safety studies that are initiated
after the time they propose to manufacture or import the listed
chemical substance, and will be conducted by or for them.
v. A list of unpublished studies which have been sent to a Federal
agency with no claims of confidentiality or copies of each such study.
vi. A copy of each health and safety study that was previously
listed as ongoing or subsequently initiated (i.e., listed in accordance
with reporting requirements described in Unit III.B.3.iii. and iv.
respectively) when complete--regardless of the completion date.
Generally, the reporting described in Unit III.B. is required by
March 4, 2013. Any person who manufactures or imports, or who proposes
to manufacture or import, the listed chemical substance as described in
Unit III.B. from January 2, 2013 to March 4, 2013 must inform EPA by
submitting a list of any studies initiated during the period from
January 2, 2013 to March 4, 2013 within 30 days of their initiation,
but in no case later than April 2, 2013. In addition, if any such
person has submitted lists of studies that were ongoing or initiated
during the period from January 2, 2013 to March 4, 2013 to EPA, such
person must submit a copy of each study within 30 days after its
completion, regardless of the study's completion date. See Sec. Sec.
716.60 and 716.65.
Detailed requirements for reporting unpublished health and safety
studies are published in 40 CFR part 716. Also found there are
explanations of the reporting exemptions.
C. What are the chemical specific reporting requirements?
Pursuant to Sec. 716.20(b)(5), the types of health, and/or
environmental effects studies that need to be reported and the chemical
substance grade/purity
[[Page 71565]]
requirements that need to be met or exceeded in individual studies for
cadmium and cadmium compounds are as follows:
1. For the category ``cadmium and cadmium compounds'' (defined as
compounds including any unique chemical substance that contains cadmium
as part of that chemical's structure), reporting would extend to all
unpublished health and safety studies generally reportable under
Sec. Sec. 716.10 and 716.20, for example but not limited to those
that:
i. Relate to the cadmium content (either from cadmium or cadmium
compounds) of consumer products (including the specific cadmium
compound (defined in Unit III.A.) used in the products such as surface
coatings and filler), data related to the product formulations, and
function of the cadmium (e.g., stabilizer, colorant, etc.) in the
products.
ii. Relate to the assessment of consumer exposure to cadmium from
such products (including studies of bioavailability, description of the
consumer use (e.g., paints used on plastics), physical form of the
product containing cadmium, method of consumer product application
(e.g., spray applied, etc.), number of potentially exposed consumers).
iii. Include data on cadmium migration from products (e.g.,
conducted using acid extraction or saline solution tests).
iv. Include bio-monitoring data on cadmium presence in tissues.
v. Focus on route, duration, and frequency of exposure to cadmium
in products.
vi. Provide toxicity data on cadmium or cadmium compounds including
in vitro, in vivo, epidemiological, computational, or other studies on
effects of exposure to or use of the cadmium-containing product,
material, or component.
vii. Discuss the function or use of cadmium or cadmium compounds in
a product, material or component including typical concentration.
viii. Include data conducted in compliance with ASTM certification
standards and studies focusing on the effects of the cadmium or cadmium
compounds in consumer products on the health and safety of children.
2. With regard to purity, studies showing any measurable content of
cadmium or cadmium compounds must be submitted.
D. What are the economic implications of this action?
EPA's economic analysis for the addition of cadmium and cadmium
compounds to the Health and Safety Data Reporting rule is entitled
``TSCA Section 8(d): Economic Impact Analysis for the Addition of
Manufacturers and Importers of Consumer Products Containing Cadmium and
Cadmium Compounds From the Sixty-Ninth Report of the TSCA Interagency
Testing Committee to the Health and Safety Data Reporting Rule'' (Ref.
10), and can be found in the docket for this rule.
EPA has estimated that 1,384 firms are subject to the rule and that
28 firms will have relevant studies to submit to EPA. EPA believes
firms that are subject to the rule will need to perform various
activities in order to comply with its requirements. The estimated cost
of this TSCA section 8(d) rule to firms is approximately $481,000.
The estimated cost of this TSCA section 8(d) rule to the Federal
Government is approximately the time of 300 hours. That will amount to
a cost to the Federal Government of approximately $23,500.
IV. Requesting a Chemical Substance Be Withdrawn From the Final Rule
As specified in Sec. 716.105(c), EPA may remove a chemical
substance or category of chemical substances from this final rule for
good cause prior to the effective date of this final rule. Any person
who believes that the reporting required by this final rule is not
warranted for a chemical substance, or the category of chemical
substances listed in this final rule may submit to EPA reasons for that
belief. You must submit your request to EPA on or before December 17,
2012 and in accordance with the instructions provided in Sec.
716.105(c) and (d), which are briefly summarized here. In addition, to
ensure proper receipt by EPA, you should identify docket ID number EPA-
HQ-OPPT-2011-0363 on your request and must submit that request in
accordance with the instructions in Sec. 716.105(c) and (d). If the
Assistant Administrator, Office of Chemical Safety and Pollution
Prevention, withdraws a chemical substance or the category of chemical
substances from this TSCA section 8(d) amendment, in accordance with
Sec. 716.105(c), a Federal Register document announcing this decision
will be published no later than January 2, 2013.
V. References
The docket for this final rule has been established under docket ID
number EPA-HQ-OPPT-2011-0363. The docket is available for review as
specified in ADDRESSES. The following is a listing of the documents
referenced in this preamble that have been placed in the docket for
this final rule:
1. EPA. Requests for Information; Confidentiality of Business
Information; Final Rule. Federal Register (41 FR 36902, September 1,
1976).
2. EPA. Integrated Risk Information System. Cadmium (CASRN 7440-
43-9) IRIS Summary. June 1992. Available online at: https://www.epa.gov/iris/subst/0141.htm.
3. Agency for Toxic Substances and Disease Registry (ATSDR),
U.S. Department of Health and Human Services (HHS). ATSDR
Toxicological Profile for Cadmium (Draft). September 2008. Available
online at: https://www.atsdr.cdc.gov/toxprofiles/tp.asp?id=48&tid=15.
4. Technology Transfer Network Air Toxics Web Site, Cadmium
Compounds (A). January 2000. Available online at: https://epa.gov/ttn/atw/hlthef/cadmium.html.
5. ITC. Sixty-Eighth Report of the TSCA Interagency Testing
Committee to the Administrator of the Environmental Protection
Agency; Receipt of Report and Request for Comments; Notice. Federal
Register (76 FR 46174, August 1, 2011) (FRL-8879-3). Available
online at: https://www.gpo.gov/fdsys/pkg/FR-2011-08-01/pdf/2011-19414.pdf.
6. CPSC. Recalls and Product Safety News. Available online at:
https://www.cpsc.gov/cgi-bin/haz.aspx and select ``Cadmium.''
7. Standard Consumer Safety Specification for Toy Safety, ASTM
F-963. Available online at: https://www.astm.org/Standards/F963.htm
and also available online at: https://www.regulations.gov in docket
ID number EPA-HQ-OPPT-2011-0363.
8. EPA. Chemical Information Rules; Additional Automatic
Reporting; Final Rule. Federal Register (50 FR 34809, August 28,
1985).
9. ITC. Sixty-Ninth Report of the TSCA Interagency Testing
Committee to the Administrator of the Environmental Protection
Agency; Receipt of Report and Request for Comments; Notice. Federal
Register (77 FR 30856, May 23, 2012) (FRL-9346-3). Available online
at: https://www.gpo.gov/fdsys/pkg/FR-2012-05-23/pdf/2012-12493.pdf.
10. EPA. TSCA Section 8(d): Economic Impact Analysis for the
Addition of Manufacturers and Importers of Consumer Products
Containing Cadmium and Cadmium Compounds From the Sixty-Ninth Report
of the TSCA Interagency Testing Committee to the Health and Safety
Data Reporting Rule. May 14, 2012.
VI. Statutory and Executive Order Reviews
A. Regulatory Planning and Review
Under Executive Order 12866 (58 FR 51735, October 4, 1993),
entitled ``Regulatory Planning and Review,'' this action is not a
``significant regulatory action'' and was therefore not reviewed by the
Office of Management and Budget (OMB) under Executive Orders 12866 and
13563, entitled ``Improving
[[Page 71566]]
Regulation and Regulatory Review'' (76 FR 3821, January 21, 2011).
B. Paperwork Reduction Act
The information collection requirements contained in TSCA section
8(d) model rules have already been approved by OMB under the provisions
of the Paperwork Reduction Act (PRA), 44 U.S.C. 3501 et seq., and OMB
control number 2070-0004 (EPA ICR No. 0575). The collection activities
in this final rule are captured by the existing approval and do not
require additional review and/or approval by OMB.
EPA estimates that the information collection activities related to
health and safety data reporting for the category of cadmium and
cadmium compounds in this final rule will result in a total public
reporting burden of 7,019 hours. Of that total, an estimated 2,768
hours are estimated to be spent performing an initial review of the
final rule. The remaining hours are associated with the actual required
reporting activities (Ref. 10). As defined by PRA and 5 CFR 1320.3(b),
``burden'' means the total time, effort, or financial resources
expended by persons to generate, maintain, retain, or disclose or
provide information to or for a Federal agency. This includes the time
needed to: Review instructions; develop, acquire, install, and utilize
technology and systems for the purposes of collecting, validating, and
verifying information, processing and maintaining information, and
disclosing and providing information; adjust the existing ways to
comply with any previously applicable instructions and requirements
which have subsequently changed; train personnel to be able to respond
to a collection of information; search data sources; complete and
review the collection of information; and transmit or otherwise
disclose the information.
Under PRA, an agency may not conduct or sponsor, and a person is
not required to respond to, an information collection request unless it
displays a currently valid OMB control number. The OMB control numbers
for EPA's regulations, including its regulations implementing TSCA
section 8(d) at 40 CFR part 716, are listed in the table in 40 CFR part
9 and included on the related collection instrument. This listing of
the OMB control numbers and their subsequent codification in the CFR
satisfies the display requirements of PRA and OMB's implementing
regulations at 5 CFR part 1320.
C. Regulatory Flexibility Act
This final rule is not subject to the Regulatory Flexibility Act
(RFA), which generally requires an agency to prepare a regulatory
flexibility analysis for any rule that will have a significant economic
impact on a substantial number of small entities. RFA applies only to
rules subject to notice and comment rulemaking requirements under the
Administrative Procedure Act (APA) or any other statute. This rule is
not subject to notice and comment requirements under the APA or any
other statute because although the rule is subject to the APA, the
Agency has invoked the ``good cause'' exemption under 5 U.S.C.
553(b)(3)(B), therefore it is not subject to the notice and comment
requirement.
D. Unfunded Mandates Reform Act
Pursuant to Title II of the Unfunded Mandates Reform Act, 2 U.S.C.
1531-1538, EPA has determined that this final rule does not contain a
Federal mandate that may result in expenditures of $100 million or more
for State, local, and tribal governments, in the aggregate, or the
private sector in any 1 year. In addition, EPA has determined that this
final rule will not significantly or uniquely affect small governments.
Accordingly, the final rule is not subject to the requirements of UMRA
sections 202, 203, 204, or 205.
E. Federalism
Under Executive Order 13132, entitled ``Federalism'' (64 FR 43255,
August 10, 1999), EPA has determined that this final rule does not have
federalism implications because it will not 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, as specified
in the Executive Order. The rule establishes reporting requirements
that apply to manufacturers (including importers) of a category of
cadmium and cadmium compounds. The requirements of this final rule are
not expected to apply to States and localities and would not affect
State and local governments.
F. Indian Tribal Governments
This action will not have tribal implications as specified in
Executive Order 13175, entitled ``Consultation and Coordination With
Indian Tribal Governments'' (65 FR 67249, November 9, 2000). EPA has
determined that this final rule will not have tribal implications
because it will not have substantial direct effects on tribal
governments, 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, as specified in the
Executive Order. EPA has no information to indicate that any tribal
government manufactures or imports the chemical substances covered by
this action.
G. Protection of Children
This action is not subject to Executive Order 13045, entitled
``Protection of Children From Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997), because this action is not an
economically significant regulatory action as defined by Executive
Order 12866. However, cadmium and cadmium compounds are used in toys
that are intended for use by children, and thus presents a
disproportionate risk to children. The agency adequately considered
children's health issues during rule development.
H. Effect on Energy Supply, Distribution, or Use
This action is not a ``significant energy action'' as defined in
Executive Order 13211, entitled ``Actions Concerning Regulations That
Significantly Affect Energy Supply Distribution'' (66 FR 28355, May 22,
2001), because this action is not an economically significant
regulatory action as defined by Executive Order 12866, and it is not
likely to have a significant adverse effect on the supply,
distribution, or use of energy.
I. Technical Standards
Because this action will not involve any technical standards,
section 12(d) of the National Technology Transfer and Advancement Act,
15 U.S.C. 272 note, does not apply to this action.
J. Environmental Justice
This action does not entail special considerations of environmental
justice related issues as delineated by Executive Order 12898, entitled
``Federal Actions To Address Environmental Justice in Minority
Populations and Low-Income Populations'' (59 FR 7629, February 16,
1994). This action is expected to have a positive impact on children in
low-income and minority communities by increasing the amount of cadmium
health and safety data available to EPA and consumers.
VII. Congressional Review Act
Pursuant to the Congressional Review Act, 5 U.S.C. 801 et seq., EPA
will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to
[[Page 71567]]
publication of the rule in the Federal Register. This action is not a
``major rule'' as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 716
Environmental protection, Chemicals, Hazardous substances, Health
and safety studies, Reporting and recordkeeping requirements.
Dated: November 20, 2012.
Wendy C. Hamnett,
Director, Office of Pollution Prevention and Toxics.
Therefore, 40 CFR chapter I is amended as follows:
PART 716--[AMENDED]
0
1. The authority citation for part 716 continues to read as follows:
Authority: 15 U.S.C. 2607(d).
0
2. In Sec. 716.21, add new paragraph (a)(9) to read as follows:
Sec. 716.21 Chemical specific reporting requirements.
(a) * * *
(9) (i) Reporting requirements for the category ``cadmium and
cadmium compounds'' apply only to persons that manufacture (including
import) cadmium or cadmium compounds that have been, or are reasonably
likely to be, incorporated into consumer products.
(A) All unpublished health and safety studies generally reportable
under 40 CFR 716.10 and 716.20 must be reported.
(B) [Reserved]
(ii) With regard to purity, studies showing any measurable content
of cadmium or cadmium compounds in such products must be reported.
(iii) For the purposes of this paragraph (a)(9), consumer product
means any product that is sold or made available to consumers for their
use in or around a permanent or temporary household or residence, in or
around a school, or in or around recreational areas.
* * * * *
3. In Sec. 716.120, add, before the entry ``Chlorinated benzenes,
mono-, di-, tri-, tetra-, and penta-,'' the category ``Cadmium and
cadmium compounds'' and its entry in alphabetical order to the table in
paragraph (c) to read as follows:
Sec. 716.120 Substances and listed mixtures to which this subpart
applies.
* * * * *
(c) * * *
----------------------------------------------------------------------------------------------------------------
CAS No.
Category (examples for Special exemptions Effective date Sunset date
category)
----------------------------------------------------------------------------------------------------------------
* * * * * * *
Cadmium and cadmium compounds ................ .................. January 2, 2013.... March 4, 2013.
(any unique chemical substance
that contains cadmium as part
of that chemical's structure).
Manufacturers (including ................ Sec.
importers). 716.21(a)(9)
* * * * * * *
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* * * * *
[FR Doc. 2012-28840 Filed 11-30-12; 8:45 am]
BILLING CODE 6560-50-P