Consumer Product Policy Statement, 63957-63959 [2011-26581]
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Federal Register / Vol. 76, No. 199 / Friday, October 14, 2011 / Notices
date will be considered if it is practical
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received on or before this date.
ADDRESSES: Please include Docket ID
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methods:
specified, as follows:
• Federal rulemaking Web site: Go to
DATE AND TIME: Wednesday October 19,
https://www.regulations.gov and search
2011 at 3 p.m.–4 p.m., EDT.
for documents filed under Docket ID
SUBJECT MATTER: Chairman’s Remarks,
NRC–2010–0292. Address questions
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and Engineering Laboratory and Giant
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• Fax comments to: Secretary, U.S.
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FOR FURTHER INFORMATION CONTACT:
[FR Doc. 2011–26808 Filed 10–12–11; 4:15 pm]
Shirley Xu, Office of Federal and State
BILLING CODE 7555–01–P
Materials and Environmental
Management Programs, U.S. Nuclear
Regulatory Commission, Washington,
NUCLEAR REGULATORY
DC 20555–0001, telephone: 301–415–
COMMISSION
7640; e-mail: Shirley.Xu@nrc.gov.
[NRC–2010–0292]
SUPPLEMENTARY INFORMATION:
NATIONAL SCIENCE FOUNDATION
Consumer Product Policy Statement
Nuclear Regulatory
Commission.
ACTION: Proposed revision to policy
statement; request for public comment.
AGENCY:
The U.S. Nuclear Regulatory
Commission (NRC or Commission) is
proposing to update its policy statement
on products intended for use by the
general public (consumer products).
While the NRC is not making any
significant changes to the policy,
general updating is needed to reflect the
approaches and terminology used in
radiation protection that have evolved
over time, as well as relevant legislation
and regulatory actions.
DATES: Submit comments by December
28, 2011. Comments received after this
tkelley on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
15:20 Oct 13, 2011
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I. Submitting Comments and Accessing
Information
Comments submitted in writing or in
electronic form will be posted on the
NRC Web site and on the Federal
rulemaking Web site, https://
www.regulations.gov. Because your
comments will not be edited to remove
any identifying or contact information,
the NRC cautions you against including
any information in your submission that
you do not want to be publicly
disclosed. The NRC requests that any
party soliciting or aggregating comments
received from other persons for
submission to the NRC inform those
persons that the NRC will not edit their
comments to remove any identifying or
contact information, and therefore, they
should not include any information in
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
63957
their comments that they do not want
publicly disclosed.
You can access publicly available
documents related to this document
using the following methods:
• NRC’s Public Document Room
(PDR): The public may examine and
have copied, for a fee, publicly available
documents at the NRC’s PDR, Room O–
1F21, One White Flint North, 11555
Rockville Pike, Rockville, Maryland.
• NRC’s Agencywide Documents
Access and Management System
(ADAMS):
Publicly available documents created
or received at the NRC are available
online in the NRC Library at https://
www.nrc.gov/reading-rm/adams.html.
From this page, the public can gain
entry into ADAMS, which provides text
and image files of NRC’s public
documents. If you do not have access to
ADAMS or if there are problems in
accessing the documents located in
ADAMS, contact the NRC’s PDR
reference staff at 1–800–397–4209, or
301–415–4737, or by e-mail to
PDR.Resource@nrc.gov.
• Federal Rulemaking Web Site:
Public comments and supporting
materials related to this proposed policy
statement revision can be found at
https://www.regulations.gov by searching
on Docket ID NRC–2010–0292.
II. Background
On March 16, 1965 (30 FR 3462), the
Atomic Energy Commission (AEC), the
NRC’s predecessor agency, issued its
policy statement on products intended
for use by the general public (consumer
products). Under this policy, the AEC
and then the NRC have periodically
reevaluated the overall impact to the
public of products allowed to be
distributed for use by the general public,
which are normally used under an
exemption from licensing of the
consumer-user and from all associated
regulatory requirements. The AEC/NRC
staff has reevaluated the policy at times
and found it to serve the agency well in
spite of the passage of considerable
time. The policy is written in very
general terms and, because of this, has
not needed revision. However, the NRC
is now proposing to update the policy
to include approaches and terminology
more consistent with the evolving
approach to radiation protection, and to
recognize relevant legislative and
regulatory actions.
III. Discussion
The 1965 policy used terms consistent
with the approach to radiation
protection represented primarily in the
early documents of the International
Commission on Radiation Protection
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14OCN1
tkelley on DSK3SPTVN1PROD with NOTICES
63958
Federal Register / Vol. 76, No. 199 / Friday, October 14, 2011 / Notices
(ICRP). These include ‘‘permissible dose
to the gonads’’ and ‘‘permissible body
burden.’’ Newer approaches to radiation
protection do not include such limits.
The recommendations of the ICRP
originally included control of dose to
the gonads because of concern for
potential genetic risks, i.e., risks to
future generations. It has been
determined that genetic risks are much
lower than believed at the time; thus,
separate limits for doses to the gonads
are no longer used. Also, early
approaches to radiation protection
included limits on body burden, i.e., the
amount of a radionuclide present in a
person’s body. In newer approaches for
controlling cumulative exposure from
radionuclides retained in the body, the
calculated dose for the year of intake
includes doses that will result in the
future.
Additional updating is needed due to
legislation that has been enacted since
1965. The Energy Reorganization Act of
1974 revised the Atomic Energy Act in
a number of ways, primarily to separate
the regulatory responsibilities from the
AEC and to create the NRC. Relevant
AEC policies, such as the subject policy,
became NRC policies. Also in 1974, the
Commission was given the authority to
create exemptions from licensing for
special nuclear material in addition to
byproduct material and source material.
The NRC has not issued any exemptions
from licensing for products containing
special nuclear material, but the revised
policy would recognize the authority to
do so.
Another relevant legislative action
was the National Environmental Policy
Act (NEPA) of 1969. In subparagraph
9(c), the policy addresses the
consideration of potential impacts to the
environment from the possible
dispersion of radioactive material and
the uncontrolled disposal of products
used under exemption. This is the
primary environmental impact to be
considered in most instances of
evaluating a potential exemption from
licensing. Specific procedures for
complying with NEPA have been
developed, and are addressed in Title 10
of the Code of Federal Regulations (10
CFR) part 51, ‘‘Environmental
Protection Regulations for Domestic
Licensing and Related Regulatory
Functions.’’ Thus, any rulemaking to
add an exemption from licensing
requirements would require NRC
documentation of environmental
considerations in accordance with these
procedures. In addition, the
responsibilities of the Federal Radiation
Council are now performed within the
Environmental Protection Agency
(EPA).
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15:20 Oct 13, 2011
Jkt 226001
Since the issuance of the 1965 policy,
the NRC has issued class exemptions,
under which additional products
belonging to an identified class of
products can be approved through a
licensing action, if an applicant to
manufacture or distribute a product
demonstrates that the product meets
certain safety criteria. This approach to
exemptions from licensing should also
be recognized in the policy. Also, these
safety criteria include more specific
criteria for accidents than in the existing
policy. The revised policy would better
address the level of risks that are
acceptable for accident and misuse
scenarios. However, the guidance
remains relatively general.
In addition, the example products
noted in paragraphs 5 and 6 of the
policy statement would be revised to be
more relevant and up to date. For
example, thoriated tungsten welding
rods, while available to the public, are
used in unique, expensive equipment
and are not normally used by the public
in the form of consumer products.
Likewise, shipping containers
constructed with uranium as shielding
are not used by the public in the form
of consumer products.
IV. Proposed Revised Statement of
Policy
Products Intended for Use by General
Public (Consumer Products)
Criteria for the approval of products
containing radioactive material and
intended for use by the general public.
This notice sets forth the essential
terms of the Commission’s policy with
respect to approval of the use of
byproduct material, source material, and
special nuclear material in products
intended for use by the general public
(consumer products) without the
imposition of regulatory controls on the
consumer-user. This is accomplished by
the exemption, on a case-by-case basis,
of the possession and use of the
approved items from the licensing
requirements for byproduct, source, or
special nuclear material of the Atomic
Energy Act of 1954, as amended, and of
the Commission’s regulations in 10 CFR
part 30, ‘‘Licensing of Byproduct
Material,’’ 10 CFR part 40, ‘‘Licensing of
Source Material,’’ or 10 CFR part 70,
‘‘Licensing of Special Nuclear Material.’’
1. At the present time it appears
unlikely that the total contribution to
the exposure of the general public to
radiation from the use of radioactivity in
consumer products will exceed a
fraction of limits recommended for
exposure to radiation from all sources.
Information as to total quantities of
radioactive materials being used in such
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Frm 00058
Fmt 4703
Sfmt 4703
products and the number of items being
distributed will be obtained through
recordkeeping and reporting
requirements applicable to the
manufacture and distribution of such
products. Periodically, the NRC staff
conducts an overall reevaluation of this
information to estimate the range of
likely doses to the population. If
radioactive materials are used in
sufficient quantities in products
reaching the public so as to raise any
question of the combined exposure from
multiple consumer products becoming a
significant fraction of the permissible
dose to the public, the Commission will,
at that time, reconsider its policy on the
use of radioactive materials in consumer
products.
2. Approval of a proposed consumer
product, and adding a new exemption
from licensing provision to the
regulations, depends upon both
associated exposures of persons to
radiation and the apparent usefulness of
the product. In general, risks of
exposure to radiation will be considered
to be acceptable if it is shown that in
handling, use, and disposal of the
product, it is unlikely that individuals
in the population will receive more than
a small fraction, less than a few
hundredths, of individual dose limits in
NRC regulations and as recommended
by such groups as the ICRP, the National
Council on Radiation Protection and
Measurements, and the EPA, and that
the probability of individual doses
exceeding any of the specified limits is
low and the probability of individual
doses approaching a level that could
cause immediate effects is negligible.
Otherwise, a decision will be more
difficult and will require a careful
weighing of all factors, including
benefits that will accrue or be denied to
the public as a result of the
Commission’s action. Factors that may
be pertinent are listed in paragraphs 9
and 10, below.
3. Products proposed for distribution
will be useful to some degree. Normally,
the Commission will not attempt an
extensive evaluation of the degree of
benefit or usefulness of a product to the
public. However, in cases where
tangible benefits to the public are
questionable and approval of such a
product may result in widespread use of
radioactive material, such as in common
household items, the degree of
usefulness and benefit that accrues to
the public may be a deciding factor. In
particular, the Commission considers
that the use of radioactive material in
toys, novelties, and adornments may be
of marginal benefit.
4. Applications for approval of ‘‘offthe-shelf’’ items that are subject to
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14OCN1
Federal Register / Vol. 76, No. 199 / Friday, October 14, 2011 / Notices
mishandling, especially by children,
will be approved only if they are found
to combine an unusual degree of utility
and safety.
5. The Commission has approved
certain long-standing uses of source
material, many of which antedate the
atomic energy program. These include:
(a) Use of uranium to color glass for
certain decorative purposes; and
(b) Thorium in various alloys and
products (e.g., gas mantles, optical
lenses, tungsten wire in such things as
electric lamps and vacuum tubes) to
impart desirable physical properties.
6. The Commission also approved the
use of tritium as a substitute luminous
material for the long-standing use of
radium for this purpose on watch and
clock dials and hands.
7. The Commission has approved
additional uses of byproduct and source
material in consumer products. These
include the following:
(a) Tritium and other radionuclides in
electron tubes;
(b) Americium-241 in smoke
detectors; and
(c) Thorium and uranium in
piezoelectric ceramic, which is used in
many electronic products and other
consumer products.
8. In approving uses of byproduct,
source, or special nuclear material in
consumer products, the Commission
establishes limits on quantities or
concentrations of radioactive materials
and, if appropriate, on radiation
emitted. In some cases, other
limitations, such as quality control and
testing, considered important to health
and safety are also specified. In the case
of class exemptions, specific safety
criteria are included in the regulations,
which require the applicant to evaluate
many pathways of exposure of the
public.
tkelley on DSK3SPTVN1PROD with NOTICES
Principal Considerations With Respect
to Evaluation of Products
9. In evaluating proposals for the use
of radioactive materials in consumer
products the principal considerations
are:
(a) The potential external and internal
exposure of individuals in the
population to radiation from the
handling, use and disposal of individual
products;
(b) The potential total cumulative
radiation dose to individuals in the
population who may be exposed to
radiation from a number of products;
(c) The long-term potential external
and internal exposure of the general
population from the uncontrolled
disposal and dispersal into the
environment of radioactive materials
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15:20 Oct 13, 2011
Jkt 226001
from products authorized by the
Commission; and
(d) The benefit that will accrue to or
be denied the public because of the
utility of the product by approval or
disapproval of a specific product.
10. The general criteria for approval of
individual products are set forth in
paragraph 2, above. Detailed evaluation
of potential exposures would take into
consideration the following factors,
together with other considerations,
which may appear pertinent in the
particular case:
(a) The external radiation levels from
the product.
(b) The proximity of the product to
human tissue during use.
(c) The area of tissue exposed. A dose
to the skin of the whole body would be
considered more significant than a
similar dose to a small portion of the
skin of the body.
(d) Potential of the radionuclides to
cause exposures from intakes. Materials
that result in lower cumulative
exposures when taken into the body
would be considered more favorably
than materials that result in higher
exposures from intakes.
(e) The quantity of radioactive
material per individual product. The
smaller the quantity the more favorably
would the product be considered.
(f) Form of material. Materials with a
low solubility in body fluids and the
environment will be considered more
favorably than those with a high
solubility.
(g) Containment of the material.
Products which contain the material
under very severe environmental
conditions will be considered more
favorably than those that will not
contain the material under such
conditions.
(h) Degree of access to product during
normal handling and use. Products
which are inaccessible to children and
other persons during use will be
considered more favorably than those
that are accessible.
Dated at Rockville, Maryland, this 7th day
of October, 2011.
For the Nuclear Regulatory Commission.
Robert J. Lewis,
Acting Deputy Director, Office of Federal and
State Materials and Environmental
Management Programs.
[FR Doc. 2011–26581 Filed 10–13–11; 8:45 am]
BILLING CODE 7590–01–P
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Frm 00059
Fmt 4703
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63959
RAILROAD RETIREMENT BOARD
Proposed Collection; Comment
Request
Summary: In accordance with the
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995
which provides opportunity for public
comment on new or revised data
collections, the Railroad Retirement
Board (RRB) will publish periodic
summaries of proposed data collections.
Comments are invited on: (a) Whether
the proposed information collection is
necessary for the proper performance of
the functions of the agency, including
whether the information has practical
utility; (b) the accuracy of the RRB’s
estimate of the burden of the collection
of the information; (c) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden related to
the collection of information on
respondents, including the use of
automated collection techniques or
other forms of information technology.
1. Title and purpose of information
collection: Appeal Under the Railroad
Retirement and Railroad Unemployment
Insurance Act; OMB 3220–0007.
Under Section 7(b)(3) of the Railroad
Retirement Act (RRA), and Section 5(c)
of the Railroad Unemployment
Insurance Act (RUIA) any person
aggrieved by a decision on his or her
application for an annuity or benefit
under that Act has the right to appeal to
the RRB. This right is prescribed in 20
CFR part 260 and 20 CFR part 320. The
notification letter, which is sent at the
time of the original action on the
application, informs the applicant of
such right. When an applicant protests
a decision, the concerned RRB office
reviews the entire file and any
additional evidence submitted and
sends the applicant a letter explaining
the basis of the determination. The
applicant is then notified that if he or
she wishes to protest further, they can
appeal to the RRB’s Bureau of Hearings
and Appeals. The appeal process is
prescribed in 20 CFR 260.5 and 260.9
and 20 CFR 320.12 and 320.38.
The form prescribed by the RRB for
filing an appeal under the RRA or RUIA
is Form HA–1, Appeal Under the
Railroad Retirement Act or Railroad
Unemployment Insurance Act. The form
asks the applicant to explain the basis
for their request for an appeal and, if
necessary, to describe any additional
evidence they wish to submit in support
of the appeal. Completion is voluntary,
however, if the information is not
provided the RRB cannot process the
appeal. The RRB proposes minor
E:\FR\FM\14OCN1.SGM
14OCN1
Agencies
[Federal Register Volume 76, Number 199 (Friday, October 14, 2011)]
[Notices]
[Pages 63957-63959]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-26581]
=======================================================================
-----------------------------------------------------------------------
NUCLEAR REGULATORY COMMISSION
[NRC-2010-0292]
Consumer Product Policy Statement
AGENCY: Nuclear Regulatory Commission.
ACTION: Proposed revision to policy statement; request for public
comment.
-----------------------------------------------------------------------
SUMMARY: The U.S. Nuclear Regulatory Commission (NRC or Commission) is
proposing to update its policy statement on products intended for use
by the general public (consumer products). While the NRC is not making
any significant changes to the policy, general updating is needed to
reflect the approaches and terminology used in radiation protection
that have evolved over time, as well as relevant legislation and
regulatory actions.
DATES: Submit comments by December 28, 2011. Comments received after
this date will be considered if it is practical to do so, but the NRC
is able to assure consideration only for comments received on or before
this date.
ADDRESSES: Please include Docket ID NRC-2010-0292 in the subject line
of your comments. For instructions on submitting comments and accessing
documents related to this action, see Section I, ``Submitting Comments
and Accessing Information'' in the SUPPLEMENTARY INFORMATION section of
this document. You may submit comments by any one of the following
methods:
Federal rulemaking Web site: Go to https://www.regulations.gov and search for documents filed under Docket ID NRC-
2010-0292. Address questions about NRC dockets to Carol Gallagher,
telephone: 301-492-3668, e-mail: Carol.Gallagher@nrc.gov.
Mail comments to: Secretary, U.S. Nuclear Regulatory
Commission, Washington, DC 20555-0001, Attn: Rulemakings and
Adjudications Staff.
E-mail comments to: Rulemaking.Comments@nrc.gov. If you do
not receive a reply e-mail confirming that we have received your
comments, contact us directly at 301-415-1677.
Hand-deliver comments to: 11555 Rockville Pike, Rockville,
Maryland 20852, between 7:30 a.m. and 4:15 p.m. Federal workdays
(Telephone 301-415-1677).
Fax comments to: Secretary, U.S. Nuclear Regulatory
Commission at 301-415-1101.
FOR FURTHER INFORMATION CONTACT: Shirley Xu, Office of Federal and
State Materials and Environmental Management Programs, U.S. Nuclear
Regulatory Commission, Washington, DC 20555-0001, telephone: 301-415-
7640; e-mail: Shirley.Xu@nrc.gov.
SUPPLEMENTARY INFORMATION:
I. Submitting Comments and Accessing Information
Comments submitted in writing or in electronic form will be posted
on the NRC Web site and on the Federal rulemaking Web site, https://www.regulations.gov. Because your comments will not be edited to remove
any identifying or contact information, the NRC cautions you against
including any information in your submission that you do not want to be
publicly disclosed. The NRC requests that any party soliciting or
aggregating comments received from other persons for submission to the
NRC inform those persons that the NRC will not edit their comments to
remove any identifying or contact information, and therefore, they
should not include any information in their comments that they do not
want publicly disclosed.
You can access publicly available documents related to this
document using the following methods:
NRC's Public Document Room (PDR): The public may examine
and have copied, for a fee, publicly available documents at the NRC's
PDR, Room O-1F21, One White Flint North, 11555 Rockville Pike,
Rockville, Maryland.
NRC's Agencywide Documents Access and Management System
(ADAMS):
Publicly available documents created or received at the NRC are
available online in the NRC Library at https://www.nrc.gov/reading-rm/adams.html. From this page, the public can gain entry into ADAMS, which
provides text and image files of NRC's public documents. If you do not
have access to ADAMS or if there are problems in accessing the
documents located in ADAMS, contact the NRC's PDR reference staff at 1-
800-397-4209, or 301-415-4737, or by e-mail to PDR.Resource@nrc.gov.
Federal Rulemaking Web Site: Public comments and
supporting materials related to this proposed policy statement revision
can be found at https://www.regulations.gov by searching on Docket ID
NRC-2010-0292.
II. Background
On March 16, 1965 (30 FR 3462), the Atomic Energy Commission (AEC),
the NRC's predecessor agency, issued its policy statement on products
intended for use by the general public (consumer products). Under this
policy, the AEC and then the NRC have periodically reevaluated the
overall impact to the public of products allowed to be distributed for
use by the general public, which are normally used under an exemption
from licensing of the consumer-user and from all associated regulatory
requirements. The AEC/NRC staff has reevaluated the policy at times and
found it to serve the agency well in spite of the passage of
considerable time. The policy is written in very general terms and,
because of this, has not needed revision. However, the NRC is now
proposing to update the policy to include approaches and terminology
more consistent with the evolving approach to radiation protection, and
to recognize relevant legislative and regulatory actions.
III. Discussion
The 1965 policy used terms consistent with the approach to
radiation protection represented primarily in the early documents of
the International Commission on Radiation Protection
[[Page 63958]]
(ICRP). These include ``permissible dose to the gonads'' and
``permissible body burden.'' Newer approaches to radiation protection
do not include such limits. The recommendations of the ICRP originally
included control of dose to the gonads because of concern for potential
genetic risks, i.e., risks to future generations. It has been
determined that genetic risks are much lower than believed at the time;
thus, separate limits for doses to the gonads are no longer used. Also,
early approaches to radiation protection included limits on body
burden, i.e., the amount of a radionuclide present in a person's body.
In newer approaches for controlling cumulative exposure from
radionuclides retained in the body, the calculated dose for the year of
intake includes doses that will result in the future.
Additional updating is needed due to legislation that has been
enacted since 1965. The Energy Reorganization Act of 1974 revised the
Atomic Energy Act in a number of ways, primarily to separate the
regulatory responsibilities from the AEC and to create the NRC.
Relevant AEC policies, such as the subject policy, became NRC policies.
Also in 1974, the Commission was given the authority to create
exemptions from licensing for special nuclear material in addition to
byproduct material and source material. The NRC has not issued any
exemptions from licensing for products containing special nuclear
material, but the revised policy would recognize the authority to do
so.
Another relevant legislative action was the National Environmental
Policy Act (NEPA) of 1969. In subparagraph 9(c), the policy addresses
the consideration of potential impacts to the environment from the
possible dispersion of radioactive material and the uncontrolled
disposal of products used under exemption. This is the primary
environmental impact to be considered in most instances of evaluating a
potential exemption from licensing. Specific procedures for complying
with NEPA have been developed, and are addressed in Title 10 of the
Code of Federal Regulations (10 CFR) part 51, ``Environmental
Protection Regulations for Domestic Licensing and Related Regulatory
Functions.'' Thus, any rulemaking to add an exemption from licensing
requirements would require NRC documentation of environmental
considerations in accordance with these procedures. In addition, the
responsibilities of the Federal Radiation Council are now performed
within the Environmental Protection Agency (EPA).
Since the issuance of the 1965 policy, the NRC has issued class
exemptions, under which additional products belonging to an identified
class of products can be approved through a licensing action, if an
applicant to manufacture or distribute a product demonstrates that the
product meets certain safety criteria. This approach to exemptions from
licensing should also be recognized in the policy. Also, these safety
criteria include more specific criteria for accidents than in the
existing policy. The revised policy would better address the level of
risks that are acceptable for accident and misuse scenarios. However,
the guidance remains relatively general.
In addition, the example products noted in paragraphs 5 and 6 of
the policy statement would be revised to be more relevant and up to
date. For example, thoriated tungsten welding rods, while available to
the public, are used in unique, expensive equipment and are not
normally used by the public in the form of consumer products. Likewise,
shipping containers constructed with uranium as shielding are not used
by the public in the form of consumer products.
IV. Proposed Revised Statement of Policy
Products Intended for Use by General Public (Consumer Products)
Criteria for the approval of products containing radioactive
material and intended for use by the general public.
This notice sets forth the essential terms of the Commission's
policy with respect to approval of the use of byproduct material,
source material, and special nuclear material in products intended for
use by the general public (consumer products) without the imposition of
regulatory controls on the consumer-user. This is accomplished by the
exemption, on a case-by-case basis, of the possession and use of the
approved items from the licensing requirements for byproduct, source,
or special nuclear material of the Atomic Energy Act of 1954, as
amended, and of the Commission's regulations in 10 CFR part 30,
``Licensing of Byproduct Material,'' 10 CFR part 40, ``Licensing of
Source Material,'' or 10 CFR part 70, ``Licensing of Special Nuclear
Material.''
1. At the present time it appears unlikely that the total
contribution to the exposure of the general public to radiation from
the use of radioactivity in consumer products will exceed a fraction of
limits recommended for exposure to radiation from all sources.
Information as to total quantities of radioactive materials being used
in such products and the number of items being distributed will be
obtained through recordkeeping and reporting requirements applicable to
the manufacture and distribution of such products. Periodically, the
NRC staff conducts an overall reevaluation of this information to
estimate the range of likely doses to the population. If radioactive
materials are used in sufficient quantities in products reaching the
public so as to raise any question of the combined exposure from
multiple consumer products becoming a significant fraction of the
permissible dose to the public, the Commission will, at that time,
reconsider its policy on the use of radioactive materials in consumer
products.
2. Approval of a proposed consumer product, and adding a new
exemption from licensing provision to the regulations, depends upon
both associated exposures of persons to radiation and the apparent
usefulness of the product. In general, risks of exposure to radiation
will be considered to be acceptable if it is shown that in handling,
use, and disposal of the product, it is unlikely that individuals in
the population will receive more than a small fraction, less than a few
hundredths, of individual dose limits in NRC regulations and as
recommended by such groups as the ICRP, the National Council on
Radiation Protection and Measurements, and the EPA, and that the
probability of individual doses exceeding any of the specified limits
is low and the probability of individual doses approaching a level that
could cause immediate effects is negligible. Otherwise, a decision will
be more difficult and will require a careful weighing of all factors,
including benefits that will accrue or be denied to the public as a
result of the Commission's action. Factors that may be pertinent are
listed in paragraphs 9 and 10, below.
3. Products proposed for distribution will be useful to some
degree. Normally, the Commission will not attempt an extensive
evaluation of the degree of benefit or usefulness of a product to the
public. However, in cases where tangible benefits to the public are
questionable and approval of such a product may result in widespread
use of radioactive material, such as in common household items, the
degree of usefulness and benefit that accrues to the public may be a
deciding factor. In particular, the Commission considers that the use
of radioactive material in toys, novelties, and adornments may be of
marginal benefit.
4. Applications for approval of ``off-the-shelf'' items that are
subject to
[[Page 63959]]
mishandling, especially by children, will be approved only if they are
found to combine an unusual degree of utility and safety.
5. The Commission has approved certain long-standing uses of source
material, many of which antedate the atomic energy program. These
include:
(a) Use of uranium to color glass for certain decorative purposes;
and
(b) Thorium in various alloys and products (e.g., gas mantles,
optical lenses, tungsten wire in such things as electric lamps and
vacuum tubes) to impart desirable physical properties.
6. The Commission also approved the use of tritium as a substitute
luminous material for the long-standing use of radium for this purpose
on watch and clock dials and hands.
7. The Commission has approved additional uses of byproduct and
source material in consumer products. These include the following:
(a) Tritium and other radionuclides in electron tubes;
(b) Americium-241 in smoke detectors; and
(c) Thorium and uranium in piezoelectric ceramic, which is used in
many electronic products and other consumer products.
8. In approving uses of byproduct, source, or special nuclear
material in consumer products, the Commission establishes limits on
quantities or concentrations of radioactive materials and, if
appropriate, on radiation emitted. In some cases, other limitations,
such as quality control and testing, considered important to health and
safety are also specified. In the case of class exemptions, specific
safety criteria are included in the regulations, which require the
applicant to evaluate many pathways of exposure of the public.
Principal Considerations With Respect to Evaluation of Products
9. In evaluating proposals for the use of radioactive materials in
consumer products the principal considerations are:
(a) The potential external and internal exposure of individuals in
the population to radiation from the handling, use and disposal of
individual products;
(b) The potential total cumulative radiation dose to individuals in
the population who may be exposed to radiation from a number of
products;
(c) The long-term potential external and internal exposure of the
general population from the uncontrolled disposal and dispersal into
the environment of radioactive materials from products authorized by
the Commission; and
(d) The benefit that will accrue to or be denied the public because
of the utility of the product by approval or disapproval of a specific
product.
10. The general criteria for approval of individual products are
set forth in paragraph 2, above. Detailed evaluation of potential
exposures would take into consideration the following factors, together
with other considerations, which may appear pertinent in the particular
case:
(a) The external radiation levels from the product.
(b) The proximity of the product to human tissue during use.
(c) The area of tissue exposed. A dose to the skin of the whole
body would be considered more significant than a similar dose to a
small portion of the skin of the body.
(d) Potential of the radionuclides to cause exposures from intakes.
Materials that result in lower cumulative exposures when taken into the
body would be considered more favorably than materials that result in
higher exposures from intakes.
(e) The quantity of radioactive material per individual product.
The smaller the quantity the more favorably would the product be
considered.
(f) Form of material. Materials with a low solubility in body
fluids and the environment will be considered more favorably than those
with a high solubility.
(g) Containment of the material. Products which contain the
material under very severe environmental conditions will be considered
more favorably than those that will not contain the material under such
conditions.
(h) Degree of access to product during normal handling and use.
Products which are inaccessible to children and other persons during
use will be considered more favorably than those that are accessible.
Dated at Rockville, Maryland, this 7th day of October, 2011.
For the Nuclear Regulatory Commission.
Robert J. Lewis,
Acting Deputy Director, Office of Federal and State Materials and
Environmental Management Programs.
[FR Doc. 2011-26581 Filed 10-13-11; 8:45 am]
BILLING CODE 7590-01-P