Proposed Collection; Comment Request, 36524-36525 [06-5699]
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36524
Federal Register / Vol. 71, No. 123 / Tuesday, June 27, 2006 / Notices
CONSUMER PRODUCT SAFETY
COMMISSION
[Petition HP 06–2]
Petition for Labeling Exemption for
Mini Sparklers
Consumer Product Safety
Commission.
ACTION: Notice.
sroberts on PROD1PC70 with NOTICES
AGENCY:
SUMMARY: The United States Consumer
Product Safety Commission
(Commission or CPSC) has received a
petition (HP 06–2) requesting that the
Commission exempt mini sparkler tubes
from the labeling requirement for
sparklers that states that they must say
‘‘For Outdoor Use Only.’’
DATES: The Office of the Secretary must
receive comments on the petition by
August 28, 2006.
ADDRESSES: Comments on the petition
may be filed by e-mail to cpscos@cpsc.gov. Comments may also be
filed by facsimile to (301) 504–0127, or
delivered or mailed, preferably in five
copies, to the Office of the Secretary,
Consumer Product Safety Commission,
4330 East West Highway, Bethesda, MD
20814, telephone (301) 504–7923.
Comments should be captioned
‘‘Petition HP 06–2, Petition Requesting
Labeling Exemption for Mini
Sparklers.’’ The petition is available on
the CPSC Web site at https://
www.cpsc.gov. A request for a hard copy
of the petition may be directed to the
Office of the Secretary.
FOR FURTHER INFORMATION CONTACT:
Rockelle Hammond, Office of the
Secretary, Consumer Product Safety
Commission, 4330 East West Highway;
telephone (301) 504–6833, e-mail
rhammond@cpsc.gov.
SUPPLEMENTARY INFORMATION: The
Commission has received
correspondence from Octavius Hunt
requesting that the Commission exempt
mini sparkler tubes from the labeling
requirement for sparklers that states that
they must say ‘‘For Outdoor Use Only.’’
The request for the labeling exemption
was docketed as petition number HP
06–2 under the Federal Hazardous
Substances Act, 15 U.S.C. 1261–1278.
Octavius Hunt states that its mini
sparklers are designed and safety-tested
for indoor use according to the British
Standard 7114 Part 2 1988. According to
Octavius Hunt, mini sparklers are
classed as hand-held sparklers under
the British Standard, whereby the total
net explosive content is less than or
equal to 1.5 g per sparkler, which must
burn completely. Octavius Hunt claims
the testing requirements for indoor
hand-held sparklers are more stringent
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17:33 Jun 26, 2006
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than the requirements for outdoor handheld sparklers, and that these stringent
tests mean that these sparklers are
suitable for hand held indoor use.
Octavius Hunt claims the mini sparklers
are designed in order to ensure
composition does not drop off from the
sparkler and that sparks do not emit
from the burning sparkler.
Interested parties may obtain a copy
of the petition on the CPSC Web site at
https://www.cpsc.gov or by writing or
calling the Office of the Secretary,
Consumer Product Safety Commission,
4330 East West Highway, Bethesda, MD
20814; telephone (301) 504–7923.
Dated: June 22, 2006.
Todd A. Stevenson,
Secretary, Consumer Product Safety
Commission.
[FR Doc. E6–10097 Filed 6–26–06; 8:45 am]
BILLING CODE 6355–01–P
DEPARTMENT OF DEFENSE
Department of the Air Force
[No. USAF–2006–0007]
Proposed Collection; Comment
Request
Department of Defense Medical
Examination Review Board.
ACTION: Notice.
AGENCY:
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Department
of Defense Medical Examination Review
Board announces the proposed
extension of a public information
collection and seeks public comment on
the provisions thereof. Comments are
invited on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed information collection; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the information collection on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
DATES: Consideration will be given to all
comments received by August 28, 2006.
ADDRESSES: You may submit comments,
identified by docket number and title,
by any of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
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• Mail: Federal Docket Management
System Office, 1160 Defense Pentagon,
Washington, DC 20301–1160.
Instructions: All submissions received
must include the agency name, docket
number and title for this Federal
Register document. The general policy
for comments and other submissions
from members of the public is to make
these submissions available for public
viewing on the Internet at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
FOR FURTHER INFORMATION CONTACT: To
request more information on this
proposed information collection or to
obtain a copy of the proposal and
associated collection instruments,
please write to: Department of Defense
Medical Examination Review Board
(DoDMERB), 8034 Edgerton Drive, Suite
132, USAF Academy, CO 80840–2200,
Attention: CMSgt Fred Wade.
Title; Associated Form; and OMB
Number: DoDMERB Report of Medical
Examination; DD Forms 2351, 2369,
2370, 2372, 2374, 2378, 2379, 2380,
2381, 2382, 2489, and 2492; OMB
Number 0704–0396.
Needs and Uses: The information
collection requirement is necessary to
determine the medical qualification of
applicants to the five Service academies,
the four-year Reserve Officer Training
Corps College Scholarship Program,
Uniformed Services University of the
Health Sciences, and the Army, Navy,
and Air Force Scholarship and NonScholarship Programs. The collection of
medical history of each applicant is to
determine if applicants meet medical
standards outlined in the Department of
Defense Directive 6130.3, Physical
Standards for Appointment, Enlistment
or Induction.
Affected Public: Individuals or
households.
Annual Burden Hours: 45,000.
Number of Respondents: 45,000.
Responses per Respondent: 1.
Average Burden Per Response: 60
minutes.
Frequency: On occasion.
SUPPLEMENTARY INFORMATION:
Summary of Information Collection
Respondents are individuals who are
interested in applying to attend one of
the five Service academies, the four-year
Reserve Officer Training Corps
Scholarship Program, Uniformed
Services University of the Health
Sciences, or Army, Navy, and Air Force
Scholarship and Non-Scholarship
Programs.
The completed forms are processed
through medical reviewers representing
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Federal Register / Vol. 71, No. 123 / Tuesday, June 27, 2006 / Notices
their respective services to determine a
medical qualification status. Associated
forms may or may not be required
depending on the medical information
contained in the medical examination. If
the medical examination and associated
forms, if necessary, are not
accomplished, individuals reviewing
the medical examination cannot be
readily assured of the medical
qualifications of the individual. Without
this process the individual applying to
any of these programs could not have a
medical qualification determination. It
is essential that individuals have a
medical qualification determination to
ensure compliance with the physical
standards established for each
respective military service program.
Patricia L. Toppings,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 06–5699 Filed 6–26–06; 8:45 am]
[FRL–8189–4]
Public Law-105–270, The Federal
Activities Inventory Reform Act (FAIR)
of 1998; Notice of Public Availability of
EPA Revised 2005 Inventory of
Activities That Are Not Inherently
Governmental and of Activities That
Are Inherently Governmental
Environmental Protection
Agency (EPA).
ACTION: Notice.
sroberts on PROD1PC70 with NOTICES
AGENCY:
SUMMARY: In accordance with the FAIR
Act, agency revised inventories of
activities that are not inherently
governmental are now available to the
public from the Environmental
Protection Agency. The FAIR Act
requires that the agency publish an
announcement of public availability of
the 2005 agency inventories of activities
that are not inherently governmental
when the FAIR Act Challenge Process
results in a change to an agency
inventory.
This is the second release of the 2005
FAIR Act inventories. The EPA has
made the revised 2005 FAIR Act
inventories available for review through
https://www.epa.gov/oarm/inventory/
2005/2005inventory.html.
ADDRESSES: Questions may be directed
to Barbara Stearrett at:
Stearrett.Barbara@epa.gov. U.S.
Environmental Protection Agency,
OARM/Office of Competitive Sourcing
(Mail Code: 3101A), 1200 Pennsylvania
Avenue, NW., Washington, DC 20460.
Jkt 208001
Dated: June 22, 2006.
Susan Kantrowitz,
Team Leader, Information and Human
Resources Team, Office of Policy and
Resources Management.
[FR Doc. E6–10101 Filed 6–26–06; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–8189–3; Docket ID No. EPA–HQ–ORD–
2006–0500]
Draft Toxicological Review of Dibutyl
Phthalate (Di-n-Butyl Phthalate): In
Support of the Summary Information in
the Integrated Risk Information System
(IRIS)
Environmental Protection
Agency (EPA).
ACTION: Notice of peer-review workshop
and public comment period.
ENVIRONMENTAL PROTECTION
AGENCY
17:33 Jun 26, 2006
Barbara Stearrett at (202) 566–1970.
AGENCY:
BILLING CODE 5001–06–M
VerDate Aug<31>2005
FOR FURTHER INFORMATION CONTACT:
SUMMARY: EPA is announcing that the
Oak Ridge Institute of Science and
Education (ORISE), under an
Interagency agreement between the
Department of Energy and EPA, will
convene an independent panel of
experts and organize and conduct an
external peer-review workshop to
review the external review draft
document titled, Toxicological Review
of Dibutyl Phthalate (Di-n-Butyl
Phthalate): In Support of Summary
Information in the Integrated Risk
Information System (IRIS) (NCEA–S–
1755). The EPA also is announcing a
public comment period for the draft
document. EPA will consider comments
and recommendations from the public
and the expert panel meeting when EPA
finalizes the draft document.
The public comment period and the
external peer-review workshop are
separate processes that provide
opportunities for all interested parties to
comment on the document. In addition
to consideration by EPA, all public
comments submitted in accordance with
this notice will also be forwarded to
EPA’s contractor for consideration by
the external peer-review panel prior to
the workshop.
EPA is releasing this draft document
solely for the purpose of predissemination peer review under
applicable information quality
guidelines. This document has not been
formally disseminated by EPA. It does
not represent and should not be
construed to represent any Agency
policy or determination.
ORISE invites the public to register to
attend this workshop as observers. In
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36525
addition, ORISE invites the public to
give brief oral comments at the
workshop regarding the draft document
under review. The draft document and
EPA’s peer-review charge are available
via the Internet on NCEA’s home page
under the Recent Additions and the
Data and Publications menus at https://
www.epa.gov/ncea. When finalizing the
draft document, EPA will consider
ORISE’s report of the comments and
recommendations from the external
peer-review workshop and any public
comments that EPA receives in
accordance with this notice.
DATES: The peer-review panel workshop
will begin on July 28, 2006, at 9 a.m.
and end at 4 p.m. The public comment
period begins June 27, 2006 and ends
July 21, 2006. Technical comments
should be in writing and must be
received by EPA by July 21, 2006.
Comments from the public received by
July 14, 2006, will be submitted to the
panel prior to the workshop.
ADDRESSES: The peer-review workshop
will be held at The American
Geophysical Union, 2000 Florida
Avenue, NW., Washington, DC 20009–
1277. The EPA contractor, ORISE, is
organizing, convening, and conducting
the peer-review workshop. To attend the
workshop, register by July 11, 2006, by
calling ORISE at 865–241–5784, sending
a facsimile to 865–241–3168, or sending
an e-mail to Leslie Shapard,
shapardl@orau.gov. You may also
register via the Internet at https://
www.orau.gov/dibutyl_phthalate. You
must register by July 11, 2006, if you
wish to provide brief oral comments at
the workshop.
The draft Toxicological Review of
Dibutyl Phthalate (Di-n-Butyl
Phthalate): In Support of Summary
Information in the Integrated Risk
Information System (IRIS) is available
via the Internet on the National Center
for Environmental Assessment(s (NCEA)
home page under the Recent Additions
and the Data and Publications menus at
https://www.epa.gov/ncea. A limited
number of paper copies are available
from NCEA(s Technical Information
Staff. Please contact the Technical
Information Staff by telephone at 202–
564–3261 or by facsimile at 202–565–
0050. If you are requesting a paper copy,
please provide your name, mailing
address, and the document title. Copies
are not available from ORISE.
Comments may be submitted
electronically via https://
www.regulations.gov, by mail, by
facsimile, or by hand delivery/courier.
Please follow the detailed instructions
as provided in the SUPPLEMENTARY
INFORMATION section of this notice.
E:\FR\FM\27JNN1.SGM
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Agencies
[Federal Register Volume 71, Number 123 (Tuesday, June 27, 2006)]
[Notices]
[Pages 36524-36525]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-5699]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Department of the Air Force
[No. USAF-2006-0007]
Proposed Collection; Comment Request
AGENCY: Department of Defense Medical Examination Review Board.
ACTION: Notice.
-----------------------------------------------------------------------
In compliance with Section 3506(c)(2)(A) of the Paperwork Reduction
Act of 1995, the Department of Defense Medical Examination Review Board
announces the proposed extension of a public information collection and
seeks public comment on the provisions thereof. Comments are invited
on: (a) Whether the proposed collection of information is necessary for
the proper performance of the functions of the agency, including
whether the information shall have practical utility; (b) the accuracy
of the agency's estimate of the burden of the proposed information
collection; (c) ways to enhance the quality, utility, and clarity of
the information to be collected; and (d) ways to minimize the burden of
the information collection on respondents, including through the use of
automated collection techniques or other forms of information
technology.
DATES: Consideration will be given to all comments received by August
28, 2006.
ADDRESSES: You may submit comments, identified by docket number and
title, by any of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Mail: Federal Docket Management System Office, 1160
Defense Pentagon, Washington, DC 20301-1160.
Instructions: All submissions received must include the agency
name, docket number and title for this Federal Register document. The
general policy for comments and other submissions from members of the
public is to make these submissions available for public viewing on the
Internet at https://www.regulations.gov as they are received without
change, including any personal identifiers or contact information.
FOR FURTHER INFORMATION CONTACT: To request more information on this
proposed information collection or to obtain a copy of the proposal and
associated collection instruments, please write to: Department of
Defense Medical Examination Review Board (DoDMERB), 8034 Edgerton
Drive, Suite 132, USAF Academy, CO 80840-2200, Attention: CMSgt Fred
Wade.
Title; Associated Form; and OMB Number: DoDMERB Report of Medical
Examination; DD Forms 2351, 2369, 2370, 2372, 2374, 2378, 2379, 2380,
2381, 2382, 2489, and 2492; OMB Number 0704-0396.
Needs and Uses: The information collection requirement is necessary
to determine the medical qualification of applicants to the five
Service academies, the four-year Reserve Officer Training Corps College
Scholarship Program, Uniformed Services University of the Health
Sciences, and the Army, Navy, and Air Force Scholarship and Non-
Scholarship Programs. The collection of medical history of each
applicant is to determine if applicants meet medical standards outlined
in the Department of Defense Directive 6130.3, Physical Standards for
Appointment, Enlistment or Induction.
Affected Public: Individuals or households.
Annual Burden Hours: 45,000.
Number of Respondents: 45,000.
Responses per Respondent: 1.
Average Burden Per Response: 60 minutes.
Frequency: On occasion.
SUPPLEMENTARY INFORMATION:
Summary of Information Collection
Respondents are individuals who are interested in applying to
attend one of the five Service academies, the four-year Reserve Officer
Training Corps Scholarship Program, Uniformed Services University of
the Health Sciences, or Army, Navy, and Air Force Scholarship and Non-
Scholarship Programs.
The completed forms are processed through medical reviewers
representing
[[Page 36525]]
their respective services to determine a medical qualification status.
Associated forms may or may not be required depending on the medical
information contained in the medical examination. If the medical
examination and associated forms, if necessary, are not accomplished,
individuals reviewing the medical examination cannot be readily assured
of the medical qualifications of the individual. Without this process
the individual applying to any of these programs could not have a
medical qualification determination. It is essential that individuals
have a medical qualification determination to ensure compliance with
the physical standards established for each respective military service
program.
Patricia L. Toppings,
Alternate OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. 06-5699 Filed 6-26-06; 8:45 am]
BILLING CODE 5001-06-M