Agency Forms Undergoing Paperwork Reduction Act Review, 37677-37678 [2012-15354]
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37677
Federal Register / Vol. 77, No. 121 / Friday, June 22, 2012 / Notices
All of the current McCaffrey’s
supermarkets are located outside the
relevant geographic area. Its Yardley,
Pennsylvania, store is approximately six
miles, and approximately 15 minutes
driving time, from the Genuardi’s in
Newtown. The Newtown Genuardi’s is
outside McCaffrey’s primary service
area and vice versa.
The proposed Order requires
Respondents Ahold and Safeway to
divest the assets of the Genuardi’s to
McCaffrey’s no later than ten days
following Ahold’s acquisition of the 16
Genuardi’s stores that are subject to the
Asset Purchase Agreement. If
McCaffrey’s ultimately is not approved
by the Commission to purchase the
assets, Respondents must immediately
rescind the divestiture and divest the
Newtown Genuardi’s assets to a buyer
that receives the Commission’s prior
approval. The proposed Order contains
additional provisions designed to
ensure the adequacy of the proposed
relief. For example, for a period of one
year, the Order prohibits Respondents
from interfering with the hiring of or
employment of any employees currently
working at the Newtown Genuardi’s.
Additionally, for a period of ten years,
Ahold is required to give the
Commission prior notice of plans to
acquire a supermarket, or an interest in
a supermarket, that has operated or is
operating in Newtown, Pennsylvania.
interpretation of the proposed Consent
Agreement, nor does it modify its terms
in any way.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2012–15308 Filed 6–21–12; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–12–0210]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
V. Opportunity for Public Comment
Proposed Project
The proposed Consent Agreement has
been placed on the public record for 30
days to solicit comments from interested
persons. Comments received during this
period will become part of the public
record. After 30 days, the Commission
will again review the proposed Consent
Agreement, as well as the comments
received, and will decide whether to
modify the proposed Consent
Agreement, withdraw its acceptance of
the proposed Consent Agreement, or
issue its final Consent Orders.
The sole purpose of this Analysis is
to facilitate public comment on the
proposed Consent Agreement. This
Analysis does not constitute an official
List of Ingredients Added to Tobacco
in the Manufacture of Cigarette
Products—Extension—Office on
Smoking and Health, National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), Office on Smoking
and Health (OSH) has the primary
responsibility for the Department of
Health and Human Services (HHS)
smoking and health program. HHS’s
overall goal is to reduce death and
disability resulting from cigarette
smoking and other forms of tobacco use
through programs of information,
education and research.
Since 1986, as required by the
Comprehensive Smoking Education Act
of 1984 (CSEA, 15 U.S.C. 1336 or
Pub. L. 98–474), CDC has collected
information about the ingredients used
in cigarette products. Respondents are
commercial cigarette manufacturers,
packagers, or importers (or their
representatives), who are required by
the CSEA to submit ingredient reports to
HHS on an annual basis.
Respondents are not required to
submit specific forms, however, they are
required to submit a list of all
ingredients used in their products. CDC
requires the ingredient report to be
submitted by chemical name and
Chemical Abstract Service (CAS)
Registration Number, consistent with
accepted reporting practices for other
companies currently required to report
ingredients added to other consumer
products. Typically, respondents submit
a summary report to CDC with the
ingredient information for multiple
products, or a statement that there are
no changes to their previously
submitted ingredient report.
Ingredient reports for new products
are due at the time of first importation.
Thereafter, ingredient reports are due
annually on March 31. Information is
submitted to OSH by mailing a written
report on the respondent’s letterhead, by
CD, three-inch floppy disk, or thumb
drive. Electronic mail submissions are
not accepted. The estimated burden per
response is 6.5 hours.
Upon receipt and verification of the
annual ingredient report, OSH issues a
Certificate of Compliance to the
respondent. OSH also uses the
information to report to the Congress (as
deemed appropriate) discussing the
health effects of these ingredients.
There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
501.
wreier-aviles on DSK7SPTVN1PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Cigarette Manufacturers, Packagers, and Importers ..................................................................
77
1
6.5
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37678
Federal Register / Vol. 77, No. 121 / Friday, June 22, 2012 / Notices
Dated: June 15, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI),
Office of the Associate Director for Science
(OADS), Office of the Director, Centers for
Disease Control and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3262–PN]
[FR Doc. 2012–15354 Filed 6–21–12; 8:45 am]
Medicare and Medicaid Programs;
Application From American
Association for Accreditation of
Ambulatory Surgery Facilities for
Continued Approval of Its Ambulatory
Surgery Facilities Accreditation
Program
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Medicare and
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
Board of Scientific Counselors,
National Center for Environmental
Health/Agency for Toxic Substances
and Disease Registry: Notice of
Charter Renewal
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the Board
of Scientific Counselors, National
Center for Environmental Health/
Agency for Toxic Substances and
Disease Registry, Department of Health
and Human Services, has been renewed
for a 2-year period through May 21,
2014.
For information, contact Vikas Kapil,
Designated Federal Officer, Board of
Scientific Counselors, National Center
for Environmental Health/Agency for
Toxic Substances and Disease Registry,
Department of Health and Human
Services, 4770 Buford Highway
Mailstop F61, Chamblee, Georgia 30341,
telephone 770/488–8316 or fax 770/
488–3385.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: June 13, 2012.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
wreier-aviles on DSK7SPTVN1PROD with NOTICES
[FR Doc. 2012–14923 Filed 6–21–12; 8:45 am]
BILLING CODE 4163–18–P
VerDate Mar<15>2010
15:20 Jun 21, 2012
Jkt 226001
This proposed notice with
comment period acknowledges the
receipt of an application from the
American Association for Accreditation
of Ambulatory Surgery Facilities
(AAAASF) for continued recognition as
a national accrediting organization for
ambulatory surgery centers (ASCs) wish
to participate in the Medicare or
Medicaid programs.
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on July 23, 2012.
ADDRESSES: In commenting, please refer
to file code CMS–3262–PN. Because of
staff and resource limitations, we cannot
accept comments by facsimile (Fax)
transmission.
You may submit comments in one of
four ways (please choose only one of the
ways listed):
1. Electronically. You may submit
electronic comments on this regulation
to https://www.regulations.gov. Follow
the ‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–3262–PN, P.O. Box 8010,
Baltimore, MD 21244–8010.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY: Centers for
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–3262–PN,
Mail Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
4. By hand or courier. If you prefer,
you may deliver (by hand or courier)
your written comments before the close
of the comment period to either of the
following addresses:
SUMMARY:
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a. For delivery in Washington, DC—
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Room 445–G, Hubert
H. Humphrey Building, 200
Independence Avenue SW.,
Washington, DC 20201.
(Because access to the interior of the
Hubert H. Humphrey Building is not
readily available to persons without
Federal government identification,
commenters are encouraged to leave
their comments in the CMS drop slots
located in the main lobby of the
building. A stamp-in clock is available
for persons wishing to retain a proof of
filing by stamping in and retaining an
extra copy of the comments being filed.)
b. For delivery in Baltimore, MD—
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
If you intend to deliver your
comments to the Baltimore address,
please call telephone number (410) 786–
7195 in advance to schedule your
arrival with one of our staff members.
Comments mailed to the addresses
indicated as appropriate for hand or
courier delivery may be delayed and
received after the comment period.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Georganne Kuberski, (410) 786–0799.
Patricia Chmielewski, (410) 786–6899.
Cindy Melanson, (410) 786–0310.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following Web
site as soon as possible after they have
been received: https://
www.regulations.gov. Follow the search
instructions on that Web site to view
public comments.
Comments received timely will also
be available for public inspection as
they are received, generally beginning
approximately 3 weeks after publication
of a document, at the headquarters of
the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
E:\FR\FM\22JNN1.SGM
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]]>Agencies
[Federal Register Volume 77, Number 121 (Friday, June 22, 2012)]
[Notices]
[Pages 37677-37678]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-15354]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30-Day-12-0210]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-7570 or send an email to
omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
List of Ingredients Added to Tobacco in the Manufacture of
Cigarette Products--Extension--Office on Smoking and Health, National
Center for Chronic Disease Prevention and Health Promotion (NCCDPHP),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC), Office on
Smoking and Health (OSH) has the primary responsibility for the
Department of Health and Human Services (HHS) smoking and health
program. HHS's overall goal is to reduce death and disability resulting
from cigarette smoking and other forms of tobacco use through programs
of information, education and research.
Since 1986, as required by the Comprehensive Smoking Education Act
of 1984 (CSEA, 15 U.S.C. 1336 or Pub. L. 98-474), CDC has collected
information about the ingredients used in cigarette products.
Respondents are commercial cigarette manufacturers, packagers, or
importers (or their representatives), who are required by the CSEA to
submit ingredient reports to HHS on an annual basis.
Respondents are not required to submit specific forms, however,
they are required to submit a list of all ingredients used in their
products. CDC requires the ingredient report to be submitted by
chemical name and Chemical Abstract Service (CAS) Registration Number,
consistent with accepted reporting practices for other companies
currently required to report ingredients added to other consumer
products. Typically, respondents submit a summary report to CDC with
the ingredient information for multiple products, or a statement that
there are no changes to their previously submitted ingredient report.
Ingredient reports for new products are due at the time of first
importation. Thereafter, ingredient reports are due annually on March
31. Information is submitted to OSH by mailing a written report on the
respondent's letterhead, by CD, three-inch floppy disk, or thumb drive.
Electronic mail submissions are not accepted. The estimated burden per
response is 6.5 hours.
Upon receipt and verification of the annual ingredient report, OSH
issues a Certificate of Compliance to the respondent. OSH also uses the
information to report to the Congress (as deemed appropriate)
discussing the health effects of these ingredients.
There are no costs to respondents other than their time. The total
estimated annualized burden hours are 501.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Cigarette Manufacturers, Packagers, and Importers............ 77 1 6.5
----------------------------------------------------------------------------------------------------------------
[[Page 37678]]
Dated: June 15, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI), Office of the Associate
Director for Science (OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2012-15354 Filed 6-21-12; 8:45 am]
BILLING CODE 4163-18-P
