Agency Forms Undergoing Paperwork Reduction Act Review, 4723 [2014-01648]
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Federal Register / Vol. 79, No. 19 / Wednesday, January 29, 2014 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–14–0210]
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 (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
(OMB No. 0920–0210, exp. 2/28/2014)—
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
4723
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. Mail Annual Ingredient
Submissions to Attention: FCLAA
Program Manager, Centers for Disease
Control and Prevention, National Center
for Chronic Disease Prevention and
Health Promotion, Office on Smoking
and Health, 4770 Buford Highway, NE.,
MS F–79, Atlanta, GA 30341–3717.
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 annualized
number of respondents is 77 and the
total estimated annualized burden hours
are 501. OMB approval is requested for
three years.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Cigarette Manufacturers, Packagers, and Importers ..............
Ingredient Report ...................
77
1
6.5
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2014–01648 Filed 1–28–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Proposed Project
Centers for Disease Control and
Prevention
tkelley on DSK3SPTVN1PROD with NOTICES
[30Day–14–0338]
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
VerDate Mar<15>2010
16:05 Jan 28, 2014
Jkt 232001
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call (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.
Annual Submission of the Ingredients
Added to, and the Quantity of Nicotine
Contained in, Smokeless Tobacco
Manufactured, Imported, or Packaged in
the U.S. (OMB No. 0920–0338, exp. 2/
28/2014)—Extension—National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
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 the use of
smokeless tobacco products and other
forms of tobacco use through programs
of information, education and research.
Since 1994, as required by the
Comprehensive Smokeless Tobacco
Education Act of 1986 (CSTHEA, 15
U.S.C. 4401 et seq., Pub. L. 99–252),
CDC has collected information about the
ingredients used in smokeless tobacco
products and their nicotine content.
Respondents are commercial smokeless
tobacco product manufacturers,
packagers, or importers (or their
designated representatives), who are
E:\FR\FM\29JAN1.SGM
29JAN1
]]>Agencies
[Federal Register Volume 79, Number 19 (Wednesday, January 29, 2014)]
[Notices]
[Page 4723]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-01648]
[[Page 4723]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-14-0210]
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
(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 (OMB No. 0920-0210, exp. 2/28/2014)--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. Mail Annual Ingredient
Submissions to Attention: FCLAA Program Manager, Centers for Disease
Control and Prevention, National Center for Chronic Disease Prevention
and Health Promotion, Office on Smoking and Health, 4770 Buford
Highway, NE., MS F-79, Atlanta, GA 30341-3717.
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
annualized number of respondents is 77 and the total estimated
annualized burden hours are 501. OMB approval is requested for three
years.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Cigarette Manufacturers, Packagers, Ingredient Report...... 77 1 6.5
and Importers.
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2014-01648 Filed 1-28-14; 8:45 am]
BILLING CODE 4163-18-P
