Proposed Data Collection Submitted for Public Comment and Recommendations
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Abstract
The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a continuing information collection project titled List of Ingredients Added to Tobacco in the Manufacture of Cigarette Products. The proposed collection allows CDC's Office of Smoking and Health (OSH) to collect information about the ingredients used in cigarette products, a responsibility that has been delegated to CDC by HHS.
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<title>Federal Register, Volume 86 Issue 184 (Monday, September 27, 2021)</title>
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[Federal Register Volume 86, Number 184 (Monday, September 27, 2021)]
[Notices]
[Pages 53308-53309]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2021-20844]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-21-0210; Docket No. CDC-2021-0102]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
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SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a continuing
information collection project titled List of Ingredients Added to
Tobacco in the Manufacture of Cigarette Products. The proposed
collection allows CDC's Office of Smoking and Health (OSH) to collect
information about the ingredients used in cigarette products, a
responsibility that has been delegated to CDC by HHS.
DATES: CDC must receive written comments on or before November 26,
2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0102 by any of the following methods:
<bullet> Federal eRulemaking Portal: <a href="http://Regulations.gov">Regulations.gov</a>. Follow the
instructions for submitting comments.
<bullet> Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS-H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to <a href="http://Regulations.gov">Regulations.gov</a>.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed
above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS H21-8, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
<a href="/cdn-cgi/l/email-protection#fb949699bb989f98d59c948d"><span class="__cf_email__" data-cfemail="0966646b496a6d6a276e667f">[email protected]</span></a>.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses; and
5. Assess information collection costs.
Proposed Project
List of Ingredients Added to Tobacco in the Manufacture of
Cigarette Products (OMB Control No. 0920-0210, Exp. 4/30/2022)--
Extension--National Center for Chronic Disease Prevention and Health
Promotion (NCCDPHP),
[[Page 53309]]
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Cigarette smoking is the leading preventable cause of premature
death and disability in our nation. Each year more than 480,000 deaths
occur as the result of cigarette smoking-related diseases. The CDC's
Office on Smoking and Health (OSH) is the lead federal agency for
comprehensive tobacco prevention and control. Since 1986, as required
by the Comprehensive Smoking Education Act (CSEA) of 1984, which
amended the Federal Cigarette Labeling and Advertising Act (FCLAA), 15
U.S.C. 1335a, CDC has collected information about the ingredients used
in cigarette products. HHS has delegated responsibility for
implementing the required information collection to CDC's OSH.
Respondents are commercial cigarette manufacturers, packagers, or
importers (or their representatives), who are required by FCLAA 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. The information collected is subject to strict
confidentiality provisions.
Ingredient reports are due annually on March 31. Information is
submitted to CDC by mailing or faxing a written report on the
respondent's letterhead. All faxed lists should be followed up with a
mailed original. Electronic mail submissions are not accepted. Mail
Annual Ingredient Submissions to Attention: FCLAA Program Manager,
Office on Smoking and Health, National Center for Chronic Disease
Prevention and Health Promotion, Centers for Disease Control and
Prevention, 4770 Buford Highway NE, MS S107-7, Atlanta, GA 30341-3717.
Upon receipt and verification of the annual ingredient report, CDC
issues a Certificate of Compliance to the respondent. As deemed
appropriate by the Secretary of HHS, HHS is authorized to use the
information to report to Congress the health effects of ingredients,
research activities related to the health effects of ingredients, and
other information that the Secretary determines to be of public
interest.
There are no costs to respondents other than their time. The total
estimated annualized burden hours are 358. OMB approval is requested
for three years.
Estimated Annualized Burden Hours
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Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
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Business Entities............. N/A............. 55 1 6.5 358
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Total..................... ................ .............. .............. .............. 358
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Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-20844 Filed 9-24-21; 8:45 am]
BILLING CODE 4163-18-P
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