List of Ingredients Added to Tobacco in the
Manufacture of Cigarette Products
OMB Control No. 0920-0210
Request for Extension
Supporting Statement Part B
Submitted by:
Office on Smoking and Health
National Center of Chronic Disease Prevention
and Health Promotion
Centers for Disease Control and Prevention
Department of Health and Human Services
Project Officer:
Sherrill E. Brady
Policy Team Leader
Telephone: 770-488-5474
Fax: 770-488-5767
E-Mail: Sbrady@cdc.gov
January 16, 2014
Submission of this ICR has been approved by the
HHS/Assistant Secretary for Planning and Evaluation (ASPE)
Table of Contents
Part B. Collections of Information Employing Statistical Methods
B.1 Respondent Universe and Sampling Methods
B.2 Procedures for the Collection of Information
B.3 Methods to Maximize Response Rates and Deal with No Response
B.4 Tests of Procedures or Methods to be Undertaken
B.5 Individuals Consulted on Statistical Aspects and Individuals Collecting and/or Analyzing Data
List of Attachments
Attachment 1a: Comprehensive Smoking Education Act of 1984 (15 U.S.C. ‘ 1335a; Public Law 98-474), relevant portions
Attachment 1b: Federal Cigarette Labeling and Advertising Act (15 U.S.C. ‘ 1331-1341)
Attachment 2: Federal Register Notice (2013)
Attachment 3: Initial Federal Register Notice (1985)
Attachment 4a: Ingredient Report Specifications
Attachment 4b: Reminder Notification Postcard to Manufacturers, Packagers and Importers of Tobacco Products
Attachment 4c: Request for Additional Information from Manufacturers, Packagers and Importers of Tobacco Products
Attachment 5a: HHS/CDC/OSH Web Page on the Comprehensive Smokeless Tobacco Education Act
Attachment 5b: HHS/CDC/OSH Web Page on Tobacco Ingredient Reporting
Attachment 6: Certificate of Compliance for Manufacturers, Packagers and Importers of Tobacco Products
Attachment 7a: Guidelines to Control and Protect Documents that Contain Privileged Information Obtained in Accordance with Sec. 5 (a) of Public Law 98-474
Attachment 7b: Statutory Provisions on Confidentiality (18 U.S.C. ‘ 1905, 5 U.S.C. ‘ 552)
Attachment 8: Federal Register Notice, November 8, 1994, Vol. 59, pp. 55669-55670
Attachment 9: CDC/OSH and FDA Review of Data Collections and Strategies to Reduce Duplicative Collections
Attachment 10a: Public Comment #1, FRN published 10/31/2013
Attachment 10b: CDC Response to Public Comment #1
Attachment 11a: Public Comment #2, FRN published 10/31/2013
Attachment 11b: CDC Response to Public Comment #2
B. COLLECTIONS OF INFORMATION EMPLOYING STATISTICAL METHODS
1. Respondent Universe and Sampling Methods
This data collection does not require the use of statistical methods to select respondents. Responses are required from all cigarette manufacturers, distributors, and importers in the U.S. (referred to collectively as “manufacturers” in this Information Collection Request). OSH reviews and revises the mailing list of cigarette manufactures, packagers, and importers by comparing it to lists available from the tobacco industry, the Federal Trade Commission, and the National Association of Attorneys General, and updates the files as new companies submit ingredient lists.
2. Procedures for the Collection of Information
Each manufacturer, distributor, or importer is required to submit information about the ingredients in each product in its cigarette product line. The information must conform to the specifications established by the Ingredient Report (Attachment 4a), however, manufacturers are not required to submit specific forms. Typically, manufacturers submit a summary report to CDC by mail with the ingredient information for multiple products, often through a designated entity such as legal counsel. The submission must be received on letterhead belonging to the manufacturer or designated representative. Reports may also be submitted via facsimile, but all faxed lists should be followed up with a mailed original. In addition, data may be submitted to CDC by mailing a CD, 3-inch floppy disk, or thumb drive. Electronic mail submissions are not accepted.
The original submission deadline was December 31. In 1994, HHS published an additional Federal Register Notice (November 8, 1994, vol. 59, p. 55669-55670) that changed the due date from December 31 to March 31. A copy of this notice is provided in Attachment 8.
Currently, information for each calendar year is submitted no later than March 31 of the following year. CDC/OSH distributes a postcard reminder (Attachment 4b) to each manufacturer or designated representative in advance of the annual deadline. OSH may follow up by sending a request for additional information (Attachment 4c) if a submission contains incomplete entries or possible errors.
Upon submission and verification of its complete ingredient list, OSH sends a Certificate of Compliance to the manufacturer, distributor, or importer (Attachment 6).
3. Methods to Maximize Response Rates and Deal with No Response
Response is required. Failure to respond will result in legal non-compliance, and inability of manufacturers, packagers, and importers to obtain the Certificate of Compliance required for state-based commercial activity.
4. Tests of Procedures or Methods to be Undertaken
Not applicable. OSH plans to continue the data collection using previously filed information collection methods.
5. Individuals Consulted on Statistical Aspects and Individuals Collecting and/or Analyzing Data
Design of the Information Collection
Allison MacNeil
CDC Office on Smoking and Health
770-488-5529
amacneil@cdc.gov
Information Collection
Ruth L. Hayes (contractor)
CDC Office on Smoking and Health
770-488-5743
rlhayes@cdc.gov
Data Analysis
Paul C. Melstrom
CDC Office on Smoking and Health
770-488-5127
pmelstrom@cdc.gov
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| File Type | application/msword |
| File Title | OMB Supporting Statement |
| Author | sxc7 |
| Last Modified By | CDC User |
| File Modified | 2014-01-16 |
| File Created | 2014-01-16 |