Per the previous
terms of clearance, "CDC will work with FDAs Center for Tobacco
Products to identify duplication of tobacco product ingredient
collections. No later than one year from the date of this approval,
CDC will submit a brief report to OMB identifying redundancies in
the data collections along with strategies for eliminating
duplication and reducing burden on respondents." The last element
of these terms (strategies for eliminating duplication and reducing
burden on respondents) has not been provided. Therefore, the
collection is being returned as improperly submitted.
Inventory as of this Action
Requested
Previously Approved
09/30/2012
36 Months From Approved
10/01/2012
143
0
143
930
0
930
0
0
0
This is a legislatively mandated
information collection. Since 1986, as required by the
Comprehensive Smoking Education Act of 1984 (CSEA, 15 U.S.C. 1336
or P.L. 98-474) CDC's Office on Smoking and Health has collected
information from cigarette manufacturers, packagers and importers
about the ingredients used in cigarette products. This collection
is commonly known as the Ingredient Report.
US Code:
15
USC 1331 Name of Law: Federal Cigarette Labeling and
Advertising Act
PL:
Pub.L. 98 - 474 1341 Name of Law: Comprehensive Smoking
Education Act
In the previous OMB approval
period, the total burden estimate of 930 hours was based on 143
respondents. The estimates in the current Extension request are
being reduced to 77 respondents and 501 burden hours (a decrease of
66 respondents and 429 burden hours). The decrease in the estimated
number of respondents is based on the actual number of responses
received by OSH for the most recent, complete reporting period
(2010).
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.