Approved with
the understanding that data collection will not be used to directly
inform FDA enforcement activities or regulatory policy
development.
Inventory as of this Action
Requested
Previously Approved
03/31/2020
36 Months From Approved
1,462
0
0
636
0
0
0
0
0
The Food and Drug Administration would
like to improve its knowledge of the various manufacturing and
quality management practices spanning the cosmetics industry. This
Information Collection Request (ICR) collects information from
cosmetic manufacturers on current manufacturing and quality
management practices to estimate costs associated with achieving
the industry baselines revealed by the survey. This ICR consists of
a one-time survey which aims to provide FDA with information on the
state of the industry.
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.