This collection
is approved on the condition that FDA revise the burden statement
to conform to requirements under the Paperwork Reduction Act of
1995.
Inventory as of this Action
Requested
Previously Approved
10/31/2001
10/31/2001
10/31/1998
1
0
50
20
0
20
0
0
0
The registration of cosmetic
manufacturers and repackers supplies FDA with current locations for
on-site inspection, addresses for information and regulatory
mailings, business trading names supplying product distribution
sources, and aids FDA in responding to FOI requests.
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.