Extension without change of a currently approved collection
No
Regular
10/23/2023
Requested
Previously Approved
36 Months From Approved
10/31/2023
15,008
15,048
3,527
3,536
0
0
The information collection implements
section 721(a) of the Federal Food Drug, and Cosmetic Act (the act)
(21 U.S.C. 379e(a) providing that a color additive shall be deemed
unsafe unless it meets the requirement of a listing regulation
including any requirement for batch certification. FDA lists color
additives that have been shown to be safe for their intended uses
in Title 21 of the Code of Federal regulations.( CFR). FDA requires
batch certification for all color additives provisionally listed in
21 CFR part 82. Color additives listed in 21 CFR part 73 are
exempted from certification. The requirements for color additive
certification are described in 21 CFR part 80.
Based on a review of the
information collection since our last request for OMB approval, we
have slightly decreased our burden estimate based on our experience
with this program. Although the number of respondents increased,
the number of responses per respondent decreased.
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.