OMB notes that
this action invloves a substantive change to the collection and
should thus be resubmitted as a revision.
Inventory as of this Action
Requested
Previously Approved
08/31/2010
08/31/2010
12/31/2010
1,042,632
0
1,042,632
1,786,022
0
1,786,022
942,932
0
942,932
Section 403 (21 U.S.C. 343) of the
FFDCA establishes requirements that the label or labeling of a food
product must meet so that it is not misbranded and subject to
regulatory action. Certain of the provisions of section 403 require
that food producers disclose information about themselves or their
products on the labels or labeling of their products. FDA has
issued various regulations in parts 101, 102, 104, and 105 that
also require food producers to disclose certain information on the
labels of their food products. Failure of a food producer to comply
with the provisions of section 403 of the act or of parts 101, 102,
104, or 105 would result in the specific product and the producer
being subject to regulatory action. FDA regulations in parts 101,
102, 104, and 105 require food producers to disclose to consumers
and others specific information about themselves or their products
on the label or labeling of their products. These regulations were
issued under the authority of sections 4, 5, and 6 of the Fair
Packaging and Labeling Act (the FPLA) and of sections 201, 301,
402, 403, 409, and 701 of the FFDCA. Most of the regulations in
Parts 101, 102, 104, and 105 derive from the requirements of
section 403 of the FFDCA, which provides that a food product shall
be misbranded if, among other things, its label or labeling fails
to bear certain required information concerning the food product,
is false or misleading in any particular, or bears certain types of
unauthorized claims. Additionally, FDA has issued regulations among
parts 101, 102, 104, and 105 that require that food producers
retain records relative to the information contained in the label
or labeling of their products and provide those records to
regulatory officials. Finally, certain of the regulations issued by
the agency provide for the submission of petitions to FDA.
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.
Form FDA 3570 Food Labeling Regulations
0381 83-C for form 3570.doc
Food Labeling Regulations