This collection is approved in accordance with 5 CFR 1320, however, upon resubmission, FDA must provide a written explanation of the steps it has taken to enable electronic reporting of this information and an estimate of when electronic submission will be possible.
Inventory as of this Action
Requested
Previously Approved
03/31/2013
36 Months From Approved
03/31/2010
2,200
0
2,500
1,650
0
1,875
0
0
0
The reporting requirements of this regulation implement the Dietary Supplement Health and Education Act. The subject regulation establishes reporting procedures necessary to inform FDA when dietary supplement manufacturers are making statements of nutritional support on their labels or in their labeling.
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.