2011-2662. Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and ...
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AGENCY:
Food and Drug Administration, HHS.
ACTION:
Notice.
SUMMARY:
The Food and Drug Administration (FDA) is announcing that a collection of information entitled “Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Questions and Answers” has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Elizabeth Berbakos, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50-400B, Rockville, MD 20850, 301-796-3792, Elizabeth.Berbakos@fda.hhs.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
In the Federal Register of February 24, 2009 (74 FR 8264), the Agency announced that the proposed information collection had been submitted to OMB for review and clearance under 44 U.S.C. 3507. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910-0640. The approval expires on July 31, 2012. A copy of the supporting statement for this information collection is available on the Internet at http://www.reginfo.gov/public/do/PRAMain.
Start SignatureDated: February 1, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2011-2662 Filed 2-7-11; 8:45 am]
BILLING CODE 4160-01-P
Document Information
- Published:
- 02/08/2011
- Department:
- Food and Drug Administration
- Entry Type:
- Notice
- Action:
- Notice.
- Document Number:
- 2011-2662
- Pages:
- 6798-6798 (1 pages)
- Docket Numbers:
- Docket No. 2007-D-0429, Formerly Docket No. 2007D-0496
- PDF File:
- 2011-2662.pdf
- Supporting Documents:
- » Guidance for Industry - Question and Answers regarding the labeling of nonprescription human drug products marketed without an approved application as reqired by the dietary supplement and nonprescription drug consumer protection act: revision 1
- » NO DOCUMENT POSTED - See FDA-2007-D-0429-0004
- » NO DOCUMENT POSTED - See FDA-2007-D-0429-0003