Food and Drug Administration, HHS.
The Food and Drug Administration (FDA) is publishing a list of information collections that have been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
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FOR FURTHER INFORMATION CONTACT:
Ila S. Mizrachi, Office of Operations, Food and Drug Administration, Three White Flint North, 10 a.m.-12 p.m., 11601 Landsdown St., North Bethesda, MD 20852, 301-796-7726, PRAStaff@fda.hhs.gov.
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The following is a list of FDA information collections recently approved by OMB under section 3507 of the Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control number and expiration date of OMB approval for each information collection are shown in table 1. Copies of the supporting statements for the information collections are available on the internet at http://www.reginfo.gov/public/do/PRAMain. 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.
Table 1—List of Information Collections Approved By OMB
|Title of collection||OMB control number||Date approval expires|
|FDA Adverse Event and Products Experience Reports; Electronic Submissions||0910-0645||6/30/2022|
|Investigation of Consumer Perceptions of Expressed Modified Risk Claims||0910-0873||6/30/2022|
|Food Labeling: Notification Procedures for Statements on Dietary Supplements||0910-0331||7/31/2022|
|Export Notification and Recordkeeping Requirements||0910-0482||7/31/2022|
|Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act||0910-0641||7/31/2022|
|Sanitary Transportation of Human and Animal Food||0910-0773||7/31/2022|
|Guidance for Industry on Tropical Disease Priority Review Vouchers||0910-0822||7/31/2022|
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Dated: August 1, 2019.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2019-16889 Filed 8-6-19; 8:45 am]
BILLING CODE 4164-01-P