[Federal Register Volume 84, Number 152 (Wednesday, August 7, 2019)]
[Notices]
[Pages 38633-38634]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-16889]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2018-N-4131, FDA-2018-N-0821, FDA-2013-N-0032, FDA-
2014-N-0801, FDA-2007-D-0429, FDA-2013-N-0013, and FDA-2008-D-0530]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: 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.
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,
[email protected].
SUPPLEMENTARY INFORMATION: 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
------------------------------------------------------------------------
OMB control Date approval
Title of collection number expires
------------------------------------------------------------------------
FDA Adverse Event and Products 0910-0645 6/30/2022
Experience Reports; Electronic
Submissions............................
Investigation of Consumer Perceptions of 0910-0873 6/30/2022
Expressed Modified Risk Claims.........
Food Labeling: Notification Procedures 0910-0331 7/31/2022
for Statements on Dietary Supplements..
Export Notification and Recordkeeping 0910-0482 7/31/2022
Requirements...........................
Labeling of Nonprescription Human Drug 0910-0641 7/31/2022
Products Marketed Without an Approved
Application as Required by the Dietary
Supplement and Nonprescription Drug
Consumer Protection Act................
Sanitary Transportation of Human and 0910-0773 7/31/2022
Animal Food............................
Guidance for Industry on Tropical 0910-0822 7/31/2022
Disease Priority Review Vouchers.......
------------------------------------------------------------------------
[[Page 38634]]
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