Warning Labels and Consumer Understanding

Focus Groups as Used by the Food and Drug Administration

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0497 can be found here:

Documents and Forms

Document Name Document Type
Shay_Warnings Focus Group Screener .doc Other-screener
Shay_Warnings Focus Group Moderator Guide.doc Instruction
Shay_OMB Memorandum Focus Group Study_Warning information.doc justification IC Document
Informed Consent 10_2009.doc Informed consent IC Document

Information Collection (IC) Details

IC Title:	Warning Labels and Consumer Understanding	Agency IC Tracking Number:

IC Status: New

Obligation to Respond: Voluntary

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Other-screener			Shay_Warnings Focus Group Screener .doc		No	No	Paper Only
Instruction			Shay_Warnings Focus Group Moderator Guide.doc		No	No	Paper Only

Line of Business: Health

Subfunction: Public Health Monitoring

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 72	Number of Respondents for Small Entity: 0

Affected Public: Individuals or Households

Percentage of Respondents Reporting Electronically: 0 %

	Approved	Program Change Due to New Statute	Program Change Due to Agency Discretion	Change Due to Adjustment in Agency Estimate	Change Due to Potential Violation of the PRA	Previously Approved
Annual Number of Responses for this IC	72	0	0	0	0	0
Annual IC Time Burden (Hours)	144	0	0	0	0	0
Annual IC Cost Burden (Dollars)	0	0	0	0	0	0

Documents for IC

Title	Document	Date Uploaded
justification	Shay_OMB Memorandum Focus Group Study_Warning information.doc	04/13/2010
Informed consent	Informed Consent 10_2009.doc	04/13/2010

Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.