Guidance for Industry on Labeling for Products Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Act: Questions and Answers

Guidance for Industry on Labeling for Products Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Act: Questions and Answers

OMB: 0910-0641

IC ID: 188840

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Document Name
Document Type
Other-Guidance
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Guidance for Industry on Labeling for Products Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Act: Questions and Answers
 
No Modified
 
Voluntary
 
21 CFR 379aa  (To search for a specific CFR, visit the Code of Federal Regulations.)

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Other-Guidance Guidance OTCADRqa 1-25-13.pdf Yes No Paper Only

Health Public Health Monitoring

 

200 0
   
Individuals or Households
 
   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 100,000 0 0 0 100,000 0
Annual IC Time Burden (Hours) 400,000 0 0 0 400,000 0
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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