General identifying information provided by manufacturers and importers of FDA regulated tobacco products and Identification and removal information (monthly); Form FDA 3852

Tobacco Products, User Fees, Requirements for the Submission of Data Needed to Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products

OMB: 0910-0749

IC ID: 207250

Information Collection (IC) Details

View Information Collection (IC)

General identifying information provided by manufacturers and importers of FDA regulated tobacco products and Identification and removal information (monthly); Form FDA 3852
 
No Modified
 
Mandatory
 
21 CFR 1150.5(b)(1) 21 CFR 1150.5(b)(2) 21 CFR 1150.5(a)

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Form and Instruction FDA 3852 Report of Tobacco Product Removals Subject to Tax FDA-3852.pdf Yes Yes Fillable Fileable

Health Public Health Monitoring

 

335 180
   
Private Sector Businesses or other for-profits
 
   90 %

  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 4,020 0 1,620 0 0 2,400
Annual IC Time Burden (Hours) 12,060 0 4,860 0 0 7,200
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Title Document Date Uploaded
Section_1150_5_a_b1_b2_FDA3852 Section_1150_5_a_b1_b2_FDA3852.doc 03/08/2014
            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.

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