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GUIDANCE DOCUMENT

Extension of Certain Tobacco Product Compliance Deadlines Related to the Final Deeming Rule Guidance for Industry March 2019

Final
Issued by:
Guidance Issuing Office
Center for Tobacco Products

March 2019

This guidance document is intended to assist any person who manufactures, packages, sells, offers to sell, distributes, or imports for sale and distribution within the United States newly regulated tobacco products, roll-your-own tobacco, and cigarette tobacco.


Submit Comments

Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All comments should be identified with the title of the guidance.

Questions?

Contact Point
Contact CTP
Document Control Center
Center for Tobacco Products
Food and Drug Administration
10903 New Hampshire Ave WO71-G335
Silver Spring, MD 20993-002
AskCTP@fda.hhs.gov
(877) 287-1373 (9am EST-4pm EST)