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  1. Rules, Regulations and Guidance

FDA's Deeming Regulations for E-Cigarettes, Cigars, and All Other Tobacco Products

Tobacco use is the single largest preventable cause of disease and death in the United States.1 Since 2009, FDA has regulated cigarettes, smokeless, and roll-your-own tobacco. FDA finalized a rule, effective August 8, 2016, to regulate all tobacco products. 

How Do the Regulations Affect You?

Manufacturer?

Do you ...

  • mix e-liquids?
  • make or modify any type of vaping device?
  • mix loose tobacco for people to smoke in a pipe?
  • roll or blend tobacco for cigars?
  • manufacture loose tobacco for consumers to roll their own cigarettes?
  • import tobacco products?
  • manufacture any tobacco product?

If you answered yes to any of these questions, you may be a manufacturer.

Retailer?

Do you ...

  • sell cigars?
  • sell hookah tobacco?
  • sell e-cigarettes or e-liquids?
  • sell any tobacco product?

If you answered yes to any of these questions, you are a retailer.

If you mix e-liquids, make or modify vaporizers, or mix loose tobacco, and you also sell these products, you may be regulated as both a retailer and a manufacturer.


What if I am both a manufacturer and a retailer?


Questions & Answers

  1. What are the costs associated with submitting an application?
  2. I am a vape shop with hundreds of different e-liquids. Do I need to submit an application for each flavor/ingredient variant or nicotine strength?
  3. How does a manufacturer know if they need to conduct clinical trials?
  4. What is the grandfather date?
  5. Are there any e-cigarettes that are grandfathered and could be used as a predicate for a Substantial Equivalence application?

Read more commonly asked questions and answers.


Webinars


Watch additional compliance webinars.


Documents and Additional Resources

Final Rule and Accompanying Documents


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