FDA is reopening the comment for Vape

FDA is reopening the comment for Vape

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Clarification of When Products Made or Derived From Tobacco Are Regulated as Drugs, Devices, or Combination Products; Amendments to Regulations Regarding “Intended Uses”; Reopening of the Comment Period
Docket No.: FDA‐2015‐N‐2002
Dates: Submit comments by December 30, 2015
Summary: The Food and Drug Administration (FDA) is reopening the comment period for the notice of proposed rulemaking (NPRM) that appeared in the Federal Register on September 25, 2015. In the NPRM, FDA requested comments on the proposed regulation that describes the circumstances in which a product made or derived from tobacco that is intended for human consumption will be subject to regulation as a drug, device, or a combination product under the Federal Food, Drug, and Cosmetic Act (the FD&C Act). The Agency is taking this action in response to a request for an extension to allow interested persons additional time to submit comments.

What makes an effective and useful comment?

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Our decisions are based on science and law. We look for logic, good science, and other evidence in the comments we evaluate.

• Provide a clear statement of whether you support or oppose the proposed rule or guidance.
• Include any of the following that support your position:
  • data
  • research
  • analysis
• Read more tips for submitting effective comments on the regulations.gov website.