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Submit Comments on Tobacco Products

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Make your voice heard and be part of our ongoing effort to improve public health in the United States.

We solicit information and comments, announced in the Federal Register and posted in dockets on Regulations.gov, from concerned citizens, industry, and organizations on a wide range of issues related to implementation of the Tobacco Control Act.

Submit Comments

Modified Risk Tobacco Product Application: Application for IQOS 3 System Holder and Charger Submitted by Philip Morris Products S.A.
Docket No: FDA- 2021-N-0408-0001
Date: Currently no deadline for public comments
Summary: The FDA is announcing the availability for public comment of a modified risk tobacco product (MRTP) application for the IQOS 3 System Holder and Charger submitted by Philip Morris Products S.A. FDA will post the application materials on a rolling basis as they are redacted in accordance with applicable laws.

Tobacco Product User Fees: Responses to Frequently Asked Questions
Docket No:
 FDA-2021-D-0373  
Date: July 26, 2021 
Summary: The Food and Drug Administration is announcing the availability of a draft guidance for industry entitled “Tobacco Product User Fees:  Responses to Frequently Asked Questions.”  This draft guidance provides information in response to frequently asked questions related to tobacco product user fees assessed and collected under the Federal Food, Drug, and Cosmetic Act (FD&C Act).


What makes an effective and useful comment?

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.

Your role in shaping tobacco regulation

Our regulatory process generally follows these steps:

  1. Rule/Regulation Proposed
    We publish a proposed rule in the Federal Register.
  2. Public Comments Considered
    Our proposals generally have a 60-90 day review period.
  3. Final Rule Issued
    After considering all comments, we issue a final rule.
  4. Compliance with New Rule Enforced
    We must ensure that retailers and businesses comply with the regulation.

Additional Resources


Audience: Public Health Professionals, Healthcare Providers, Retailers, Manufacturers

Topics: Prevention, Science & Research, Tobacco Product Laws

Source: https://www.fda.gov/tobacco-products/products-guidance-regulations/submit-comments-tobacco-products