I found this response from Missouri State Senetor, Roy Blunt, sitting in my inbox this afternoon.
Perhaps a dim light at the end of the tunnel?
Perhaps a dim light at the end of the tunnel?
Dear Jeffrey:
Thank you for contacting me regarding H.R. 2058, the Food and Drug Administration (FDA) Deeming Authority Clarification Act of 2015.
As you know, the FDA finalized a rule in May 2016 extending their regulatory authority over e-cigarettes, cigars, and other products. The rule would specifically require these newly regulated tobacco product manufacturers to register all products and ingredients with the FDA, market new tobacco products only after FDA review, and provide health warnings on products.
H.R. 2058 would amend the Federal Food, Drug, and Cosmetic Act to require the FDA to make the grandfather date for newly deemed tobacco products begin when the FDA regulation was finalized, as opposed to implementing the regulation from the first effective grandfather date of February 15, 2007.
Currently, H.R. 2058 is pending in the House Energy and Commerce Committee. Should this legislation come before the full Senate for consideration, I will be sure to keep your thoughts and concerns in mind.
Again, thank you for contacting me. I look forward to continuing our conversation on Facebook and Twitter about the important issues facing Missouri and the country. I also encourage you to visit my website to learn more about where I stand on the issues and sign-up for my e-newsletter.
Sincere regards,
Roy Blunt
United States Senator