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Meeting of the Tobacco Products Scientific Advisory Committee Modified Risk Tobacco Product Applications for ten General brand snus tobacco products / Swedish Match North America, Inc. (PDF)

FDA intends to bring the following matters for discussion with TPSAC: 1. The relative health risks to individual users of the snus tobacco products that are the subject to the proposed modified risk snus tobacco products, particularly with respect to a. g
FDA - Food and Drug Administration
added Apr 14, 2015 15:22


(FDA) recently reviewed your website,, and determined that you sell or distribute e-liquids...FDA has determined that a statement made on the website...regarding your e-liquids violate section 301(tt) of the FD&C Act (21 U.S
FDA - Food and Drug Administration
added Apr 14, 2015 10:55

[Canada] Bill 45, Electronic Cigarettes Act, 2015

The Standing Committee on General Government will meet to consider Bill 45, An Act to enhance public health by enacting the Healthy Menu Choices Act, 2014 and the Electronic Cigarettes Act, 2014 and by amending the Smoke-Free Ontario Act.
Canada Newswire (CNW) (ca)
added Apr 10, 2015 19:08

April 9-10, 2015 – Tobacco Products Scientific Advisory Committee Meeting Announcement

On April 9-10, 2015, the Committee will discuss modified risk tobacco product applications (MRTPAs) submitted by Swedish Match North America Inc. for 10 tobacco products: MR0000020: General Loose, smokeless tobacco, loose snus, 1.59 oz (45g), cardboard c
FDA - Food and Drug Administration
added Apr 9, 2015 16:20

Swedish Paediatric Society LETTER to FDA

emphasizes that the risk with snuff use during pregnancy and in adolescence are considerable, and strongly advise that all young people should avoid using snuff and that all women (also smokers) should refrain from snuff use during pregnancy .
FDA - Food and Drug Administration
added Apr 8, 2015 11:09

Current Intelligence Bulletin 67: Promoting Health and Preventing Disease and Injury Through Workplace Tobacco Policies

National Institute for Occupational Safety and Health (NIOSH)
added Apr 7, 2015 12:54

Demonstrating the Substantial Equivalence of a New Tobacco Product: Responses to Frequently Asked Questions

FDA is finalizing this guidance on many of the topics. In addition, this guidance explains that a manufacturer may submit streamlined SE reports for certain modifications to labels and changes to product quantity.
FDA - Food and Drug Administration
added May 30, 2015 11:16

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

Dates: Extension of comment period- Submit comments by July 2, 2015. Summary: We will hold the third, and final, public workshop to obtain information on electronic cigarettes and the public health on June 1-2, 2015.
FDA - Food and Drug Administration
added Apr 2, 2015 18:52

FTC Releases Reports on 2012 Cigarette and Smokeless Tobacco Sales and Marketing Expenditures

Cigarette Sales Declined, Smokeless Tobacco Sales Increased From 2011 Levels
Federal Trade Commission (FTC)
added Mar 28, 2015 07:20

Smokeless Tobacco Report for 2012 (PDF)

Table 1A shows that the total amount of smokeless tobacco sold by manufacturers to wholesalers and retailers rose from 122.74 million pounds in 2011 to 125.50 million pounds in 2012. Sales revenues received by the manufacturers from wholesalers and ret
Federal Trade Commission (FTC)
added Mar 28, 2015 07:20
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