Today, the Federal Drug Administration (FDA) released their final ruling on cigar regulation. It seems they don’t give a hoot about the pending legislation H.R. 5054: Agriculture, Rural Development, Food and Drug Administration, and Related Agencies Appropriations Act, 2017, eliminating all funding for enforcing FDA cigar regulation. The 499 page document provides regulation for cigars, e-cigarettes, vaping, pipe tobacco, etc. There is a wealth of information in the regulation and over the next couple of weeks, Cigar Intel’s crack intel research analyst, aka c.gar, will go through the regulation and post key information affecting cigar smokers. As far as e-cigarettes, vaping, hookah, etc.. . . we encourage the FDA to have fun regulating these tobaccos types as frankly, we don’t care at all about other types of tobacco.
As a start to our coverage, here is a quote from the FDA announcing their final ruling:
“Extending Authorities to All Tobacco Products, Including E-Cigarettes, Cigars, and Hookah
Tobacco use is the single largest preventable cause of disease and death in the United States. As part of its goal to improve public health and protect future generations from the risks of tobacco use, the FDA has extended its authority to cover all products that meet the definition of a tobacco product. Previously, the FDA regulated cigarettes, cigarette tobacco, roll-your-own tobacco and smokeless tobacco, but in 2016, the FDA finalized a rule – Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act – which extends the FDA’s authority to include the regulation of electronic nicotine delivery systems (such as e-cigarettes and vape pens), all cigars, hookah (water pipe) tobacco, pipe tobacco and nicotine gels, among others. This action is a milestone in consumer protection – going forward, the FDA will be able to:
– Review new tobacco products not yet on the market;
– Help prevent misleading claims by tobacco product manufacturers;
– Evaluate the ingredients of tobacco products and how they are made; and
– Communicate the potential risks of tobacco products.
This final rule goes into effect on August 8, 2016.
Provisions and Requirements
The final rule will subject all manufacturers, importers and/or retailers of newly-regulated tobacco products to any applicable provisions related to tobacco products in the Federal Food, Drug, and Cosmetic Act and FDA regulations, including:
– Registering manufacturing establishments and providing product listings to the FDA;
– Reporting ingredients, and harmful and potentially harmful constituents;
– Requiring premarket review and authorization of new tobacco products by the FDA;
– Placing health warnings on product packages and advertisements; and
– Not selling modified risk tobacco products (including those described as “light,” “low,” or “mild”) unless authorized by the FDA.
In addition, there are several provisions aimed at restricting youth access to tobacco products, including:
– Not allowing products to be sold to persons under the age of 18 years (both in-person and online);
– Requiring age verification by photo ID;
– Not allowing the selling of tobacco products in vending machines (unless in an adult-only facility); and
– Not allowing the distribution of free samples.
Today’s historic rule serves as the foundation for future FDA regulations.”
Historic is right. Wankers.