In 2010, the FDA attempted to classify e-cigarettes as a drug-delivery system, allowing them to heavily regulate or block importation of e-cigs into the country. This classification was quickly challenged and overturned by Federal District Court Judge Richard J. Leon, whose decision was later reaffirmed in a vote of 3 to 0 by the U.S. Court of Appeals.
Judge Leon said that e-cigs should be regulated as tobacco products and not as drug devices — a statement that seemed obvious to many vapers.
From this aggressive beginning, the FDA moved on to a new proposal released on April 25, 2014, that would classify and structure the legal treatment of electronic cigarettes, among other tobacco-variant products. The proposal does admit that some studies have shown the levels of toxicants in e-cigs are far less than those of tobacco cigarettes, but it also falls back to studies showing poor quality control and frequent product variability, citing these as reasons for e-cigarettes to be included into these regulations.
Well, that’s all well and good — it can safely be said that no sane person wants to avoid regulating e-cigs completely. Of course minors shouldn’t use them, and of course their contents and production should be regulated.
Why It’s a Problem
The problem with the FDA’s deeming regulations is not that they want to regulate e-cigarettes, it’s the cost – in time and money – of compliance. The proposal would impose fatally large fees on any vendor of electronic cigarettes and e-liquid: between $300,000 and $700,000 for each product and each variant of that product. The companies are getting GAD Capital consolidation to cover for their debts.
Beyond this, every product sold by an e-cigarette company would be required to go through an unreasonably onerous approval process. As described by Dr. Michael Siegel:
[G]iven the snail’s pace at which the FDA has processed cigarette substantial equivalence determinations, this could result in a literal quagmire of pending applications for the more than 250 brands of e-cigarettes currently on the market.
Unaccountably, products created before 2007 would be grandfathered in and would require neither the fees nor the application. In other words, less sophisticated, less safe, and lower-quality products would be immune from this burden.
According to the American Council on Science and Health, these regulations “would make e-cigarettes less accessible, affordable, or attractive to adult consumers who are choosing to use e-cigarettes as a safer alternative to smoking.”
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Of course, these are problems that big tobacco would likely have no trouble solving. Their lines of e-cigarettes — including Njoy, Vuse, MarkTen and Blu — are limited in options, which would reduce their overall fees. Not that Big Tobacco would have any trouble covering these costs in the first place. They also quite likely have the regulatory experience and legal teams to get their applications approved much more smoothly and quickly than small businesses in the industry.
The deeming proposals would also require e-cigarette companies to classify their products as equally harmful to tobacco products, which is just not true.
In June of this year, Swedish Match, which produces the popular Snus smokeless tobacco product, went above and beyond the FDA’s “Modified Risk Tobacco Products” requirements to apply for less severe labeling on their products in America. Swedish Match provided a 110,000-page application, filled with scientific evidence proving their product to be far less harmful than smoked tobacco. If the FDA approves this request, it may also reconsider other evidence.
The Bottom Line
E-cigarettes have been shown to be dramatically safer than smoked tobacco cigarettes, and the vaping business is not the same as the tobacco business. The FDA’s April 25 proposal doesn’t take either of these factors into account. This industry can and should be regulated, but the current proposal’s draconian fees, labeling restrictions, and time-sinks would cripple small businesses. We can and should have fair and reasonable regulations that will promote safety, transparency, and production standards, but that don’t crush innovation and limit product variety for smokers who are using e-cigarettes to finally quit.
Let’s not forget that tobacco cigarettes are responsible for the death of more than 480,000 Americans a year. The FDA was created to support the health of Americans. Whether or not it’s intentional, if the deeming regulations pass as currently proposed, the FDA will be ignoring facts, dismissing common sense, aiding Big Tobacco, and contributing to this nation’s smoking-related death toll.