FDA and Juul E-Cig Regs Should Keep Anti-Smoking Zealots at Bay

  • RealClearHealth | by: Peter J. Pitts and Robert M. Goldberg |
  • 11/16/2018 12:00 AM
This week FDA Commissioner Scott Gottlieb announced a plan to close the on-ramp to kids using e-cigarettes while preserving adult use of “potentially less harmful forms of nicotine delivery.” The plan's centerpiece curbs the sale of flavored e-cigarettes, which regulators claim entice youth (logic that apparently doesn't extend to Absolut Peach vodka or Jack Daniel's cinnamon whiskey), but which also help smokers quit because they don't remind them of traditional cigarettes.
 
The problem is that anti-smoking zealots want to go further and remove e-cigarettes from the market altogether while leaving most tobacco products untouched. That would snuff out the most impactful public health development in decades. The FDA’s action is designed to reduce e-cigarette use among high school and middle school students “because there is also evidence that a large percentage of these children will become addicted to nicotine and ultimately take up smoking." Yet plummeting and all-time low smoking rates – especially among young adults – would suggest otherwise. In contrast, the FDA recognizes that use of e-cigarettes can help adults stop smoking.
 
Days before the FDA's announcement, e-cigarette manufacturer Juul, which commands about 75 percent of the e-cigarette market share, self-imposed regulations to curb teen use of its products. Juul's "Youth Prevention Plan" will eliminate pod flavors, such as cucumber and mango, from the 90,000 or so retail outlets across the country.
 
Sign Up for Our Email Newsletter

RECENT NEWS

The coronavirus could help pharma reset its reputation in Washington

The coronavirus could help pharma reset its reputation in Washington

The coronavirus outbreak could be the pharmaceutical industry’s ticket to saving its reputation in Washington....  Read more

The biggest challenge facing the FDA’s new Rare Disease Innovation Hub

The biggest challenge facing the FDA’s new Rare Disease Innovation Hub

Differing philosophies within and outside of government could doom the hub...  Read more

Tort bar’s newest collateral damage: Preterm babies

Tort bar’s newest collateral damage: Preterm babies

Lawsuits allege links between intestinal disease, infant formula and human milk fortifiers...  Read more

DRUGWONKS BLOG