JUUL Slapped with FDA Warning Letter for Health Claims

JUUL Labs, an e-cigarette products company that is 35% owned by Altria (NYSE: MO) and an expected partner of Cronos Group (TSX: CRON)(NASDAQ: CRON), was slapped with an FDA warning letter this morning as a result of its advertising and marketing practices which contain unsubstantiated claims related to the health benefits of vaping using JUUL products over that of smoking traditional cigarettes.

Specifically, the claims were found as a result of a hearing at a House Subcommittee focused on “Examining JUUL’s Role in the Youth Nicotine Epidemic.” In particular, it found that numerous claims were told to youth by JUUL sales representatives during sales pitches and presentations including,

  • A JUUL representative speaking with students at his presentation stated that JUUL “was much safer than cigarettes” and that “FDA would approve it any day.”
  • The JUUL representative speaking with students at his presentation called JUUL “totally safe.”
  • The JUUL representative speaking with students at his presentation stated that a student “…should mention JUUL to his [nicotine-addicted] friend…because that’s a safer alternative than smoking cigarettes, and it would be better for the kid to use.
  • The JUUL representative speaking with students at his presentation stated, “FDA was about to come out and say it [JUUL] was 99% safer than cigarettes…and that…would happen very soon….”

In addition, the FDA cited that JUUL was in violation of a number of marketing related misrepresentations of its products.

Antimony Resources — sponsored Sponsored · Antimony Resources

“…your firm has engaged in labeling, advertising, and/or other activities directed to consumers, in which JUUL explicitly and/or implicitly has represented that JUUL products are free of a substance, have a reduced level of or exposure to a substance, and/or that JUUL products present a lower risk of tobacco-related disease or are less harmful than one or more other commercially marketed tobacco products.”

Certain of the presentations were found to have been conducted directly in schools, wherein JUUL stated that using its products were “99% safer than cigarettes.”

The FDA finalized its letter by stating that an exhaustive list was not necessary included in the letter, and that failure to make corrections could result in “FDA initiating further action, including, but not limited to, civil money penalties, seizure, and/or injunction.”

JUUL has fifteen days to make corrections to its marketing programs, as well as to provide a written response to the FDA on the actions it has taken to correct the problems.

The full letter issued by the FDA to JUUL Labs can be found here.


Information for this briefing was found via the FDA. The author has no securities or affiliations related to any organization discussed. Not a recommendation to buy or sell. Always do additional research and consult a professional before purchasing a security. The author holds no licenses.

Video Articles

Silver Is in a New Price Regime, and the Market Isn’t Used to It | Keith Neumeyer – First Majestic

Agnico Eagle Just Made a Massive Gold Land Grab

A Copper-Gold Deposit Caught the White House’s Attention | Rob McLeod – Cambria Gold

Recommended

Mercado Drills 256 g/t Silver Over 6.5 Metres In First Drill Hole of Inaugural Program

Antimony Resources Drills 4.38% Sb Over 7.05 Metres At Bald Hill In Final Hole Of 2025 Program

Trending

Related News

Minnesota’s Lawsuit Against JUUL Labs Begins Trial

Minnesota Attorney General Keith Ellison opened his state’s case against e-cigarette maker Juul Labs on...

Wednesday, March 29, 2023, 04:07:00 PM

FDA Declares Lab-Grown Chicken Safe for Human Consumption

The US Food and Drug Administration (FDA) has approved lab-grown meat for human consumption, marking...

Thursday, November 17, 2022, 04:49:26 PM

Are Big Liquor And Tobacco Bankrolling Cannabis, Or Killing It?

Markets have been unkind to cannabis investors, and made certain fundamentals-based business bloggers, who were...

Saturday, June 6, 2020, 12:13:26 PM

FDA Releases Guidance for Psychedelic Drug Trials With Possibility of Removing Schedule I Classification

The U.S. Food and Drug Administration (FDA) has released a groundbreaking draft guidance to provide...

Tuesday, June 27, 2023, 03:03:00 PM

Biogen Wins Approval with FDA for Alzheimer’s Drug

This morning Biogen (NASDAQ:BIIB) received approval from the FDA for their Alzheimer’s drug aducanumab. The...

Monday, June 7, 2021, 11:49:16 AM