U.S. FDA says it needs more time to decide on Juul, other e-cigarettes

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U.S. FDA says it needs more time to decide on Juul, other e-cigarettes
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The U.S. Food and Drug Administration said on Thursday it needs more time to decide whether e-cigarette maker Juul Labs Inc and other major manufacturers can sell their products in the United States.

Blu, faced a deadline to file applications showing their products provided a net benefit to public health.

It said products that have not been authorized by the FDA - a category that now includes Juul after the one-year grace period - "are subject to enforcement action at the FDA's discretion." During that time, Juul and dozens of competitors introduced products that were grandfathered into the market because they were already being sold before the regulation took effect.

In June, FDA acting Commissioner Dr. Janet Woodcock told a congressional panel the agency had received applications for 6.5 million products from more than 550 companies, and said reviewing all submissions by Sept. 9 "will be challenging." A Reuters investigation in 2019 detailed how Juul’s developers used tobacco industry research and patents to formulate a smooth but potent blend of liquid nicotine that became a key factor in its popularity among teenagers.

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