FDA Reviews TJP Labs' L!X Nicotine Pouch Product Application

FDA Reviews TJP Labs' L!X Nicotine Pouch Product Application
FDA reviewing TJP Labs' L!X nicotine pouch for adult smokers who seek safer alternative to combustible tobacco products.

The US Food and Drug Administration (FDA) has accepted a pre-market tobacco product application from TJP Labs for its L!X nicotine pouch product for review.

TJP Labs has created the L!X nicotine pouch for adult users (21 years and older) who are unable or unwilling to quit using nicotine products, particularly those who wish to transition to non-combustible oral products, according to a statement by TJP Labs CEO David Richmond-Peck.

He said, "The acceptance of our application by the FDA shows our team's dedication to providing alternative products for adult users that may reduce harm associated with traditional combustible tobacco products. Our factory's Canadian Health Department drug establishment license (DEL), natural health product site license, ISO 9001:2015, HACCP, and cGMP certifications demonstrate TJP Labs' strict quality standards and will further enhance our ability to serve the high-volume international market.

TJP Labs is a top-tier full-service contract manufacturer for next-generation products, specializing in oral nicotine pouches, caffeine, and other health supplements delivery solutions. The company is headquartered in Pickering, Ontario, Canada.

The L!X nicotine pouches are sold by L!X Innovations, a subsidiary of TJP Lab.

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