US FDA issues 'Modified Risk Tobacco Product Orders' for 20 ZYN Nicotine pouch products
New Delhi, July 3 -- Philip Morris International Inc. (PMI) (NYSE: PM) announced that the U.S. Food and Drug Administration (FDA) issued Modified Risk Tobacco Product (MRTP) orders for 20 variants of ZYN nicotine pouch products. These are the first MRTP orders granted for nicotine pouches, allowing PMI U.S. to market the following claim for the authorized ZYN products: "Using ZYN instead of cigarettes puts you at a lower risk of mouth cancer, heart disease, lung cancer, stroke, emphysema, and chronic bronchitis."
"FDA's decision is an important moment for the more than 45 million legal-age nicotine consumers in America," said Stacey Kennedy, PMI U.S. CEO. "Today's news ensures these adults have access to accurate, science-based informati...
Click here to read full article from source
To read the full article or to get the complete feed from this publication, please
Contact Us.