RICHMOND, Va., October 22, 2019 /PRNewswire/ -- In a historic decision, the U.S. Food & Drug Administration authorized Swedish Match U.S. Division's amended Modified Risk Tobacco Product applications (MRTPAs) for eight varieties of General Snus, making it the first tobacco product to secure the modified risk designation and right to market the product as a less harmful alternative to cigarettes.
"Today's decision is a huge accomplishment for public health in the U.S. and another step toward realizing our vision of a world without cigarettes," said Gerry Roerty, Vice President and General Counsel. "There are nearly 35 million adult smokers in the U.S., all of which have been led to believe the only way to reduce tobacco risk is complete abstinence. We now have the opportunity and responsibility to inform cigarette users who cannot abstain that General Snus can be a risk-reducing alternative. If that's enough to make even a percentage of them switch, we've made progress."
The modified risk status classifies General Snus as a tobacco product that is sold or distributed for use to reduce harm or the risk of tobacco-related disease associated with commercially marketed tobacco products. The FDA also cleared Swedish Match's claim that using General Snus instead of cigarettes puts users at a lower risk of mouth cancer, heart disease, lung cancer, stroke, emphysema and chronic bronchitis.
The authorized claim allows Swedish Match to begin working to reduce misperceptions related to the risk of General Snus. According to the National Young Adult Health Survey, only 10 percent of respondents believed snus was less risky than cigarettes.
General Snus has already been tied to progressing the reduction of cigarette use in other countries. In Sweden, widespread use of snus in place of cigarettes is believed to have helped the country achieve the lowest lung and oral cancer rates in men in Europe. In Norway, snus rates among young women increased to 13 percent since its legalization in 2002. Smoking rates among young women dropped from 30 percent in 2001 to one percent in the almost exact same time span.
"Few products have a proven track record like General Snus," added Roerty. "And while we're hopeful it will benefit the U.S. population just as it's benefited Norway and Sweden, we want to be clear that General Snus reduces risk for individuals who use tobacco products. No tobacco product, including General Snus, is completely harmless, which is why youth and non-tobacco users should not use it in the first place. Our goal is to help adult smokers by educating them, not attract new users."
Swedish Match sold its cigarette business in 1999, choosing instead to focus on alternative products believed to be less harmful. Fifteen years later, it became the first company to successfully submit MRTPAs, which was partially rejected by the FDA in 2016. The FDA's approval of the amended version comes on the heels of the 20th anniversary of Swedish Match's divestiture of its cigarette business.
Swedish Match was also the first to receive FDA approval for its Premarket Tobacco Application (PMTA) for General Snus in November 2015. The FDA ruled enough evidence demonstrated that the product was appropriate for the protection of public health.
General Snus, which originated in Sweden 153 years ago, is a smokeless, spitless tobacco product placed in the upper lip. It contains four ingredients: tobacco, water, table salt and flavorings, such as mint or bergamot oil.
For further information, please contact: Sandy Fowler-Jones Director of Communications 804-363-0424 (cell) 804-787-5132 (office)