Swedish Match tries again

The US Food and Drug Administration said yesterday it had posted an amendment to the modified risk tobacco product applications (MRTPAs) for General Snus products submitted by Swedish Match North America.
The FDA said that, on December 14, 2016, it had denied the company’s request ‘to remove a currently required warning statement that products can cause gum disease and tooth loss’.
‘With respect to the company’s other requests to remove or revise two additional currently required warnings, FDA deferred final action and issued a response that offered the company an option to amend its applications,’ it said in a note issued through the Center for Tobacco Products.
‘FDA will post any future amendments to the application on the Center for Tobacco Products’ website on a rolling basis as the materials are redacted.’
More information is available here.