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FDAs MRTP review framework is informed by its March 2012 draft guidance, Modified Risk Tobacco Product Applications , which remains FDAs operative guidance on the content and organization of MRTP applications and calls for a broad scientific showing addressing, among other things, product characterization, nonclinical and clinical evidence, consumer perception and understanding, actual-use behavior, population-level modeling, proposed labeling and advertising, and postmarket surveillance

Some caucus members warned that banning menthol would create an illegal market for the products, subjecting Black communities to increased law enforcement