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Under the FFDCA, the FDA is authorized to regulate products that constitute a combination of a drug, device, or biologic product.8 The agency has interpreted this provision as giving it the discretion to regulate combination products as drugs, as devices, or as biologic products.9 In its final rule, the FDA chose to regulate tobacco products under the device provisions of the FFDCA because they offer the agency greater regulatory flexibility than do the drug provisions of the act.10 The device authorities of the act present a range of regulatory controls that apply to all devices

Pouches usually offer the cleanest low-effort variety

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I went out to the sidewalk and smoked exactly one from the pack, which made me violently nauseated