Suggested talking points:
- since e-cigarettes (nicotine vaporizers) are derived from tobacco, the FDA can legally reclassify and regulate them as "tobacco products",
- by choosing to classify e-cigarettes as "drugs" or "devices", the FDA was/is attempting to ban the products,
- hundreds of thousands of smokers already have significantly reduced their health risks by switching to e-cigarettes,
- by reclassifying e-cigarettes as tobacco products, the FDA would ban their sale to minors, can establish other reasonable and responsible product regulations, would help to reduce (instead of maintain) cigarette consumption, and would save taxpayers money that FDA continues to waste,
- in SE vs FDA, federal Judge Richard Leon has ruled that the FDA can regulate e-cigarettes as "tobacco products", but not as "drugs" or "devices",
- sales and use of e-cigarettes have continued to sharply increase despite the FDA's ongoing attempt to ban the products,
- banning e-cigarettes would primarily protect cigarette markets at the expense of consumer and public health,
- if applicable, describe your personal experience using e-cigarettes.
