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Stimulated salivary flow rate, pH and lactobacillus and yeast concentrations in non-smokers and smokers

The Family Smoking Prevention and Tobacco Control Act, the statute that gave the FDA authority over tobacco products, defines them as products "made or derived from tobacco that [are] intended for human consumption, including any component, part, or accessory of a tobacco product." In deeming e-cigarettes to be tobacco products, the FDA defined "component or part" as "any software or assembly of materials intended or reasonably expectedto alter or affect the tobacco product's performance, composition, constituents, or characteristics" or "to be used with or for the human consumption of a tobacco product." Hence vaping equipment, whether a closed, disposable e-cigarette or an open system with a refillable tank and parts that can be switched out, is a "component or part" of a tobacco product, which means it is also a tobacco product

ACKNOWLEDGEMENTS This research has been conducted using the UK Biobank Resource under Application Number 55917

The Act was repealed in 1998 as part of a wider rationalisation of English statute law, but later anti-slavery legislation remains in force.

The clean, slightly grassy sweetness with a smooth finish is the benchmark