The Federal Pure Food and Drug Act of 1906 defined an adulterated drug as a drug that A. has false or misleading labeling. B. contains a decomposed substance or whose strength, quality, or purity is different

The Federal Pure Food and Drug Act of 1906 defined an adulterated drug as a drug that

A. has false or misleading labeling.
B. contains a decomposed substance or whose strength, quality, or purity is different from what's indicated on the label.
C. was prepared with alcohol or similar substances.
D. contains ergot, digitalis, or quinine

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