Which of the following is TRUE with regard to the FDA and supplement manufacturing?
A) The FDA is responsible for regulating health claims made in advertising dietary supplements.
B) Structure/function claims do not require FDA approval, but the manufacturer must provide the FDA with the text of the claim within 30 days of putting the product on the market.
C) Supplement companies are required to report all adverse events to the FDA.
D) The FDA Manufacturers must provide FDA with evidence of product's safety and efficacy based on clinical trials.
B
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The platelet function analyzer standardized the bleeding time method by eliminating the variables of the method. Which of the following represents the variables of bleeding time?
a. Dependence on the presence of calcium b. Ingestion of aspirin c. Room temperature, depth, location and direction of the incision; movement of the arm, and laboratician experience d. Abnormal platelet count
A cold sore or fever blister around the lips is a form of Herpes simplex II.
Answer the following statement true (T) or false (F)