Answer:
FDA regulations require that all medication labels include specific ingredients and possible side effects (option C).
Step-by-step explanation:
Food and Drug Administration (FDA) is an agency established in USA, in charge of the approval, regulation and surveillance of food and drugs for human and veterinary use, among other functions.
As part of the requirements that a drug needs for its marketing and use, the medication labels must contain the active ingredient and the possible adverse or side effects it may cause, for the knowledge of prescribing physicians and people who will use them.
The other options are not correct because:
- Price and manufacturing location is not information required by the FDA to be placed on the medication label.