Federal Pharmacy Law Practice Exam

The Food, Drug, and Cosmetic Act establishes essential standards for the labeling and dispensing of prescription drugs, emphasizing patient safety and accurate communication of essential information. One of the critical requirements is that prescription labels must include the patient's name and the doctor's name. This information is vital for ensuring that the medication is dispensed correctly to the intended patient and that it is associated with the approved prescribing physician.

Inclusion of the patient’s name helps pharmacists confirm the medication is appropriate for the individual, and it provides necessary identification in case of any questions or issues with the prescription. The doctor's name helps ensure the prescription is valid and tied to a licensed practitioner, enhancing accountability in the prescription process.

Other choices in this question address different aspects of drug labeling and usage but do not align with the specific requirements mandated by the Food, Drug, and Cosmetic Act as closely as including both the patient and doctor's names on the prescription label. Marks like optional expiration dates or lack of required package inserts do not enhance medication safety and proper dispensing, which is the focus of the law.