What information must be included on the label of a non-controlled substance prescription container?

The correct choice emphasizes the importance of labeling transparency and safety in pharmaceutical practices. The name of the manufacturer and distributor must be included on the label to ensure that patients and healthcare providers can identify the source of the medication. This information is critical for a couple of reasons: it allows for the tracking of medication in the event of recalls, helps to ensure that patients receive the correct product, and provides valuable information about the drug's origin, which might be relevant in case of side effects or allergic reactions.

The other elements, such as the name and address of the patient, date the prescription was dispensed, and the serum number of the prescription, although crucial in their own right for various safety and legal reasons, are not the primary focus in the context of identifying the source or accountability of pharmaceutical products. This highlights the regulatory emphasis on ensuring proper identification and traceability of drugs through their manufacturers and distributors.