Which information must be included on a non-prescription drug label?

The inclusion of the name of the product along with the name and address of the manufacturer on a non-prescription drug label is essential for several reasons. Firstly, it helps ensure clear identification of the product, which is crucial for consumers to understand what they are purchasing. The product's name provides immediate recognition, while the manufacturer's information allows consumers to verify the source and credibility of the product, which can be especially important in cases of recalls or safety concerns.

Furthermore, regulatory agencies like the FDA require this information as part of labeling standards to promote safety and efficacy in non-prescription medications. This guideline helps consumers make informed decisions about their health and aligns with safety protocols that ensure accountability from manufacturers.

In contrast, while side effects information is important, it is not feasible for all possible side effects to be listed on the label due to space constraints and variations in individuals’ reactions. The price of the drug, while useful for consumers, is not a mandatory component of the label according to FDA regulations. Lastly, availability information is typically not included on the label itself, as it can change frequently and is not directly related to the product’s safety or efficacy. Thus, the correct answer emphasizes the critical details that promote informed consumer choice and accountability in the pharmaceutical market