What must labels of nonprescription drug products for oral use indicate?

The requirement for labeling nonprescription drug products for oral use focuses on providing essential information that consumers need to make informed decisions about using the product. One key aspect of this is indicating the total sodium content. This is particularly important because excessive sodium intake can have health implications, such as contributing to hypertension and other cardiovascular issues. By including total sodium content on labels, manufacturers ensure that consumers are aware of the amount of sodium in the product, allowing those who are monitoring their sodium intake—such as individuals with specific dietary restrictions or health conditions—to make safer choices.

In contrast, while total sugar content, total volume, and total active ingredients are important pieces of information, they are not specifically mandated for all nonprescription oral drug products in the same way total sodium content is, particularly regarding dietary concerns.