Which item is NOT included on an OTC medicine label?

An OTC (over-the-counter) medicine label must adhere to specific guidelines set forth by the FDA, which is responsible for ensuring that these products meet standards for safety, efficacy, and labeling. However, while the label must comply with FDA regulations, it does not explicitly state the regulations themselves. Instead, it focuses on providing the consumer with essential information relevant to the safe and effective use of the medicine.

Included on an OTC medicine label are dosage instructions, which guide the user on how much and how often to take the medication. Active ingredients are clearly listed to inform consumers about what is in the product and how it functions. Additionally, warnings and side effects are crucial parts of the label, providing users with necessary cautions regarding potential adverse effects and interactions. These components help consumers make informed choices and use the medication safely.