Final answer:
The section on an Over-The-Counter product with usage directions is the “Drug Facts” label, standardized by the FDA for consumer safety.
Step-by-step explanation:
The name of the section on Over-The-Counter (OTC) products that includes the directions for use, among other information, is usually referred to as the “Drug Facts” label. This label is standardized by the Food and Drug Administration (FDA) and contains critical information such as active ingredients, uses (indications), warnings, directions for use, and other information like inactive ingredients. It is designed to help consumers make informed decisions and use the OTC medications safely and effectively. Ensuring that you read and understand the Drug Facts label is an essential step in the safe usage of any OTC medication.
The section on OTC products that includes the directions for use and other information is known as the Drug Facts section. The Drug Facts section is required by the FDA (Food and Drug Administration) for all over-the-counter drugs in the United States. It provides important information about the medication, including active ingredients, purpose, uses, warnings, dosage instructions, and more.