Medications, supplements, or health-related products available for purchase without a prescription, providing convenient access for consumers to address common health needs.
The chemical component in an OTC product responsible for its therapeutic effects, prominently listed on the product packaging.
The recommended amount of an OTC medication or supplement to be taken at one time or over a specific period, outlined in the product’s instructions.
Components in an OTC product that do not contribute to its therapeutic effects but may include fillers, flavorings, or colorings.
The commercial name given to an OTC product by the manufacturer, often used for marketing purposes, distinct from the generic name.
The official, non-proprietary name of the active ingredient in an OTC product, commonly used in place of the brand name.
Guidelines provided on OTC product labels, specifying how often and in what quantity the product should be taken for optimal effectiveness.
The date printed on OTC product packaging, indicating the period during which the product is guaranteed to remain safe and effective.
Unexpected or harmful effects experienced by individuals using an OTC product, prompting them to seek medical attention if necessary.
Effects that occur when an OTC medication or supplement interacts with another substance, such as prescription drugs, food, or other OTC products.
Unintended, often mild effects of an OTC product that may occur in addition to its therapeutic benefits, usually listed on the product label.
Substances in OTC products that may cause an allergic reaction in some individuals, often clearly labeled to alert consumers.