prescriptionrequired

Prescription required is a regulatory designation for products that may only be obtained or used with a prescription from a licensed health professional. The designation is most commonly applied to medicines intended to diagnose, treat, or prevent illness, but can also apply to certain medical devices or diagnostic products in some jurisdictions. The purpose is to ensure professional evaluation, appropriate dosing, and monitoring for safety and effectiveness, reducing risks such as adverse reactions, drug interactions, and misuse.

Most regulatory frameworks divide products into over-the-counter and prescription-only categories. Examples of prescription-only medicines include antibiotics, many antidepressants and antipsychotics, hormonal therapies (such as birth control), cardiovascular drugs, opioids, and vaccines in some systems. Some countries also use behind-the-counter medicines that require pharmacist consultation but not a physician’s prescription.

Regulatory authorities such as the U.S. Food and Drug Administration, the European Medicines Agency, and national agencies determineRx status within their jurisdictions. Labeling and terminology vary: many places use “Rx only” or equivalent to indicate prescription status, while others use local terms such as “POM” (prescription-only medicine) or similar phrases. The designation may apply only to the medicine itself, or to specific strengths, formulations, or routes of administration.

Obtaining a prescription typically involves clinical assessment by a licensed professional, followed by a written or electronic prescription and verification at a pharmacy. Pharmacists may provide counseling and check for drug interactions, allergies, and suitability before dispensing the product.

Prescription requirements aim to balance safe, effective treatment with access considerations, recognizing that the need for professional oversight can affect timely access and health equity.