Minoxidil
FDA Label NDC 85524-2501

The following Structured Product Label (SPL) was submitted to the FDA by Flexigo Inc for the product Minoxidil (NDC 85524-2501). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding for external use only.when using this product, avoidgetting into eyes. lf contact occurs, rinse thoroughlywith water. lfskin irritation occurs, wash product offand consult a physician.when first applying thisproduct,you may experience a slight tingling sensation.this is an indication that the product is working. lf thesensation is prolonged or becomes unpleasant,discontinue use and consult a physician., avoid contact with eyes. lf the product gets into the eye,flush with water for 15 minutes. avoid inhaling vapors. cap the bottle tightly. out of direct sunlight and store at room temperature away from heat., you become pregnant, or are planning to become pregnant, while using the product. if discomfort persists., vitamin c, for external use only., dosage & administration, inactive ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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