Active Ingredient
Minoxidil, USP 5% w/w (without propellant)
The following Structured Product Label (SPL) was submitted to the FDA by P & L Development, Llc for the product Minoxidil (NDC 59726-151). 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 active ingredient, purpose, use, warnings, do not use if, ask a doctor before use if you have, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Minoxidil, USP 5% w/w (without propellant)
Hair regrowth treatment for men
to regrow hair on the top of the scalp (vertex only, see pictures on side of carton)
For external use only. For use by men only.
Extremely Flammable: Avoid fire, flame, or smoking during and immediately following application.
heart disease
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
butane, butylated hydroxytoluene, cetyl alcohol, citric acid, glycerin, isobutane, lactic acid, polysorbate 60, propane, purified water, SD alcohol 40-B,stearyl alcohol
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
†Compare to the active ingredient in Men's Rogaine®
men's minoxidil Topical aerosol, 5%,
hair regrowth treatment
easy-to-use foam
not for use by women
g (oz) can
Read and keep carton and information leaflet for full product information.
†This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., distributor of Rogaine®.
Distributed by:
PL Developments
200 Hicks Street
Westbury, NY 11590
* Please review the disclaimer below.