Other
Drug Facts
Extremely Flammable: Avoid fire, flame, or smoking during and immediately following application.
Distributed by:
Ohm Laboratories, Inc.
New Brunswick, NJ 08901
Product of Italy
The following Structured Product Label (SPL) was submitted to the FDA by Sun Pharmaceutical Industries, Inc. for the product Minoxidil (NDC 51672-2129). 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 other, active ingredient, purpose, use, warnings, do not use if, otc - ask doctor, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Extremely Flammable: Avoid fire, flame, or smoking during and immediately following application.
Distributed by:
Ohm Laboratories, Inc.
New Brunswick, NJ 08901
Product of Italy
Minoxidil 5% w/w (without propellant)
Hair regrowth treatment for women
to regrow hair on the top of the scalp (see pictures on side of this carton)
For external use only.
Ask a doctor before use if you have heart disease
May be harmful if used when pregnant or breast-feeding.
Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
butylated hydroxytoluene, cetyl alcohol, citric acid anhydrous, dehydrated alcohol, isobutane, lactic acid, n-butane, polysorbate 60, propane, purified water, stearyl alcohol
NDC 51672-2129-4
Minoxidil Topical Aerosol,
5% (For Women)
Two Month Supply
One 60 g (2.11 oz) Can
NDC 51672-2129-4
Two Month Supply
One 60 g (2.11 oz) Can
* Please review the disclaimer below.