Other
Drug Facts
Distributed by:
Taro Pharmaceuticals U.S.A., Inc.
Hawthorne, NY 10532
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, extremely flammable, do not use if, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Distributed by:
Taro Pharmaceuticals U.S.A., Inc.
Hawthorne, NY 10532
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.
Avoid fire, flame, or smoking during and immediately following application.
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. 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
*Compare to the active
ingredient of
Women's Rogaine®
NDC 51672-2129-4
Minoxidil
Topical Aerosol,
5%
(For Women)
HAIR REGROWTH
TREATMENT
REACTIVATES
HAIR FOLLICLES
TO STIMULATE
REGROWTH
CLINICALLY
PROVEN TO
REGROW
HAIR
Once-a-Day
Foam
for Women
UNSCENTED
#1 DERMATOLOGIST
RECOMMENDED
ACTIVE INGREDIENT†
Two Month
Supply
One 60 g
(2.11 oz) Can
* Please review the disclaimer below.