Other
Drug Facts
DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OH 45202
The following Structured Product Label (SPL) was submitted to the FDA by Kroger Company for the product Minoxidil (NDC 59450-211). 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 THE KROGER CO.
CINCINNATI, OH 45202
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
IN WOMEN'S ROGAINE®*
NDC 59450-211-02
Kroger®
*SEE SIDE
PANEL
#1 DERMATOLOGIST RECOMMENDED
ACTIVE INGREDIENT†
ONCE-A-DAY FOAM
Minoxidil
Topical Aerosol, 5%
(For Women)
Hair Regrowth Treatment
CLINICALLY PROVEN
TO REGROW HAIR
REACTIVATES HAIR FOLLICLES
TO STIMULATE REGROWTH
UNSCENTED
FOUR MONTH SUPPLY
TWO 60 g (2.11 OZ) CANS
TOTAL 120 g (4.22 OZ)
* Please review the disclaimer below.