Label: SUNHEAL 5% MINOXIDIL HAIR GROWTH KIT aerosol, foam
- NDC Code(s): 83462-019-01
- Packager: Eubizrival LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 1, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
-
DO NOT USE
■no one in your family has hair loss, but if you have hair loss is sudden or patchy or both.
■you don't know why your hair is falling out.
■you are under 18 years of age. Do not use it on babies and children.
■the scalp becomes red, inflamed, infected, inflamed, and painful.
■you are using other medicines on your scalp. - STOP USE
- ASK DOCTOR
- KEEP OOT OF REACH OF CHILDREN
-
DIRECTIONS
■Apply 1 pump of foam directly from the back of the crown to the frontal region.
■After massaging the scalp with your fingertips, wash your hands thoroughly. Using more of the hair growth foam or using it more often does not improve the results.
■Continued use is required to increase and maintain hair regrowth.
■Discontinuation may lead to hair loss. - OTHER INFORMATION
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SUNHEAL 5% MINOXIDIL HAIR GROWTH KIT
sunheal 5% minoxidil hair growth kit aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83462-019 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA FLOWER (UNII: 575DY8C1ER) HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW) (UNII: 2WID9OCG7P) ACETIC ACID (UNII: Q40Q9N063P) NIACINAMIDE (UNII: 25X51I8RD4) POLYSORBATE 20 (UNII: 7T1F30V5YH) POLYOXYL 50 HYDROGENATED CASTOR OIL (UNII: R07D3A9614) BIOTIN (UNII: 6SO6U10H04) WATER (UNII: 059QF0KO0R) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PANTHENOL (UNII: WV9CM0O67Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83462-019-01 60 g in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 04/01/2024 Labeler - Eubizrival LLC (036572203) Establishment Name Address ID/FEI Business Operations Eubizrival LLC 036572203 manufacture(83462-019) , label(83462-019)