USFDA APPLICATION NUMBER - 21124 / DOSAGE - SOLUTION;TOPICAL - 1%
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
TERBINAFINE HYDROCHLORIDE(UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) | TERBINAFINE HYDROCHLORIDE | 1mL in 100 |
Inactive Ingredients
Ingredient Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | Novartis Consumer Health, Inc. |
---|---|---|
ALCOHOL(3K9958V90M) | ||
CETETH-20(I835H2IHHX) | ||
POLYOXYL 20 CETOSTEARYL ETHER(YRC528SWUY) | ||
PROPYLENE GLYCOL(6DC9Q167V3) | ||
WATER(059QF0KO0R) |
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