
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) |