
USFDA APPLICATION NUMBER - 19795 / DOSAGE - SOLUTION;TOPICAL - 0.5%
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| PODOFILOX(UNII: L36H50F353) (PODOFILOX - UNII:L36H50F353) | PODOFILOX | 5mg in 1 |
Inactive Ingredients
| Ingredient Name | Actavis Pharma, Inc. | Oceanside Pharmaceuticals |
|---|---|---|
| ALCOHOL(3K9958V90M) | ||
| LACTIC ACID, UNSPECIFIED FORM(33X04XA5AT) | ||
| SODIUM LACTATE(TU7HW0W0QT) |