
USFDA APPLICATION NUMBER - 21844 / DOSAGE - GEL;TOPICAL - 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| DESONIDE(UNII: J280872D1O) (DESONIDE - UNII:J280872D1O) | DESONIDE | 0.5mg in 1 |
Inactive Ingredients
| Ingredient Name | LEO Pharma Inc. | Bayer HealthCare Pharmaceuticals Inc. |
|---|---|---|
| CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)(F68VH75CJC) | ||
| EDETATE DISODIUM(7FLD91C86K) | ||
| GLYCERIN(PDC6A3C0OX) | ||
| METHYLPARABEN(A2I8C7HI9T) | ||
| PROPYLENE GLYCOL(6DC9Q167V3) | ||
| PROPYLPARABEN(Z8IX2SC1OH) | ||
| SODIUM HYDROXIDE(55X04QC32I) | ||
| WATER(059QF0KO0R) |