
USFDA APPLICATION NUMBER - 19716 / DOSAGE - LOTION, AUGMENTED;TOPICAL - EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| betamethasone dipropionate(UNII: 826Y60901U) (betamethasone - UNII:9842X06Q6M) | betamethasone | 0.5mg in 1 |
Inactive Ingredients
| Ingredient Name | Merck Sharp & Dohme Corp. |
|---|---|
| hydroxypropyl cellulose (1600000 WAMW)(RFW2ET671P) | |
| isopropyl alcohol(ND2M416302) | |
| phosphoric acid(E4GA8884NN) | |
| propylene glycol(6DC9Q167V3) | |
| sodium phosphate, monobasic, monohydrate(593YOG76RN) | |
| water(059QF0KO0R) |