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USFDA APPLICATION NUMBER - 22013 / DOSAGE - AEROSOL, FOAM;TOPICAL - 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| CLOBETASOL PROPIONATE(UNII: 779619577M) (CLOBETASOL - UNII:ADN79D536H) | CLOBETASOL PROPIONATE | 0.5mg in 1 |
Inactive Ingredients
| Ingredient Name | Prestium Pharma, Inc. | Renaissance Pharma, Inc. |
|---|---|---|
| ANHYDROUS CITRIC ACID(XF417D3PSL) | ||
| CETYL ALCOHOL(936JST6JCN) | ||
| CYCLOMETHICONE(NMQ347994Z) | ||
| ISOPROPYL MYRISTATE(0RE8K4LNJS) | ||
| LIGHT MINERAL OIL(N6K5787QVP) | ||
| PETROLATUM(4T6H12BN9U) | ||
| PHENOXYETHANOL(HIE492ZZ3T) | ||
| POLYOXYL 20 CETOSTEARYL ETHER(YRC528SWUY) | ||
| POTASSIUM CITRATE(EE90ONI6FF) | ||
| PROPYLENE GLYCOL(6DC9Q167V3) | ||
| SORBITAN MONOLAURATE(6W9PS8B71J) | ||
| WATER(059QF0KO0R) |
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