USFDA APPLICATION NUMBER - 19968 / DOSAGE - OINTMENT;TOPICAL - 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
HALOBETASOL PROPIONATE(UNII: 91A0K1TY3Z) (HALOBETASOL - UNII:9P6159HM7T) | HALOBETASOL PROPIONATE | 0.5mg in 1 |
Inactive Ingredients
Ingredient Name | Ranbaxy Laboratories Inc. | Sun Pharmaceutical Industries, Inc. |
---|---|---|
ALUMINUM STEARATE(U6XF9NP8HM) | ||
CETYL ALCOHOL(936JST6JCN) | ||
DIAZOLIDINYL UREA(H5RIZ3MPW4) | ||
GLYCERIN(PDC6A3C0OX) | ||
ISOPROPYL ISOSTEARATE(C67IXB9Y7T) | ||
ISOPROPYL PALMITATE(8CRQ2TH63M) | ||
METHYLCHLOROISOTHIAZOLINONE(DEL7T5QRPN) | ||
METHYLISOTHIAZOLINONE(229D0E1QFA) | ||
MONOSTEARYL CITRATE(YWW937R1QR) | ||
PENTAERYTHRITOL(SU420W1S6N) | ||
PETROLATUM(4T6H12BN9U) | ||
PROPYLENE GLYCOL(6DC9Q167V3) | ||
SORBITAN SESQUIOLEATE(0W8RRI5W5A) | ||
STEARETH-21(53J3F32P58) | ||
WATER(059QF0KO0R) | ||
YELLOW WAX(2ZA36H0S2V) |
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