USFDA APPLICATION NUMBER - 20762 / DOSAGE - SPRAY, METERED;NASAL - 0.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
MOMETASONE FUROATE MONOHYDRATE(UNII: MTW0WEG809) (Mometasone - UNII:8HR4QJ6DW8) | Mometasone | 50ug |
Inactive Ingredients
Ingredient Name | A-S Medication Solutions | Merck Sharp & Dohme Corp. | REMEDYREPACK INC. | Sandoz Inc. |
---|---|---|---|---|
BENZALKONIUM CHLORIDE(F5UM2KM3W7) | ||||
CARBOXYMETHYLCELLULOSE SODIUM(K679OBS311) | ||||
carboxymethylcellulose sodium, unspecified form(K679OBS311) | ||||
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||||
CITRIC ACID MONOHYDRATE(2968PHW8QP) | ||||
glycerin(PDC6A3C0OX) | ||||
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||||
polysorbate 80(6OZP39ZG8H) | ||||
SODIUM CITRATE(1Q73Q2JULR) | ||||
SODIUM CITRATE, UNSPECIFIED FORM(1Q73Q2JULR) |
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