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USFDA APPLICATION NUMBER - 20805 / DOSAGE - SUSPENSION/DROPS;OTIC - EQ 0.2% BASE;1%
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| CIPROFLOXACIN HYDROCHLORIDE(UNII: 4BA73M5E37) (CIPROFLOXACIN - UNII:5E8K9I0O4U) | CIPROFLOXACIN | 2mg in 1 |
| HYDROCORTISONE(UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) | HYDROCORTISONE | 10mg in 1 |
Inactive Ingredients
| Ingredient Name | Alcon Laboratories, Inc. |
|---|---|
| ACETIC ACID(Q40Q9N063P) | |
| BENZYL ALCOHOL(LKG8494WBH) | |
| HYDROCHLORIC ACID(QTT17582CB) | |
| LECITHIN, SOYBEAN(1DI56QDM62) | |
| POLYSORBATE 20(7T1F30V5YH) | |
| POLYVINYL ALCOHOL(532B59J990) | |
| SODIUM ACETATE(4550K0SC9B) | |
| SODIUM CHLORIDE(451W47IQ8X) | |
| SODIUM HYDROXIDE(55X04QC32I) | |
| WATER(059QF0KO0R) |
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