 
				 
										
USFDA APPLICATION NUMBER - 21862 / DOSAGE - SUSPENSION/DROPS;OPHTHALMIC - 0.1%
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength | 
|---|---|---|
| NEPAFENAC(UNII: 0J9L7J6V8C) (NEPAFENAC - UNII:0J9L7J6V8C) | NEPAFENAC | 1mg in 1 | 
Inactive Ingredients
| Ingredient Name | Alcon Laboratories, Inc. | 
|---|---|
| BENZALKONIUM CHLORIDE(F5UM2KM3W7) | |
| CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)(HHT01ZNK31) | |
| EDETATE DISODIUM(7FLD91C86K) | |
| HYDROCHLORIC ACID(QTT17582CB) | |
| MANNITOL(3OWL53L36A) | |
| SODIUM CHLORIDE(451W47IQ8X) | |
| SODIUM HYDROXIDE(55X04QC32I) | |
| TYLOXAPOL(Y27PUL9H56) | |
| WATER(059QF0KO0R) |