Product NDC: | 0065-1431 |
Proprietary Name: | Systane Ultra |
Non Proprietary Name: | Polyethylene Glycol 400 and Propylene Glycol |
Active Ingredient(s): | 4; 3 mg/mL; mg/mL & nbsp; Polyethylene Glycol 400 and Propylene Glycol |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0065-1431 |
Labeler Name: | Alcon Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091130 |
Package NDC: | 0065-1431-05 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0065-1431-05) > 10 mL in 1 BOTTLE, DROPPER |
NDC Code | 0065-1431-05 |
Proprietary Name | Systane Ultra |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0065-1431-05) > 10 mL in 1 BOTTLE, DROPPER |
Product NDC | 0065-1431 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Polyethylene Glycol 400 and Propylene Glycol |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20091130 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Alcon Laboratories, Inc. |
Substance Name | POLYETHYLENE GLYCOL 400; PROPYLENE GLYCOL |
Strength Number | 4; 3 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |