Home > National Drug Code (NDC) > REFRESH OPTIVE Advanced

REFRESH OPTIVE Advanced - 0023-4307-03 - (carboxymethylcellulose sodium, glycerin, and polysorbate 80)

Alphabetical Index


Drug Information of REFRESH OPTIVE Advanced

Product NDC: 0023-4307
Proprietary Name: REFRESH OPTIVE Advanced
Non Proprietary Name: carboxymethylcellulose sodium, glycerin, and polysorbate 80
Active Ingredient(s): 5; 10; 5    mg/mL; mg/mL; mg/mL & nbsp;   carboxymethylcellulose sodium, glycerin, and polysorbate 80
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of REFRESH OPTIVE Advanced

Product NDC: 0023-4307
Labeler Name: Allergan, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111130

Package Information of REFRESH OPTIVE Advanced

Package NDC: 0023-4307-03
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0023-4307-03) > 3 mL in 1 BOTTLE, DROPPER

NDC Information of REFRESH OPTIVE Advanced

NDC Code 0023-4307-03
Proprietary Name REFRESH OPTIVE Advanced
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0023-4307-03) > 3 mL in 1 BOTTLE, DROPPER
Product NDC 0023-4307
Product Type Name HUMAN OTC DRUG
Non Proprietary Name carboxymethylcellulose sodium, glycerin, and polysorbate 80
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20111130
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Allergan, Inc.
Substance Name CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80
Strength Number 5; 10; 5
Strength Unit mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of REFRESH OPTIVE Advanced


General Information