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REFRESH OPTIVE Advanced - 0023-4491-30 - (carboxymethylcellulose sodium, glycerin, polysorbate 80)

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Drug Information of REFRESH OPTIVE Advanced

Product NDC: 0023-4491
Proprietary Name: REFRESH OPTIVE Advanced
Non Proprietary Name: carboxymethylcellulose sodium, glycerin, polysorbate 80
Active Ingredient(s): 5; 10; 5    mg/mL; mg/mL; mg/mL & nbsp;   carboxymethylcellulose sodium, glycerin, 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: 0023-4491
Labeler Name: Allergan, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130115

Package Information of REFRESH OPTIVE Advanced

Package NDC: 0023-4491-30
Package Description: 30 VIAL, SINGLE-USE in 1 CARTON (0023-4491-30) > .4 mL in 1 VIAL, SINGLE-USE

NDC Information of REFRESH OPTIVE Advanced

NDC Code 0023-4491-30
Proprietary Name REFRESH OPTIVE Advanced
Package Description 30 VIAL, SINGLE-USE in 1 CARTON (0023-4491-30) > .4 mL in 1 VIAL, SINGLE-USE
Product NDC 0023-4491
Product Type Name HUMAN OTC DRUG
Non Proprietary Name carboxymethylcellulose sodium, glycerin, polysorbate 80
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20130115
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


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