Home > National Drug Code (NDC) > Advanced relief

Advanced relief - 51134-0064-5 - (dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl)

Alphabetical Index


Drug Information of Advanced relief

Product NDC: 51134-0064
Proprietary Name: Advanced relief
Non Proprietary Name: dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl
Active Ingredient(s): 1; 10; 10; .5    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl
Administration Route(s): OPHTHALMIC
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Advanced relief

Product NDC: 51134-0064
Labeler Name: Samchundang Pharm. Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100829

Package Information of Advanced relief

Package NDC: 51134-0064-5
Package Description: 1 BOTTLE in 1 BOX (51134-0064-5) > 15 mL in 1 BOTTLE

NDC Information of Advanced relief

NDC Code 51134-0064-5
Proprietary Name Advanced relief
Package Description 1 BOTTLE in 1 BOX (51134-0064-5) > 15 mL in 1 BOTTLE
Product NDC 51134-0064
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl
Dosage Form Name LIQUID
Route Name OPHTHALMIC
Start Marketing Date 20100829
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Samchundang Pharm. Co., Ltd.
Substance Name DEXTRAN 70; POLYETHYLENE GLYCOL 400; POVIDONE; TETRAHYDROZOLINE HYDROCHLORIDE
Strength Number 1; 10; 10; .5
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Advanced relief


General Information