Home > National Drug Code (NDC) > Advanced Eye Relief/ Redness Instant Relief

Advanced Eye Relief/ Redness Instant Relief - 24208-349-75 - (Naphazoline Hydrochloride and Polyethylene glycol 300)

Alphabetical Index


Drug Information of Advanced Eye Relief/ Redness Instant Relief

Product NDC: 24208-349
Proprietary Name: Advanced Eye Relief/ Redness Instant Relief
Non Proprietary Name: Naphazoline Hydrochloride and Polyethylene glycol 300
Active Ingredient(s): .1; 2    mg/mL; mg/mL & nbsp;   Naphazoline Hydrochloride and Polyethylene glycol 300
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Advanced Eye Relief/ Redness Instant Relief

Product NDC: 24208-349
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100913

Package Information of Advanced Eye Relief/ Redness Instant Relief

Package NDC: 24208-349-75
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-349-75) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of Advanced Eye Relief/ Redness Instant Relief

NDC Code 24208-349-75
Proprietary Name Advanced Eye Relief/ Redness Instant Relief
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-349-75) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 24208-349
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naphazoline Hydrochloride and Polyethylene glycol 300
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20100913
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Bausch & Lomb Incorporated
Substance Name NAPHAZOLINE HYDROCHLORIDE; POLYETHYLENE GLYCOL 300
Strength Number .1; 2
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Advanced Eye Relief/ Redness Instant Relief


General Information