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Original Redness Reliever - 11822-3215-3 - (Naphazoline Hydrochloride and Polyethylene glycol 300)

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Drug Information of Original Redness Reliever

Product NDC: 11822-3215
Proprietary Name: Original Redness Reliever
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 Original Redness Reliever

Product NDC: 11822-3215
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100913

Package Information of Original Redness Reliever

Package NDC: 11822-3215-3
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (11822-3215-3) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of Original Redness Reliever

NDC Code 11822-3215-3
Proprietary Name Original Redness Reliever
Package Description 1 BOTTLE, DROPPER in 1 CARTON (11822-3215-3) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 11822-3215
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 Rite Aid Corporation
Substance Name NAPHAZOLINE HYDROCHLORIDE; POLYETHYLENE GLYCOL 300
Strength Number .1; 2
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Original Redness Reliever


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