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