Product NDC: | 67172-292 |
Proprietary Name: | Clear Eyes Cooling Itchy Eye Relief |
Non Proprietary Name: | Naphazoline Hydrochloride and Glycerin and Zinc Sulfate |
Active Ingredient(s): | .0025; .00012; .0025 mg/mL; mg/mL; mg/mL & nbsp; Naphazoline Hydrochloride and Glycerin and Zinc Sulfate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67172-292 |
Labeler Name: | Prestige Brands Holdings, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110215 |
Package NDC: | 67172-292-01 |
Package Description: | 1 BOTTLE, DROPPER in 1 BOX (67172-292-01) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 67172-292-01 |
Proprietary Name | Clear Eyes Cooling Itchy Eye Relief |
Package Description | 1 BOTTLE, DROPPER in 1 BOX (67172-292-01) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 67172-292 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Naphazoline Hydrochloride and Glycerin and Zinc Sulfate |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110215 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Prestige Brands Holdings, Inc. |
Substance Name | GLYCERIN; NAPHAZOLINE HYDROCHLORIDE; ZINC SULFATE |
Strength Number | .0025; .00012; .0025 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |