Product NDC: | 67172-595 |
Proprietary Name: | Clear Eyes Complete 7 Symptom Relief |
Non Proprietary Name: | Hypromellose and Naphazoline Hydrochloride and Polysorbate 80 and Zinc Sulfate |
Active Ingredient(s): | .5; .0625; 1.25; .625 mL/mL; mL/mL; mL/mL; mL/mL & nbsp; Hypromellose and Naphazoline Hydrochloride and Polysorbate 80 and Zinc Sulfate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67172-595 |
Labeler Name: | Prestige Brands Holdings, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100301 |
Package NDC: | 67172-595-01 |
Package Description: | 1 BOTTLE, DROPPER in 1 BOX (67172-595-01) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 67172-595-01 |
Proprietary Name | Clear Eyes Complete 7 Symptom Relief |
Package Description | 1 BOTTLE, DROPPER in 1 BOX (67172-595-01) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 67172-595 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Hypromellose and Naphazoline Hydrochloride and Polysorbate 80 and Zinc Sulfate |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20100301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Prestige Brands Holdings, Inc. |
Substance Name | HYPROMELLOSE; NAPHAZOLINE HYDROCHLORIDE; POLYSORBATE 80; ZINC SULFATE |
Strength Number | .5; .0625; 1.25; .625 |
Strength Unit | mL/mL; mL/mL; mL/mL; mL/mL |
Pharmaceutical Classes |