| 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 |