| Product NDC: | 42002-201 |
| Proprietary Name: | Visine A.C. |
| Non Proprietary Name: | Tetrahydrozoline Hydrochloride and Zinc Sulfate |
| Active Ingredient(s): | .5; 2.5 mg/mL; mg/mL & nbsp; Tetrahydrozoline Hydrochloride and Zinc Sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42002-201 |
| Labeler Name: | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110916 |
| Package NDC: | 42002-201-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (42002-201-01) > 30 mL in 1 BOTTLE |
| NDC Code | 42002-201-01 |
| Proprietary Name | Visine A.C. |
| Package Description | 1 BOTTLE in 1 CARTON (42002-201-01) > 30 mL in 1 BOTTLE |
| Product NDC | 42002-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tetrahydrozoline Hydrochloride and Zinc Sulfate |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110916 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE |
| Strength Number | .5; 2.5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |