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: | 42002-201-05 |
Package Description: | 1 BOTTLE in 1 CARTON (42002-201-05) > 15 mL in 1 BOTTLE |
NDC Code | 42002-201-05 |
Proprietary Name | Visine A.C. |
Package Description | 1 BOTTLE in 1 CARTON (42002-201-05) > 15 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 |