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Visine Original
Visine Original - 42002-203-35 - (Tetrahydrozoline Hydrochloride)
Drug Information of Visine Original
| Product NDC: | 42002-203 |
| Proprietary Name: | Visine Original |
| Non Proprietary Name: | Tetrahydrozoline Hydrochloride |
| Active Ingredient(s): | .5 mg/mL & nbsp; Tetrahydrozoline Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Visine Original
| Product NDC: | 42002-203 |
| 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: | 20110825 |
Package Information of Visine Original
| Package NDC: | 42002-203-35 |
| Package Description: | 1 BOTTLE in 1 CARTON (42002-203-35) > 19 mL in 1 BOTTLE |
NDC Information of Visine Original
| NDC Code | 42002-203-35 |
| Proprietary Name | Visine Original |
| Package Description | 1 BOTTLE in 1 CARTON (42002-203-35) > 19 mL in 1 BOTTLE |
| Product NDC | 42002-203 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tetrahydrozoline Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110825 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | TETRAHYDROZOLINE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
