| Product NDC: | 42002-204 |
| Proprietary Name: | Visine |
| Non Proprietary Name: | Oxymetazoline Hydrochloride |
| Active Ingredient(s): | .25 mg/mL & nbsp; Oxymetazoline Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42002-204 |
| Labeler Name: | Johnson & Johnson Healthcare Products Inc., Division of McNEIL-PPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019407 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100405 |
| Package NDC: | 42002-204-05 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (42002-204-05) > 15 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 42002-204-05 |
| Proprietary Name | Visine |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (42002-204-05) > 15 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 42002-204 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20100405 |
| Marketing Category Name | NDA |
| Labeler Name | Johnson & Johnson Healthcare Products Inc., Division of McNEIL-PPC, Inc. |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |