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: | 42002-204-35 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (42002-204-35) > 20 mL in 1 BOTTLE, PLASTIC |
NDC Code | 42002-204-35 |
Proprietary Name | Visine |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (42002-204-35) > 20 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 |