Product NDC: | 64336-682 |
Proprietary Name: | Vicks |
Non Proprietary Name: | OXYMETAZOLINE HYDROCHLORIDE |
Active Ingredient(s): | .0005055 g/mL & nbsp; OXYMETAZOLINE HYDROCHLORIDE |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64336-682 |
Labeler Name: | Procter & Gamble Manufacturing GmbH |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090625 |
Package NDC: | 64336-682-01 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (64336-682-01) > 15 mL in 1 BOTTLE, SPRAY |
NDC Code | 64336-682-01 |
Proprietary Name | Vicks |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (64336-682-01) > 15 mL in 1 BOTTLE, SPRAY |
Product NDC | 64336-682 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OXYMETAZOLINE HYDROCHLORIDE |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20090625 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Procter & Gamble Manufacturing GmbH |
Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
Strength Number | .0005055 |
Strength Unit | g/mL |
Pharmaceutical Classes |