Product NDC: | 64336-685 |
Proprietary Name: | Vicks |
Non Proprietary Name: | OXYMETAZOLINE HYDROCHLORIDE |
Active Ingredient(s): | .000512 g/mL & nbsp; OXYMETAZOLINE HYDROCHLORIDE |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64336-685 |
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: | 64336-685-01 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (64336-685-01) > 15 mL in 1 BOTTLE, PUMP |
NDC Code | 64336-685-01 |
Proprietary Name | Vicks |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (64336-685-01) > 15 mL in 1 BOTTLE, PUMP |
Product NDC | 64336-685 |
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 | .000512 |
Strength Unit | g/mL |
Pharmaceutical Classes |