| 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 |