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Vicks Sinex
Vicks Sinex - 37000-802-01 - (Oxymetazoline Hydrochloride)
Drug Information of Vicks Sinex
| Product NDC: | 37000-802 |
| Proprietary Name: | Vicks Sinex |
| Non Proprietary Name: | Oxymetazoline Hydrochloride |
| Active Ingredient(s): | .0005095 g/mL & nbsp; Oxymetazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vicks Sinex
| Product NDC: | 37000-802 |
| Labeler Name: | The Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100706 |
Package Information of Vicks Sinex
| Package NDC: | 37000-802-01 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (37000-802-01) > 15 mL in 1 BOTTLE, PUMP |
NDC Information of Vicks Sinex
| NDC Code | 37000-802-01 |
| Proprietary Name | Vicks Sinex |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (37000-802-01) > 15 mL in 1 BOTTLE, PUMP |
| Product NDC | 37000-802 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline Hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20100706 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Procter & Gamble Manufacturing Company |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .0005095 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
