Product NDC: | 37000-801 |
Proprietary Name: | Vicks Sinex |
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: | 37000-801 |
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 NDC: | 37000-801-01 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (37000-801-01) > 15 mL in 1 BOTTLE, PUMP |
NDC Code | 37000-801-01 |
Proprietary Name | Vicks Sinex |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (37000-801-01) > 15 mL in 1 BOTTLE, PUMP |
Product NDC | 37000-801 |
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 | .000512 |
Strength Unit | g/mL |
Pharmaceutical Classes |