Product NDC: | 33992-8685 |
Proprietary Name: | Assured Nasal Relief |
Non Proprietary Name: | OXYMETAZOLINE HYDROCHLORIDE |
Active Ingredient(s): | .05 mg/100mL & nbsp; OXYMETAZOLINE HYDROCHLORIDE |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 33992-8685 |
Labeler Name: | Greenbrier International, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130430 |
Package NDC: | 33992-8685-1 |
Package Description: | 1 BOTTLE in 1 TUBE (33992-8685-1) > 30 mL in 1 BOTTLE |
NDC Code | 33992-8685-1 |
Proprietary Name | Assured Nasal Relief |
Package Description | 1 BOTTLE in 1 TUBE (33992-8685-1) > 30 mL in 1 BOTTLE |
Product NDC | 33992-8685 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OXYMETAZOLINE HYDROCHLORIDE |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20130430 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Greenbrier International, Inc. |
Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
Strength Number | .05 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |