Product NDC: | 37808-065 |
Proprietary Name: | rx act nasal |
Non Proprietary Name: | Oxymetazoline HCl |
Active Ingredient(s): | .05 g/100mL & nbsp; Oxymetazoline HCl |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37808-065 |
Labeler Name: | H E B |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19951012 |
Package NDC: | 37808-065-10 |
Package Description: | 1 BOTTLE in 1 CARTON (37808-065-10) > 30 mL in 1 BOTTLE |
NDC Code | 37808-065-10 |
Proprietary Name | rx act nasal |
Package Description | 1 BOTTLE in 1 CARTON (37808-065-10) > 30 mL in 1 BOTTLE |
Product NDC | 37808-065 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Oxymetazoline HCl |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 19951012 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H E B |
Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
Strength Number | .05 |
Strength Unit | g/100mL |
Pharmaceutical Classes |