| Product NDC: | 68788-9155 |
| Proprietary Name: | Nasal |
| Non Proprietary Name: | Oxymetazoline Hydrochloride |
| Active Ingredient(s): | 5 g/100mL & nbsp; Oxymetazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68788-9155 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090317 |
| Package NDC: | 68788-9155-3 |
| Package Description: | 30 mL in 1 BOTTLE, SPRAY (68788-9155-3) |
| NDC Code | 68788-9155-3 |
| Proprietary Name | Nasal |
| Package Description | 30 mL in 1 BOTTLE, SPRAY (68788-9155-3) |
| Product NDC | 68788-9155 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline Hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20090317 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |