| Product NDC: | 63736-663 |
| Proprietary Name: | Privine |
| Non Proprietary Name: | Naphazoline Hydrochloride |
| Active Ingredient(s): | .125 mL/25mL & nbsp; Naphazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63736-663 |
| Labeler Name: | Insight Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090716 |
| Package NDC: | 63736-663-01 |
| Package Description: | 1 BOTTLE in 1 BOX (63736-663-01) > 25 mL in 1 BOTTLE |
| NDC Code | 63736-663-01 |
| Proprietary Name | Privine |
| Package Description | 1 BOTTLE in 1 BOX (63736-663-01) > 25 mL in 1 BOTTLE |
| Product NDC | 63736-663 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naphazoline Hydrochloride |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | NASAL |
| Start Marketing Date | 20090716 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals LLC |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE |
| Strength Number | .125 |
| Strength Unit | mL/25mL |
| Pharmaceutical Classes |