| Product NDC: | 65628-051 |
| Proprietary Name: | FIRST BXN Mouthwash |
| Non Proprietary Name: | Diphenhydramine, Lidocaine, Nystatin |
| Active Ingredient(s): | & nbsp; Diphenhydramine, Lidocaine, Nystatin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65628-051 |
| Labeler Name: | CutisPharma, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090908 |
| Package NDC: | 65628-051-01 |
| Package Description: | 1 KIT in 1 CONTAINER (65628-051-01) * .47 mL in 1 BOTTLE, GLASS * 236 mL in 1 BOTTLE, PLASTIC * .06 mL in 1 BOTTLE, GLASS * .47 mL in 1 BOTTLE, GLASS |
| NDC Code | 65628-051-01 |
| Proprietary Name | FIRST BXN Mouthwash |
| Package Description | 1 KIT in 1 CONTAINER (65628-051-01) * .47 mL in 1 BOTTLE, GLASS * 236 mL in 1 BOTTLE, PLASTIC * .06 mL in 1 BOTTLE, GLASS * .47 mL in 1 BOTTLE, GLASS |
| Product NDC | 65628-051 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diphenhydramine, Lidocaine, Nystatin |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20090908 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | CutisPharma, Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |