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 | |
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