| Product NDC: | 65628-052 |
| Proprietary Name: | FIRST Dukes Mouthwash Compounding |
| Non Proprietary Name: | Diphenhydramine Hydrochloride and Hydrocortisone and Nystatin |
| Active Ingredient(s): | & nbsp; Diphenhydramine Hydrochloride and Hydrocortisone and Nystatin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65628-052 |
| Labeler Name: | CutisPharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101215 |
| Package NDC: | 65628-052-01 |
| Package Description: | 1 KIT in 1 CONTAINER (65628-052-01) * .06 g in 1 BOTTLE, GLASS * .525 g in 1 BOTTLE, GLASS * .6 g in 1 BOTTLE, GLASS * 234 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 65628-052-01 |
| Proprietary Name | FIRST Dukes Mouthwash Compounding |
| Package Description | 1 KIT in 1 CONTAINER (65628-052-01) * .06 g in 1 BOTTLE, GLASS * .525 g in 1 BOTTLE, GLASS * .6 g in 1 BOTTLE, GLASS * 234 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 65628-052 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride and Hydrocortisone and Nystatin |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20101215 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | CutisPharma, Inc. |
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