Product NDC: | 65628-053 |
Proprietary Name: | FIRST Marys Mouthwash Compounding |
Non Proprietary Name: | Diphenhydramine Hydrochloride and Hydrocortisone and Nystatin and Tetracycline Hydrochloride |
Active Ingredient(s): | & nbsp; Diphenhydramine Hydrochloride and Hydrocortisone and Nystatin and Tetracycline Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65628-053 |
Labeler Name: | CutisPharma, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20101215 |
Package NDC: | 65628-053-01 |
Package Description: | 1 KIT in 1 CONTAINER (65628-053-01) * .06 g in 1 BOTTLE, GLASS * .45 g in 1 BOTTLE, GLASS * 1.2 g in 1 BOTTLE, GLASS * 1.5 g in 1 BOTTLE, GLASS * 234 mL in 1 BOTTLE, PLASTIC |
NDC Code | 65628-053-01 |
Proprietary Name | FIRST Marys Mouthwash Compounding |
Package Description | 1 KIT in 1 CONTAINER (65628-053-01) * .06 g in 1 BOTTLE, GLASS * .45 g in 1 BOTTLE, GLASS * 1.2 g in 1 BOTTLE, GLASS * 1.5 g in 1 BOTTLE, GLASS * 234 mL in 1 BOTTLE, PLASTIC |
Product NDC | 65628-053 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diphenhydramine Hydrochloride and Hydrocortisone and Nystatin and Tetracycline Hydrochloride |
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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