Product NDC: | 54868-5876 |
Proprietary Name: | Zeasorb |
Non Proprietary Name: | miconazole nitrate |
Active Ingredient(s): | 20.6 mg/g & nbsp; miconazole nitrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5876 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080331 |
Package NDC: | 54868-5876-0 |
Package Description: | 71 g in 1 BOTTLE (54868-5876-0) |
NDC Code | 54868-5876-0 |
Proprietary Name | Zeasorb |
Package Description | 71 g in 1 BOTTLE (54868-5876-0) |
Product NDC | 54868-5876 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | miconazole nitrate |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20080331 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 20.6 |
Strength Unit | mg/g |
Pharmaceutical Classes |