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DermaCort
DermaCort - 54473-117-01 - (Hydrocortisone)
Drug Information of DermaCort
| Product NDC: | 54473-117 |
| Proprietary Name: | DermaCort |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 10 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DermaCort
| Product NDC: | 54473-117 |
| Labeler Name: | Melaleuca, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20000802 |
Package Information of DermaCort
| Package NDC: | 54473-117-01 |
| Package Description: | 28 g in 1 TUBE (54473-117-01) |
NDC Information of DermaCort
| NDC Code | 54473-117-01 |
| Proprietary Name | DermaCort |
| Package Description | 28 g in 1 TUBE (54473-117-01) |
| Product NDC | 54473-117 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20000802 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Melaleuca, Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
