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Pramosone E
Pramosone E - 0496-0708-04 - (hydrocortisone acetate and pramoxine hydrochloride)
Drug Information of Pramosone E
| Product NDC: | 0496-0708 |
| Proprietary Name: | Pramosone E |
| Non Proprietary Name: | hydrocortisone acetate and pramoxine hydrochloride |
| Active Ingredient(s): | 25; 10 mg/g; mg/g & nbsp; hydrocortisone acetate and pramoxine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pramosone E
| Product NDC: | 0496-0708 |
| Labeler Name: | Ferndale Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100205 |
Package Information of Pramosone E
| Package NDC: | 0496-0708-04 |
| Package Description: | 28.4 g in 1 TUBE (0496-0708-04) |
NDC Information of Pramosone E
| NDC Code | 0496-0708-04 |
| Proprietary Name | Pramosone E |
| Package Description | 28.4 g in 1 TUBE (0496-0708-04) |
| Product NDC | 0496-0708 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone acetate and pramoxine hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100205 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Ferndale Laboratories, Inc. |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 25; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
