Home
>
National Drug Code (NDC)
>
Alcortin A
Alcortin A - 68040-705-13 - (HYDROCORTISONE ACETATE, ALOE VERA LEAF and Iodoquinol)
Drug Information of Alcortin A
| Product NDC: | 68040-705 |
| Proprietary Name: | Alcortin A |
| Non Proprietary Name: | HYDROCORTISONE ACETATE, ALOE VERA LEAF and Iodoquinol |
| Active Ingredient(s): | 10; 20; 10 mg/g; mg/g; mg/g & nbsp; HYDROCORTISONE ACETATE, ALOE VERA LEAF and Iodoquinol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alcortin A
| Product NDC: | 68040-705 |
| Labeler Name: | Primus Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20100101 |
Package Information of Alcortin A
| Package NDC: | 68040-705-13 |
| Package Description: | 24 PACKET in 1 BOX (68040-705-13) > 1 g in 1 PACKET (68040-705-02) |
NDC Information of Alcortin A
| NDC Code | 68040-705-13 |
| Proprietary Name | Alcortin A |
| Package Description | 24 PACKET in 1 BOX (68040-705-13) > 1 g in 1 PACKET (68040-705-02) |
| Product NDC | 68040-705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCORTISONE ACETATE, ALOE VERA LEAF and Iodoquinol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Primus Pharmaceuticals |
| Substance Name | ALOE VERA LEAF; HYDROCORTISONE ACETATE; IODOQUINOL |
| Strength Number | 10; 20; 10 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
