Home
>
National Drug Code (NDC)
>
Terapie Callus Remover
Terapie Callus Remover - 10849-001-01 - (SALICYLIC ACID)
Drug Information of Terapie Callus Remover
| Product NDC: | 10849-001 |
| Proprietary Name: | Terapie Callus Remover |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 17 mL/100mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Terapie Callus Remover
| Product NDC: | 10849-001 |
| Labeler Name: | Armand Dupree |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358F |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111104 |
Package Information of Terapie Callus Remover
| Package NDC: | 10849-001-01 |
| Package Description: | 1 TUBE in 1 CARTON (10849-001-01) > 7.5 mL in 1 TUBE |
NDC Information of Terapie Callus Remover
| NDC Code | 10849-001-01 |
| Proprietary Name | Terapie Callus Remover |
| Package Description | 1 TUBE in 1 CARTON (10849-001-01) > 7.5 mL in 1 TUBE |
| Product NDC | 10849-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111104 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Armand Dupree |
| Substance Name | SALICYLIC ACID |
| Strength Number | 17 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
