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) |
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 NDC: | 10849-001-01 |
Package Description: | 1 TUBE in 1 CARTON (10849-001-01) > 7.5 mL in 1 TUBE |
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 |