Home
>
National Drug Code (NDC)
>
DermaFoam E
DermaFoam E - 63146-103-41 - (Antiseptic handwash)
Drug Information of DermaFoam E
| Product NDC: | 63146-103 |
| Proprietary Name: | DermaFoam E |
| Non Proprietary Name: | Antiseptic handwash |
| Active Ingredient(s): | 1 mL/100mL & nbsp; Antiseptic handwash |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DermaFoam E
| Product NDC: | 63146-103 |
| Labeler Name: | Kay Chemical |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20051013 |
Package Information of DermaFoam E
| Package NDC: | 63146-103-41 |
| Package Description: | 750 mL in 1 BOTTLE, PLASTIC (63146-103-41) |
NDC Information of DermaFoam E
| NDC Code | 63146-103-41 |
| Proprietary Name | DermaFoam E |
| Package Description | 750 mL in 1 BOTTLE, PLASTIC (63146-103-41) |
| Product NDC | 63146-103 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Antiseptic handwash |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20051013 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kay Chemical |
| Substance Name | CHLOROXYLENOL |
| Strength Number | 1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
