Product NDC: | 68604-231 |
Proprietary Name: | Hand Kleen Foaming Antibacterial Hand |
Non Proprietary Name: | Triclosan |
Active Ingredient(s): | .3 g/100mL & nbsp; Triclosan |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68604-231 |
Labeler Name: | Auto-Chlor System, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121217 |
Package NDC: | 68604-231-02 |
Package Description: | 4 BAG in 1 BOX (68604-231-02) > 1000 mL in 1 BAG (68604-231-01) |
NDC Code | 68604-231-02 |
Proprietary Name | Hand Kleen Foaming Antibacterial Hand |
Package Description | 4 BAG in 1 BOX (68604-231-02) > 1000 mL in 1 BAG (68604-231-01) |
Product NDC | 68604-231 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Triclosan |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20121217 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Auto-Chlor System, LLC |
Substance Name | TRICLOSAN |
Strength Number | .3 |
Strength Unit | g/100mL |
Pharmaceutical Classes |