Product NDC: | 62654-141 |
Proprietary Name: | DermaCen Non-Alcohol Foaming Hand Sanitizer |
Non Proprietary Name: | Benzalkonium Chloride |
Active Ingredient(s): | .13 mL/100mL & nbsp; Benzalkonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62654-141 |
Labeler Name: | Central Solutions Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100118 |
Package NDC: | 62654-141-16 |
Package Description: | 1000 mL in 1 BOTTLE, PUMP (62654-141-16) |
NDC Code | 62654-141-16 |
Proprietary Name | DermaCen Non-Alcohol Foaming Hand Sanitizer |
Package Description | 1000 mL in 1 BOTTLE, PUMP (62654-141-16) |
Product NDC | 62654-141 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100118 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Central Solutions Inc |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .13 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |