Product NDC: | 60193-201 |
Proprietary Name: | Woodwards HandClens Foaming Sanitizer |
Non Proprietary Name: | BENZALKONIUM CHLORIDE |
Active Ingredient(s): | 1.3 mg/mL & nbsp; BENZALKONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60193-201 |
Labeler Name: | Pacific Word Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130603 |
Package NDC: | 60193-201-05 |
Package Description: | 1800 mL in 1 BOTTLE, PUMP (60193-201-05) |
NDC Code | 60193-201-05 |
Proprietary Name | Woodwards HandClens Foaming Sanitizer |
Package Description | 1800 mL in 1 BOTTLE, PUMP (60193-201-05) |
Product NDC | 60193-201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130603 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Pacific Word Corporation |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | 1.3 |
Strength Unit | mg/mL |
Pharmaceutical Classes |