Product NDC: | 76116-100 |
Proprietary Name: | first depHense Alcohol-Free Antiseptic Foam 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: | 76116-100 |
Labeler Name: | First Dephense, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110113 |
Package NDC: | 76116-100-01 |
Package Description: | 50 mL in 1 BOTTLE, PUMP (76116-100-01) |
NDC Code | 76116-100-01 |
Proprietary Name | first depHense Alcohol-Free Antiseptic Foam Hand Sanitizer |
Package Description | 50 mL in 1 BOTTLE, PUMP (76116-100-01) |
Product NDC | 76116-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110113 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | First Dephense, LLC |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .13 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |