Product NDC: | 76273-001 |
Proprietary Name: | Antibacterial Hand |
Non Proprietary Name: | BENZALKONIUM CHLORIDE |
Active Ingredient(s): | .1 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76273-001 |
Labeler Name: | MAYBORN USA, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110727 |
Package NDC: | 76273-001-01 |
Package Description: | 50 mL in 1 BOTTLE, PLASTIC (76273-001-01) |
NDC Code | 76273-001-01 |
Proprietary Name | Antibacterial Hand |
Package Description | 50 mL in 1 BOTTLE, PLASTIC (76273-001-01) |
Product NDC | 76273-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110727 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | MAYBORN USA, INC. |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .1 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |