Product NDC: | 31190-100 |
Proprietary Name: | ALCOHOL FREE HAND SANITIZER |
Non Proprietary Name: | BENZALKONIUM CHLORIDE |
Active Ingredient(s): | .13 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 31190-100 |
Labeler Name: | Shanghai Kejing Cleaning Products Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100407 |
Package NDC: | 31190-100-60 |
Package Description: | 60 mL in 1 PACKAGE (31190-100-60) |
NDC Code | 31190-100-60 |
Proprietary Name | ALCOHOL FREE HAND SANITIZER |
Package Description | 60 mL in 1 PACKAGE (31190-100-60) |
Product NDC | 31190-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20100407 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Shanghai Kejing Cleaning Products Co., Ltd. |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .13 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |