Product NDC: | 50260-500 |
Proprietary Name: | NON ALCOHOL HAND SANITIZER |
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: | 50260-500 |
Labeler Name: | Fercy Personal Care Products Co Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101113 |
Package NDC: | 50260-500-03 |
Package Description: | 8 mL in 1 BOTTLE, PLASTIC (50260-500-03) |
NDC Code | 50260-500-03 |
Proprietary Name | NON ALCOHOL HAND SANITIZER |
Package Description | 8 mL in 1 BOTTLE, PLASTIC (50260-500-03) |
Product NDC | 50260-500 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20101113 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Fercy Personal Care Products Co Limited |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .1 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |