Product NDC: | 52559-575 |
Proprietary Name: | Anchor Foaming Hand Sanitizer |
Non Proprietary Name: | BENZETHONIUM CHLORIDE |
Active Ingredient(s): | 2 mg/mL & nbsp; BENZETHONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52559-575 |
Labeler Name: | Anchor Supply Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 52559-575-10 |
Package Description: | 1000 mL in 1 CARTRIDGE (52559-575-10) |
NDC Code | 52559-575-10 |
Proprietary Name | Anchor Foaming Hand Sanitizer |
Package Description | 1000 mL in 1 CARTRIDGE (52559-575-10) |
Product NDC | 52559-575 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZETHONIUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Anchor Supply Company |
Substance Name | BENZETHONIUM CHLORIDE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes |