Product NDC: | 63779-514 |
Proprietary Name: | HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer |
Non Proprietary Name: | Husky 514 |
Active Ingredient(s): | 1 g/1000mL & nbsp; Husky 514 |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63779-514 |
Labeler Name: | Canberra Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091116 |
Package NDC: | 63779-514-99 |
Package Description: | 250 mL in 1 BOTTLE (63779-514-99) |
NDC Code | 63779-514-99 |
Proprietary Name | HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer |
Package Description | 250 mL in 1 BOTTLE (63779-514-99) |
Product NDC | 63779-514 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Husky 514 |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20091116 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Canberra Corporation |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | 1 |
Strength Unit | g/1000mL |
Pharmaceutical Classes |