| 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 |