| Product NDC: | 26550-001 |
| Proprietary Name: | X3 Clean |
| Non Proprietary Name: | Hand Sanitizer Foam |
| Active Ingredient(s): | 1.3 uL/mL & nbsp; Hand Sanitizer Foam |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 26550-001 |
| Labeler Name: | X3 Labs Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090901 |
| Package NDC: | 26550-001-14 |
| Package Description: | 250 mL in 1 BOTTLE (26550-001-14) |
| NDC Code | 26550-001-14 |
| Proprietary Name | X3 Clean |
| Package Description | 250 mL in 1 BOTTLE (26550-001-14) |
| Product NDC | 26550-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hand Sanitizer Foam |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | X3 Labs Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | uL/mL |
| Pharmaceutical Classes |