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: | 26550-001-12 |
Package Description: | 75 mL in 1 BOTTLE (26550-001-12) |
NDC Code | 26550-001-12 |
Proprietary Name | X3 Clean |
Package Description | 75 mL in 1 BOTTLE (26550-001-12) |
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 |