| Product NDC: | 49765-100 |
| Proprietary Name: | DepHyze Antiseptic Foam Hand Sanitizer |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .13 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49765-100 |
| Labeler Name: | MicroPure Solutions, LLC dba Tionicon |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091101 |
| Package NDC: | 49765-100-10 |
| Package Description: | 50 mL in 1 BOTTLE (49765-100-10) |
| NDC Code | 49765-100-10 |
| Proprietary Name | DepHyze Antiseptic Foam Hand Sanitizer |
| Package Description | 50 mL in 1 BOTTLE (49765-100-10) |
| Product NDC | 49765-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MicroPure Solutions, LLC dba Tionicon |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .13 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |