Product NDC: | 49765-200 |
Proprietary Name: | DepHyze Antiseptic Foam Hand Sanitizer |
Non Proprietary Name: | BENZALKONIUM CHLORIDE |
Active Ingredient(s): | .1 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49765-200 |
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: | 20091230 |
Package NDC: | 49765-200-10 |
Package Description: | 50 mL in 1 BOTTLE (49765-200-10) |
NDC Code | 49765-200-10 |
Proprietary Name | DepHyze Antiseptic Foam Hand Sanitizer |
Package Description | 50 mL in 1 BOTTLE (49765-200-10) |
Product NDC | 49765-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20091230 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | MicroPure Solutions, LLC dba Tionicon |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .1 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |