Product NDC: | 51811-363 |
Proprietary Name: | Antimicrobial Hand Sanitizer |
Non Proprietary Name: | Alcohol |
Active Ingredient(s): | 39.33 mL/59.14mL & nbsp; Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51811-363 |
Labeler Name: | Hanover Pen Corp dba HPC Global |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100913 |
Package NDC: | 51811-363-12 |
Package Description: | 59.14 mL in 1 BOTTLE, PLASTIC (51811-363-12) |
NDC Code | 51811-363-12 |
Proprietary Name | Antimicrobial Hand Sanitizer |
Package Description | 59.14 mL in 1 BOTTLE, PLASTIC (51811-363-12) |
Product NDC | 51811-363 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100913 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Hanover Pen Corp dba HPC Global |
Substance Name | ALCOHOL |
Strength Number | 39.33 |
Strength Unit | mL/59.14mL |
Pharmaceutical Classes |