Product NDC: | 51706-507 |
Proprietary Name: | Hand Sanitizer |
Non Proprietary Name: | Alcohol |
Active Ingredient(s): | 62 mL/100mL & nbsp; Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51706-507 |
Labeler Name: | Landy International |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121101 |
Package NDC: | 51706-507-01 |
Package Description: | 29 mL in 1 BOTTLE (51706-507-01) |
NDC Code | 51706-507-01 |
Proprietary Name | Hand Sanitizer |
Package Description | 29 mL in 1 BOTTLE (51706-507-01) |
Product NDC | 51706-507 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20121101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Landy International |
Substance Name | ALCOHOL |
Strength Number | 62 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |