Product NDC: | 11084-017 |
Proprietary Name: | InstantFOAM alcohol hand sanitizer |
Non Proprietary Name: | Ethyl Alcohol |
Active Ingredient(s): | 72 mL/100mL & nbsp; Ethyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11084-017 |
Labeler Name: | Deb USA, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20080602 |
Package NDC: | 11084-017-01 |
Package Description: | 47 mL in 1 BOTTLE, PUMP (11084-017-01) |
NDC Code | 11084-017-01 |
Proprietary Name | InstantFOAM alcohol hand sanitizer |
Package Description | 47 mL in 1 BOTTLE, PUMP (11084-017-01) |
Product NDC | 11084-017 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethyl Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20080602 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Deb USA, Inc. |
Substance Name | ALCOHOL |
Strength Number | 72 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |