Product NDC: | 11673-264 |
Proprietary Name: | PREMIUM HAND SANITIZER |
Non Proprietary Name: | ETHYL ALCOHOL |
Active Ingredient(s): | 62 mL/100mL & nbsp; ETHYL ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11673-264 |
Labeler Name: | TARGET |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110321 |
Package NDC: | 11673-264-02 |
Package Description: | 59.1 mL in 1 BOTTLE (11673-264-02) |
NDC Code | 11673-264-02 |
Proprietary Name | PREMIUM HAND SANITIZER |
Package Description | 59.1 mL in 1 BOTTLE (11673-264-02) |
Product NDC | 11673-264 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ETHYL ALCOHOL |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110321 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | TARGET |
Substance Name | ALCOHOL |
Strength Number | 62 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |