Product NDC: | 65055-701 |
Proprietary Name: | Antibacterial Hand Sanitizer |
Non Proprietary Name: | ETHYL ALCOHOL |
Active Ingredient(s): | 64 g/100mL & nbsp; ETHYL ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65055-701 |
Labeler Name: | Laboratorios Jaloma, S.A. de C.V. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091101 |
Package NDC: | 65055-701-01 |
Package Description: | 120 mL in 1 BOTTLE, PLASTIC (65055-701-01) |
NDC Code | 65055-701-01 |
Proprietary Name | Antibacterial Hand Sanitizer |
Package Description | 120 mL in 1 BOTTLE, PLASTIC (65055-701-01) |
Product NDC | 65055-701 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ETHYL ALCOHOL |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20091101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Laboratorios Jaloma, S.A. de C.V. |
Substance Name | ALCOHOL |
Strength Number | 64 |
Strength Unit | g/100mL |
Pharmaceutical Classes |