Product NDC: | 29500-9085 |
Proprietary Name: | Hand Sanitizer |
Non Proprietary Name: | ethyl alcohol |
Active Ingredient(s): | 9.3 mL/60mL & nbsp; ethyl alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 29500-9085 |
Labeler Name: | Personal Care Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120120 |
Package NDC: | 29500-9085-3 |
Package Description: | 355 mL in 1 BOTTLE (29500-9085-3) |
NDC Code | 29500-9085-3 |
Proprietary Name | Hand Sanitizer |
Package Description | 355 mL in 1 BOTTLE (29500-9085-3) |
Product NDC | 29500-9085 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ethyl alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20120120 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Personal Care Products |
Substance Name | ALCOHOL |
Strength Number | 9.3 |
Strength Unit | mL/60mL |
Pharmaceutical Classes |