| 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: | 29500-9085-5 |
| Package Description: | 710 mL in 1 BOTTLE (29500-9085-5) |
| NDC Code | 29500-9085-5 |
| Proprietary Name | Hand Sanitizer |
| Package Description | 710 mL in 1 BOTTLE (29500-9085-5) |
| 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 |