| Product NDC: | 50730-8608 |
| Proprietary Name: | Antiseptic Hand Gel |
| Non Proprietary Name: | ethyl alcohol |
| Active Ingredient(s): | .7 mL/mL & nbsp; ethyl alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50730-8608 |
| Labeler Name: | H and P Industries, Inc. dba Triad Group |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19971117 |
| Package NDC: | 50730-8608-4 |
| Package Description: | 236 mL in 1 BOTTLE, PLASTIC (50730-8608-4) |
| NDC Code | 50730-8608-4 |
| Proprietary Name | Antiseptic Hand Gel |
| Package Description | 236 mL in 1 BOTTLE, PLASTIC (50730-8608-4) |
| Product NDC | 50730-8608 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ethyl alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19971117 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H and P Industries, Inc. dba Triad Group |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |