| Product NDC: | 66010-515 |
| Proprietary Name: | American Continental Techlabs, LLC INSTANT HAND SANITIZER |
| Non Proprietary Name: | ethanol |
| Active Ingredient(s): | 600 mL/1000mL & nbsp; ethanol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66010-515 |
| Labeler Name: | American Continental Techlabs |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100321 |
| Package NDC: | 66010-515-88 |
| Package Description: | 237 mL in 1 BOTTLE (66010-515-88) |
| NDC Code | 66010-515-88 |
| Proprietary Name | American Continental Techlabs, LLC INSTANT HAND SANITIZER |
| Package Description | 237 mL in 1 BOTTLE (66010-515-88) |
| Product NDC | 66010-515 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ethanol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100321 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | American Continental Techlabs |
| Substance Name | ETHANOL |
| Strength Number | 600 |
| Strength Unit | mL/1000mL |
| Pharmaceutical Classes |