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 |