Product NDC: | 76138-001 |
Proprietary Name: | Antiseptic Hand Sanitizer |
Non Proprietary Name: | Alcohol |
Active Ingredient(s): | 36.58 mL/59mL & nbsp; Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76138-001 |
Labeler Name: | Innovation Specialties |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110327 |
Package NDC: | 76138-001-01 |
Package Description: | 59 mL in 1 BOTTLE (76138-001-01) |
NDC Code | 76138-001-01 |
Proprietary Name | Antiseptic Hand Sanitizer |
Package Description | 59 mL in 1 BOTTLE (76138-001-01) |
Product NDC | 76138-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110327 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Innovation Specialties |
Substance Name | ALCOHOL |
Strength Number | 36.58 |
Strength Unit | mL/59mL |
Pharmaceutical Classes |