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Hand Sanitizer
Hand Sanitizer - 17518-001-01 - (Ethyl Alcohol)
Drug Information of Hand Sanitizer
| Product NDC: | 17518-001 |
| Proprietary Name: | Hand Sanitizer |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | 62 g/100mL & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hand Sanitizer
| Product NDC: | 17518-001 |
| Labeler Name: | 3M Health Care |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120409 |
Package Information of Hand Sanitizer
| Package NDC: | 17518-001-01 |
| Package Description: | 44 mL in 1 BOTTLE, PLASTIC (17518-001-01) |
NDC Information of Hand Sanitizer
| NDC Code | 17518-001-01 |
| Proprietary Name | Hand Sanitizer |
| Package Description | 44 mL in 1 BOTTLE, PLASTIC (17518-001-01) |
| Product NDC | 17518-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120409 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | 3M Health Care |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
