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Hand Sanitizer
Hand Sanitizer - 61734-085-09 - (Ethyl Alcohol)
Drug Information of Hand Sanitizer
| Product NDC: | 61734-085 |
| Proprietary Name: | Hand Sanitizer |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | 62 mg/117.6mL & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hand Sanitizer
| Product NDC: | 61734-085 |
| Labeler Name: | Delon Laboratories (1990) Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101001 |
Package Information of Hand Sanitizer
| Package NDC: | 61734-085-09 |
| Package Description: | 725 mL in 1 BOTTLE, PLASTIC (61734-085-09) |
NDC Information of Hand Sanitizer
| NDC Code | 61734-085-09 |
| Proprietary Name | Hand Sanitizer |
| Package Description | 725 mL in 1 BOTTLE, PLASTIC (61734-085-09) |
| Product NDC | 61734-085 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20101001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Delon Laboratories (1990) Ltd |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mg/117.6mL |
| Pharmaceutical Classes |
