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Hand Sanitizer
Hand Sanitizer - 61734-102-01 - (Benzethonium)
Drug Information of Hand Sanitizer
| Product NDC: | 61734-102 |
| Proprietary Name: | Hand Sanitizer |
| Non Proprietary Name: | Benzethonium |
| Active Ingredient(s): | .2 mg/100mL & nbsp; Benzethonium |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hand Sanitizer
| Product NDC: | 61734-102 |
| Labeler Name: | Delon Laboratories (1990) Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100520 |
Package Information of Hand Sanitizer
| Package NDC: | 61734-102-01 |
| Package Description: | 7 mL in 1 BOTTLE, SPRAY (61734-102-01) |
NDC Information of Hand Sanitizer
| NDC Code | 61734-102-01 |
| Proprietary Name | Hand Sanitizer |
| Package Description | 7 mL in 1 BOTTLE, SPRAY (61734-102-01) |
| Product NDC | 61734-102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzethonium |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100520 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Delon Laboratories (1990) Ltd |
| Substance Name | BENZETHONIUM CHLORIDE |
| Strength Number | .2 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
