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Handi-San
Handi-San - 62712-575-27 - (BENZETHONIUM CHLORIDE)
Drug Information of Handi-San
| Product NDC: | 62712-575 |
| Proprietary Name: | Handi-San |
| Non Proprietary Name: | BENZETHONIUM CHLORIDE |
| Active Ingredient(s): | 2 mg/mL & nbsp; BENZETHONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Handi-San
| Product NDC: | 62712-575 |
| Labeler Name: | Atco International |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20060101 |
Package Information of Handi-San
| Package NDC: | 62712-575-27 |
| Package Description: | 800 mL in 1 CARTRIDGE (62712-575-27) |
NDC Information of Handi-San
| NDC Code | 62712-575-27 |
| Proprietary Name | Handi-San |
| Package Description | 800 mL in 1 CARTRIDGE (62712-575-27) |
| Product NDC | 62712-575 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZETHONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20060101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Atco International |
| Substance Name | BENZETHONIUM CHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
