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Handi-Sani
Handi-Sani - 76063-738-16 - (ALCOHOL)
Drug Information of Handi-Sani
| Product NDC: | 76063-738 |
| Proprietary Name: | Handi-Sani |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Handi-Sani
| Product NDC: | 76063-738 |
| Labeler Name: | Chromate Industrial Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110201 |
Package Information of Handi-Sani
| Package NDC: | 76063-738-16 |
| Package Description: | 236 mL in 1 BOTTLE, PLASTIC (76063-738-16) |
NDC Information of Handi-Sani
| NDC Code | 76063-738-16 |
| Proprietary Name | Handi-Sani |
| Package Description | 236 mL in 1 BOTTLE, PLASTIC (76063-738-16) |
| Product NDC | 76063-738 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Chromate Industrial Corporation |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
