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Stay Clean Foam Hand Sanitizer
Stay Clean Foam Hand Sanitizer - 42719-345-51 - (Hand Sanitizer)
Drug Information of Stay Clean Foam Hand Sanitizer
| Product NDC: | 42719-345 |
| Proprietary Name: | Stay Clean Foam Hand Sanitizer |
| Non Proprietary Name: | Hand Sanitizer |
| Active Ingredient(s): | .13 mL/100mL & nbsp; Hand Sanitizer |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stay Clean Foam Hand Sanitizer
| Product NDC: | 42719-345 |
| Labeler Name: | Byotrol, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090918 |
Package Information of Stay Clean Foam Hand Sanitizer
| Package NDC: | 42719-345-51 |
| Package Description: | 210 mL in 1 BOTTLE (42719-345-51) |
NDC Information of Stay Clean Foam Hand Sanitizer
| NDC Code | 42719-345-51 |
| Proprietary Name | Stay Clean Foam Hand Sanitizer |
| Package Description | 210 mL in 1 BOTTLE (42719-345-51) |
| Product NDC | 42719-345 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hand Sanitizer |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20090918 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Byotrol, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .13 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
