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Byotrol Antibacterial Foaming Hand Sanitizer
Byotrol Antibacterial Foaming Hand Sanitizer - 42719-346-50 - (BENZALKONIUM CHLORIDE)
Drug Information of Byotrol Antibacterial Foaming Hand Sanitizer
| Product NDC: | 42719-346 |
| Proprietary Name: | Byotrol Antibacterial Foaming Hand Sanitizer |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | 1.3 mg/mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Byotrol Antibacterial Foaming Hand Sanitizer
| Product NDC: | 42719-346 |
| Labeler Name: | Byotrol, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130308 |
Package Information of Byotrol Antibacterial Foaming Hand Sanitizer
| Package NDC: | 42719-346-50 |
| Package Description: | 500 mL in 1 BOTTLE (42719-346-50) |
NDC Information of Byotrol Antibacterial Foaming Hand Sanitizer
| NDC Code | 42719-346-50 |
| Proprietary Name | Byotrol Antibacterial Foaming Hand Sanitizer |
| Package Description | 500 mL in 1 BOTTLE (42719-346-50) |
| Product NDC | 42719-346 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130308 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Byotrol, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
