Product NDC: | 55443-0200 |
Proprietary Name: | VioNexus |
Non Proprietary Name: | Chloroxylenol |
Active Ingredient(s): | .085; 77.01 g/100mL; g/100mL & nbsp; Chloroxylenol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55443-0200 |
Labeler Name: | Metrex Research |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19920101 |
Package NDC: | 55443-0200-5 |
Package Description: | 48 BOTTLE, PLASTIC in 1 CASE (55443-0200-5) > 59 mL in 1 BOTTLE, PLASTIC (55443-0200-1) |
NDC Code | 55443-0200-5 |
Proprietary Name | VioNexus |
Package Description | 48 BOTTLE, PLASTIC in 1 CASE (55443-0200-5) > 59 mL in 1 BOTTLE, PLASTIC (55443-0200-1) |
Product NDC | 55443-0200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chloroxylenol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19920101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Metrex Research |
Substance Name | BENZALKONIUM CHLORIDE; ETHANOL |
Strength Number | .085; 77.01 |
Strength Unit | g/100mL; g/100mL |
Pharmaceutical Classes |