Product NDC: | 51143-541 |
Proprietary Name: | Antibacterial Liquid Hand |
Non Proprietary Name: | TRICLOSAN |
Active Ingredient(s): | .115 kg/100L & nbsp; TRICLOSAN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51143-541 |
Labeler Name: | OnPoint, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090730 |
Package NDC: | 51143-541-96 |
Package Description: | .221 L in 1 BOTTLE, PLASTIC (51143-541-96) |
NDC Code | 51143-541-96 |
Proprietary Name | Antibacterial Liquid Hand |
Package Description | .221 L in 1 BOTTLE, PLASTIC (51143-541-96) |
Product NDC | 51143-541 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TRICLOSAN |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20090730 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | OnPoint, Inc |
Substance Name | TRICLOSAN |
Strength Number | .115 |
Strength Unit | kg/100L |
Pharmaceutical Classes |