Product NDC: | 64024-100 |
Proprietary Name: | Source Antibacterial Foaming Hand Original |
Non Proprietary Name: | Triclosan |
Active Ingredient(s): | .46 mg/mL & nbsp; Triclosan |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64024-100 |
Labeler Name: | Aldi Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130104 |
Package NDC: | 64024-100-01 |
Package Description: | 222 mL in 1 BOTTLE (64024-100-01) |
NDC Code | 64024-100-01 |
Proprietary Name | Source Antibacterial Foaming Hand Original |
Package Description | 222 mL in 1 BOTTLE (64024-100-01) |
Product NDC | 64024-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Triclosan |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130104 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Aldi Inc. |
Substance Name | TRICLOSAN |
Strength Number | .46 |
Strength Unit | mg/mL |
Pharmaceutical Classes |