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Anti-Bacterial Gentle Foaming Hand
Anti-Bacterial Gentle Foaming Hand - 62670-4519-3 - (Triclosan)
Drug Information of Anti-Bacterial Gentle Foaming Hand
| Product NDC: | 62670-4519 |
| Proprietary Name: | Anti-Bacterial Gentle Foaming Hand |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | 3 mg/g & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti-Bacterial Gentle Foaming Hand
| Product NDC: | 62670-4519 |
| Labeler Name: | Bath & Body Works, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130423 |
Package Information of Anti-Bacterial Gentle Foaming Hand
| Package NDC: | 62670-4519-3 |
| Package Description: | 263 g in 1 PACKAGE (62670-4519-3) |
NDC Information of Anti-Bacterial Gentle Foaming Hand
| NDC Code | 62670-4519-3 |
| Proprietary Name | Anti-Bacterial Gentle Foaming Hand |
| Package Description | 263 g in 1 PACKAGE (62670-4519-3) |
| Product NDC | 62670-4519 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20130423 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bath & Body Works, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | 3 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
