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TRICLOSAN
TRICLOSAN - 59779-081-20 - (TRICLOSAN)
Drug Information of TRICLOSAN
| Product NDC: | 59779-081 |
| Proprietary Name: | TRICLOSAN |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | 29 mg/mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRICLOSAN
| Product NDC: | 59779-081 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080601 |
Package Information of TRICLOSAN
| Package NDC: | 59779-081-20 |
| Package Description: | 240 mL in 1 BOTTLE (59779-081-20) |
NDC Information of TRICLOSAN
| NDC Code | 59779-081-20 |
| Proprietary Name | TRICLOSAN |
| Package Description | 240 mL in 1 BOTTLE (59779-081-20) |
| Product NDC | 59779-081 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20080601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | TRICLOSAN |
| Strength Number | 29 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
