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TRICLOSAN
TRICLOSAN - 21749-415-20 - (TRICLOSAN)
Drug Information of TRICLOSAN
| Product NDC: | 21749-415 |
| Proprietary Name: | TRICLOSAN |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .003 mL/mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRICLOSAN
| Product NDC: | 21749-415 |
| Labeler Name: | GOJO Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100310 |
Package Information of TRICLOSAN
| Package NDC: | 21749-415-20 |
| Package Description: | 2000 mL in 1 BOX (21749-415-20) |
NDC Information of TRICLOSAN
| NDC Code | 21749-415-20 |
| Proprietary Name | TRICLOSAN |
| Package Description | 2000 mL in 1 BOX (21749-415-20) |
| Product NDC | 21749-415 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100310 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GOJO Industries, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | .003 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
