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Protex - 35000-850-19 - (Triclocarban)
Drug Information of Protex
| Product NDC: | 35000-850 |
| Proprietary Name: | Protex |
| Non Proprietary Name: | Triclocarban |
| Active Ingredient(s): | 1.5 mg/1000mL & nbsp; Triclocarban |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Protex
| Product NDC: | 35000-850 |
| Labeler Name: | Colgate-Palmolive Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110610 |
Package Information of Protex
| Package NDC: | 35000-850-19 |
| Package Description: | 590 mL in 1 BOTTLE (35000-850-19) |
NDC Information of Protex
| NDC Code | 35000-850-19 |
| Proprietary Name | Protex |
| Package Description | 590 mL in 1 BOTTLE (35000-850-19) |
| Product NDC | 35000-850 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclocarban |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110610 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Colgate-Palmolive Company |
| Substance Name | TRICLOCARBAN |
| Strength Number | 1.5 |
| Strength Unit | mg/1000mL |
| Pharmaceutical Classes |
