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DERMAPROT
DERMAPROT - 66854-004-01 - (TRICLOSAN)
Drug Information of DERMAPROT
| Product NDC: | 66854-004 |
| Proprietary Name: | DERMAPROT |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .3 mg/100mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DERMAPROT
| Product NDC: | 66854-004 |
| Labeler Name: | SAPI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120830 |
Package Information of DERMAPROT
| Package NDC: | 66854-004-01 |
| Package Description: | 500 mL in 1 BOTTLE (66854-004-01) |
NDC Information of DERMAPROT
| NDC Code | 66854-004-01 |
| Proprietary Name | DERMAPROT |
| Package Description | 500 mL in 1 BOTTLE (66854-004-01) |
| Product NDC | 66854-004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120830 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SAPI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Substance Name | TRICLOSAN |
| Strength Number | .3 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
