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Clearskin
Clearskin - 10096-0199-1 - (TRICLOSAN)
Drug Information of Clearskin
| Product NDC: | 10096-0199 |
| Proprietary Name: | Clearskin |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .5 mL/125mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clearskin
| Product NDC: | 10096-0199 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100602 |
Package Information of Clearskin
| Package NDC: | 10096-0199-1 |
| Package Description: | 125 mL in 1 TUBE (10096-0199-1) |
NDC Information of Clearskin
| NDC Code | 10096-0199-1 |
| Proprietary Name | Clearskin |
| Package Description | 125 mL in 1 TUBE (10096-0199-1) |
| Product NDC | 10096-0199 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100602 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | .5 |
| Strength Unit | mL/125mL |
| Pharmaceutical Classes |
