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Nu Skin
Nu Skin - 62839-0271-9 - (Triclosan)
Drug Information of Nu Skin
| Product NDC: | 62839-0271 |
| Proprietary Name: | Nu Skin |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .55 mL/100mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nu Skin
| Product NDC: | 62839-0271 |
| Labeler Name: | NSE Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19960826 |
Package Information of Nu Skin
| Package NDC: | 62839-0271-9 |
| Package Description: | 500 mL in 1 BOTTLE, PLASTIC (62839-0271-9) |
NDC Information of Nu Skin
| NDC Code | 62839-0271-9 |
| Proprietary Name | Nu Skin |
| Package Description | 500 mL in 1 BOTTLE, PLASTIC (62839-0271-9) |
| Product NDC | 62839-0271 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19960826 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NSE Products, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | .55 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
