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Nu Skin Nu Colour
Nu Skin Nu Colour - 62839-0820-1 - (Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide)
Drug Information of Nu Skin Nu Colour
| Product NDC: | 62839-0820 |
| Proprietary Name: | Nu Skin Nu Colour |
| Non Proprietary Name: | Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide |
| Active Ingredient(s): | 50; 20; 30; 65.22 g/1000mL; g/1000mL; g/1000mL; g/1000mL & nbsp; Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nu Skin Nu Colour
| Product NDC: | 62839-0820 |
| Labeler Name: | NSE Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110103 |
Package Information of Nu Skin Nu Colour
| Package NDC: | 62839-0820-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (62839-0820-1) > 30 mL in 1 BOTTLE, PUMP |
NDC Information of Nu Skin Nu Colour
| NDC Code | 62839-0820-1 |
| Proprietary Name | Nu Skin Nu Colour |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (62839-0820-1) > 30 mL in 1 BOTTLE, PUMP |
| Product NDC | 62839-0820 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110103 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NSE Products, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 50; 20; 30; 65.22 |
| Strength Unit | g/1000mL; g/1000mL; g/1000mL; g/1000mL |
| Pharmaceutical Classes |
