| Product NDC: | 62839-3904 |
| Proprietary Name: | Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22 |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Active Ingredient(s): | 30; 50; 40; 20 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62839-3904 |
| Labeler Name: | NSE Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130501 |
| Package NDC: | 62839-3904-1 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (62839-3904-1) > 25 mL in 1 TUBE, WITH APPLICATOR |
| NDC Code | 62839-3904-1 |
| Proprietary Name | Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22 |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (62839-3904-1) > 25 mL in 1 TUBE, WITH APPLICATOR |
| Product NDC | 62839-3904 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NSE Products, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 30; 50; 40; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |