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 |