Home > National Drug Code (NDC) > Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22

Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22 - 62839-3904-1 - (Avobenzone, Homosalate, Octisalate, and Octocrylene)

Alphabetical Index


Drug Information of Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22

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)

Labeler Information of Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22

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 Information of Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22

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 Information of Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22

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

Complete Information of Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22


General Information