NU SKIN AGELOC RADIANT DAY BROAD SPECTRUM SPF 22- avobenzone, homosalate, octisalate, and octocrylene lotion 
NSE Products, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Nu Skin® ageLOC® Radiant Day Broad Spectrum SPF 22

Drug Facts

Active Ingredient

Avobenzone (3%), Homosalate (5%), Octisalate (4%), Octocrylene (2%)

Purpose

Sunscreen

Use

Warnings

  • For external use only.
     
  • Do not use on damaged or broken skin

  • Stop use and ask a doctor if rash occurs

  • When using this product, keep out of eyes. Rinse with water to remove.

  • Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive Ingredients

Water (Aqua), Glycerin, Cetyl Dimethicone, Cyclopentasiloxane, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Caprylyl Glycol, Glyceryl Stearate, PEG-100 Stearate, Dimethicone, Cyclohexasiloxane, Dimethicone/ Vinyl Dimethicone Crosspolymer, Cetyl Alcohol, Methyl Gluceth-10, Steareth-2, Steareth-21, Isohexadecane, Nylon-12, Hydrolyzed Jojoba Esters, Jojoba Esters, Bambusa Vulgaris Leaf/Stem Extract, Glucosamine HCl, Pisum Sativum (Pea) Extract, Hexapeptide-2, Narcissus Tazetta Bulb Extract, Schizandra Chinensis Fruit Extract, Butyrospermum Parkii (Shea Butter), Polysorbate 80, Titanium Dioxide, Butylene Glycol, Citric Acid, Disodium EDTA, Fragrance (Parfum), Chlorphenesin, Phenoxyethanol.

Other Information

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 25 ml Tube Carton

ageLOC® RADIANT DAY
BROAD SPECTRUM SPF 22

NU SKIN®

25 ml e (0.85 fl .oz.)

PRINCIPAL DISPLAY PANEL - 25 ml Tube Carton
NU SKIN AGELOC RADIANT DAY BROAD SPECTRUM SPF 22 
avobenzone, homosalate, octisalate, and octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-3904
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone30 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate50 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate40 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
METHYL GLUCETH-10 (UNII: N0MWT4C7WH)  
STEARETH-2 (UNII: V56DFE46J5)  
STEARETH-21 (UNII: 53J3F32P58)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
NYLON-12 (UNII: 446U8J075B)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)  
SHEA BUTTER (UNII: K49155WL9Y)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
PEA (UNII: W4X7H8GYFM)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)  
NARCISSUS TAZETTA BULB (UNII: K17762966S)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62839-3904-11 in 1 CARTON05/01/2013
125 mL in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35205/01/2013
Labeler - NSE Products, Inc. (803486393)

Revised: 1/2022
Document Id: 3cc7123b-dc30-47d9-97a4-96eb30f8cda7
Set id: 649a9c28-bfd4-404c-90d5-5d0ea8c7b645
Version: 3
Effective Time: 20220111
 
NSE Products, Inc.