ARTISTRY IDEAL RADIANCE UV PROTECT SPF 50 PLUS BROAD SPECTRUM SUNSCREEN- octinoxate, octisalate, zinc oxide, titanium dioxide cream 
Amway Corp

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ARTISTRY IDEAL RADIANCE UV Protect SPF 50+ Broad Spectrum Sunscreen

ARTISTRY IDEAL RADIANCE UV Protect SPF 50+ Broad Spectrum Sunscreen

Active Ingredients

Octinoxate 6.8% (W/W P/P) Octisalate 4.5% (W/W P/P) Zinc Oxide 12.66% (W/W P/P) Titanium Dioxide 2.49% (W/W P/P)


Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

For external use only

Do not use

on broken or damaged skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash occurs

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Other information

Protect this product from excessive heat and direct sun

Inactive ingredients

WATER/AQUA, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, ALCOHOL, DICAPRYLYL CARBONATE, DIMETHICONE, PEG-10 DIMETHICONE, MAGNESIUM SULFATE, METHYL METHACRYLATE CROSSPOLYMER, VINYL DIMETHICONE/ METHICONE SILSESQUIOXANE CROSSPOLYMER, ALUMINUM HYDROXIDE, TRIETHOXYCAPRYLYLSILANE, ALUMINUM STEARATE, FRAGRANCE / PARFUM, CAPRYLYL GLYCOL, PHENOXYETHANOL, POLYGLYCERYL-6 POLYRICINOLEATE, GLYCERYL CAPRYLATE, BELLIS PERENNIS (DAISY) FLOWER EXTRACT, MALTODEXTRIN, SODIUM HYALURONATE, GLYCERIN, JASMINUM OFFICINALE(JASMINE) FLOWER EXTRACT, LECITHIN, HYDROLYZED CONCHIOLIN PROTEIN, SOPHORA JAPONICA LEAF EXTRACT, GERANIUM ROBERTIANUM EXTRACT, LACTOBACILLUS/ACEROLA CHERRY FERMENT, OENOTHERA BIENNIS (EVENING PRIMROSE) SEED EXTRACT, GLYCERIN, BETA-SITOSTEROL, CERAMIDE 3, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, TETRAHEXYLDECYL ASCORBATE, TOCOPHERYL ACETATE.

Directions

For sunscreen use

To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:

Package Labeling:

Label7

ARTISTRY IDEAL RADIANCE UV PROTECT SPF 50 PLUS BROAD SPECTRUM SUNSCREEN 
octinoxate, octisalate, zinc oxide, titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50390-108
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE68 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE45 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE126.6 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE24.9 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ALCOHOL (UNII: 3K9958V90M)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
METHYL METHACRYLATE (UNII: 196OC77688)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ALUMINUM STEARATE (UNII: U6XF9NP8HM)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)  
BELLIS PERENNIS (UNII: 2HU33I03UY)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
GLYCERIN (UNII: PDC6A3C0OX)  
JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)  
STYPHNOLOBIUM JAPONICUM LEAF (UNII: E63W4N1K61)  
GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL)  
ACEROLA (UNII: XDD2WEC9L5)  
OENOTHERA BIENNIS SEED (UNII: 634OA3ULTM)  
.BETA.-SITOSTEROL (UNII: S347WMO6M4)  
CERAMIDE 3 (UNII: 4370DF050B)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50390-108-301 in 1 CARTON09/11/2013
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/11/2013
Labeler - Amway Corp (083416854)

Revised: 1/2024
Document Id: 0daad476-bd32-bd5d-e063-6394a90ac74a
Set id: a1a700b5-d039-4bd2-8420-5c2053095706
Version: 7
Effective Time: 20240102
 
Amway Corp