ARTISTRY BEAUTY BALM PERFECTING PRIMER SPF 35 BROAD SPECTRUM SUNSCREEN- ensulizole, octinoxate, zinc oxide cream 
Amway Corp

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Artistry Beauty Balm Perfecting Primer SPF 35 Broad Spectrum Sunscreen Cream

Active Ingredients

Ensulizole 2.0% (W/W P/P) Octinoxate 5.0% (W/W P/P) Zinc Oxide 5.49% (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.

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/EAU, DIMETHICONE, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, GLYCERIN, TALC, METHYL TRIMETHICONE, TRIMETHYLOLPROPANE TRICAPRYLATE/ TRICAPRATE, LAURYL PEG-9, POLYDIMETHYLSILOXYETHYL DIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, DIMETHICONE/PEG-10/15 CROSSPOLYMER, TRIETHANOLAMINE, POLYGLYCERYL-6 POLYRICINOLEATE, POLYSILICONE-11, LECITHIN, PHENOXYETHANOL, SODIUM CHLORIDE, SODIUM CITRATE, POLYMETHYL METHACRYLATE, ALUMINA, POLYSORBATE-20, PEG/ PPG-18/18 DIMETHICONE, TRISILOXANE, HYDROGEN DIMETHICONE, METHYLPARABEN, DISODIUM EDTA, SILICA, PROPYLPARABEN, TRIETHOXYCAPRYLYLSILANE, ETHYLPARABEN, LAURETH-12, METHYLDIHYDROJASMONATE, IODOPROPYNYL BUTYLCARBAMATE, PEARL POWDER,ETHYLENE BRASSYLATE, ETHYL 2,2-DIMETHYLHYDROCINNAMAL, YEAST EXTRACT, CERAMIDE 3, BETA-SITOSTEROL, SODIUM HYALURONATE, GLUCOSAMINE HCL, UREA, ALGAE EXTRACT, TOCOPHEROL. MAY CONTAIN/PEUT CONTEINIR: IRON OXIDES (CI 77491, 77492, 77499), MICA (CI 77019), TITANIUM DIOXIDE (CI 77891).

Directions

For suncreen use

Package Labeling

carton

ARTISTRY BEAUTY BALM PERFECTING PRIMER SPF 35 BROAD SPECTRUM SUNSCREEN 
ensulizole, octinoxate, zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50390-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE20 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION54.9 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GLYCERIN (UNII: PDC6A3C0OX)  
TALC (UNII: 7SEV7J4R1U)  
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE (UNII: N1TRQ06KVJ)  
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)  
DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
TROLAMINE (UNII: 9O3K93S3TK)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
LAURETH-12 (UNII: OAH19558U1)  
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
PEARL (HYRIOPSIS CUMINGII) (UNII: A75L5FZ40U)  
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
ETHYL 2,2-DIMETHYLHYDROCINNAMAL (UNII: 5V2FN5AA3W)  
YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)  
CERAMIDE 3 (UNII: 4370DF050B)  
.BETA.-SITOSTEROL (UNII: S347WMO6M4)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)  
UREA (UNII: 8W8T17847W)  
TOCOPHEROL (UNII: R0ZB2556P8)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
MICA (UNII: V8A1AW0880)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50390-004-3030 mL in 1 TUBE; Type 0: Not a Combination Product05/05/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02005/05/2015
Labeler - Amway Corp (083416854)
Establishment
NameAddressID/FEIBusiness Operations
Access Business Group LLC839830713manufacture(50390-004)

Revised: 10/2023
Document Id: 0837939a-f051-8ac1-e063-6294a90aa342
Set id: 6aaec5a4-701e-4870-896d-f68f62448c7a
Version: 5
Effective Time: 20231021
 
Amway Corp