Label: ARTISTRY BEAUTY BALM PERFECTING PRIMER SPF 35 BROAD SPECTRUM SUNSCREEN- ensulizole, octinoxate, zinc oxide cream
- NDC Code(s): 50390-004-30
- Packager: Amway Corp
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 21, 2023
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Other Information
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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).
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Directions
For suncreen use
- Apply liberally 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating or washing
- Reapply at least every 2 hours
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: ■ limit time in the sun, especially from 10 a.m. – 2 p.m. ■ wear long-sleeve shirts, pants, hats, and sunglasses Sun Protection Measures.
- Children under 6 months: ask a doctor
- Package Labeling
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INGREDIENTS AND APPEARANCE
ARTISTRY BEAUTY BALM PERFECTING PRIMER SPF 35 BROAD SPECTRUM SUNSCREEN
ensulizole, octinoxate, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50390-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE 20 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 54.9 mg in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:50390-004-30 30 mL in 1 TUBE; Type 0: Not a Combination Product 05/05/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/05/2015 Labeler - Amway Corp (083416854) Establishment Name Address ID/FEI Business Operations Access Business Group LLC 839830713 manufacture(50390-004)
