Label: ARTISTRY HYDRO-V SHEER WEIGHTLESS FOUNDATION SPF 15 BROAD SPECTRUM SUNSCREEN- octinoxate, zinc oxide cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 21, 2023

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  • Drug Facts

  • Active Ingredients

    Octinoxate 4% (W/W P/P)

    Zinc Oxide 2.74% (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.

  • Directions

    For suncreen use

    • Apply liberally 15 minutes before sun expos
    • Use a water resistant sunscreen if swimming or sweating or washing
    • Reapply at least every 2 hours
    • Sun Protection Measures. 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
    • Children under 6 months: ask a doctor
  • Other Information

    • Protect this product from excessive heat and direct sun
  • Inactive ingredients

    WATER/AQUA/EAU, DIMETHICONE, DIPHENYLSILOXY PHENYL TRIMETHICONE, NEOPENTYL GLYCOL DIHEPTANOATE, MICA (CI 77019), LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, SILICA, TRIMETHYLSILOXYPENYL DIMETHICONE, CYCLOPENTASILOXANE, PENTYLENE GLYCOL, PROPANEDIOL, GLYCERIN, C12-15 ALKYL BENZOATE, DIPHENYL DIMETHICONE, SYNTHETIC FLUORPHLOGOPITE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, ETHYLHEXYL PALMITATE, LECITHIN, HYDROXYACETOPHENONE, DISTEARDIMONIUM HECTORITE, POLYSILICONE-11, ALUMINA, POLYSORBATE-20, SODIUM CHLORIDE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, ALCOHOL DENAT, PEG/PPG-18/18 DIMETHICONE, ISOCETETH-10, TRISILOXANE, TRIETHOXYCAPRYLYLSILANE, HYDROGEN DIMETHICONE, PHENOXYETHANOL, DISODIUM EDTA, SODIUM HYALURONATE, BUTYLENE GLYCOL, EUTERPE OLERACEA FRUIT OIL, LAURETH-12, DIPROPYLENE GLYCOL, BHT, TOCOPHEROL, CHLORPHENESIN, GLYCINE SOJA (SOYBEAN) OIL, CERAMIDE NP, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, BETA-SITOSTEROL, PROPYLENE GLYCOL, PERILLA OCYMOIDES SEED OIL, SALVIA HISPANICA SEED OIL, OENOTHERA BIENNIS (EVENING PRIMROSE) OIL, TETRAHEXYLDECYL ASCORBATE. MAY CONTAIN / PEUT CONTIENIR +/- IRON OXIDES (CI 77491, 77492, 77499), TITANIUM DIOXIDE (CI 77891).

  • Package Labeling:

    Shade StickerLabel5

  • INGREDIENTS AND APPEARANCE
    ARTISTRY HYDRO-V SHEER WEIGHTLESS FOUNDATION SPF 15 BROAD SPECTRUM SUNSCREEN 
    octinoxate, zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50390-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE40 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION27.4 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    MICA (UNII: V8A1AW0880)  
    LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALCOHOL (UNII: 3K9958V90M)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    ISOCETETH-10 (UNII: 1K92T9919H)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ACAI OIL (UNII: Z0W6766A2W)  
    LAURETH-12 (UNII: OAH19558U1)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    CERAMIDE NP (UNII: 4370DF050B)  
    MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)  
    .BETA.-SITOSTEROL (UNII: S347WMO6M4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PERILLA FRUTESCENS SEED OIL (UNII: 322MS57V7Z)  
    CHIA SEED OIL (UNII: MC2LH51BO7)  
    EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50390-014-001 in 1 CARTON09/23/2017
    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 DrugM02009/23/2017
    Labeler - Amway Corp (083416854)
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