Label: DOTERRA SUN FACE DAILY MOISTURIZER- zinc oxide lotion

  • NDC Code(s): 71630-147-15
  • Packager: doTERRA International, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient Purpose
    Zinc Oxide 13%.......................................... Sunscreen

  • Mineral Sunscreen Daily Moisturizer

    This dermatologist-tested, mineral-based, broad-spectrum
    sun protection moisturizer delivers exponential
    benefits so your skin can look and act as young as
    you feel. Formulated with non-nano zinc oxide,
    doTERRA sun Face Mineral Sunscreen Daily Moisturizer
    provides lightweight SPF 28 UVA/UVB defense
    against the sun and blue light protection.
    Rich in antioxidants, vitamin E, and nourishing
    botanicals such as evodia, grapeseed oil, and CPTG®
    essential oils, this lightweight, hydrating sunscreen
    moisturizer is intended for everyday use.

  • INDICATIONS & USAGE

    Helps prevent sunburn •If used as directed
    with other sun protection measures (see Directions),
    decreases the risk of skin cancer and early skin aging
    caused by the sun

  • WARNINGS

    For external use only
    Do not use on damaged or broken 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 swallowed, get medical
    help or contact a Poison Control Center right away.

  • WHEN USING

    For sunscreen use: • apply liberally 15 minutes before
    sun exposure • apply to all skin exposed to the sun •
    use a water resistant sunscreen if swimming or sweating
    • reapply at least every 2 hours
    †Children under 6 months: Ask a doctor

  • OTHER SAFETY INFORMATION

    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 value 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-sleeved shirts, pants, hats, and sunglasses

  • INACTIVE INGREDIENT

    Inactive ingredients Water (Aqua), Caprylic/Capric
    Triglyceride, Butyloctyl Salicylate, Propanediol, Vitis
    vinifera (Grape) Seed Oil, Cetearyl Alcohol, Cetyl
    Alcohol, Evodia rutaecarpa (Evodia) Fruit Extract,
    Persea gratissima (Avocado) Oil, Daucus carota sativa
    (Carrot) Seed Oil, Boswellia carterii (Frankincense) Oil,
    Helichrysum italicum Flower/Leaf/Stem Oil,
    Astrocaryum tucuma Seed Butter, Rubus idaeus
    (Raspberry) Seed Oil, Sodium Stearoyl Glutamate,
    Arachidyl Alcohol, Caprylyl Glycol, Coco-Glucoside,
    Xanthan Gum, Helianthus annuus (Sunflower) Seed Oil,
    Cocos nucifera (Coconut) Fruit Extract, Michelia alba
    (Magnolia) Leaf Oil, Cymbopogon flexuosus
    (Lemongrass) Oil, Cananga odorata (Ylang Ylang)
    Flower Oil, Aloe barbadensis Leaf Juice, Michelia alba
    (Magnolia) Flower Oil, Ethyl Ferulate, Behenyl Alcohol,
    Arachidyl Glucoside, Citric Acid, Sodium Gluconate,
    Bisabolol, Caprylhydroxamic Acid, Tocopherol,
    Polyhydroxystearic Acid, Phytosterols, Squalene, Citrus
    nobilis (Mandarin Orange) Peel Oil

  • STORAGE AND HANDLING

    Other information • protect this product from
    excessive heat and direct sun.

  • QUESTIONS

    Questions or comments? Call 1-800-411-8151

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • DOSAGE & ADMINISTRATION

    Apply topically

  • doTERRA sun Face Mineral Sunscreen Daily Moisturizer

    Sun Face Moisturizer 50ml US PumpSun Face Moisturizer 50ml Pump US CartonPrimary Label and Packaging

  • INGREDIENTS AND APPEARANCE
    DOTERRA SUN FACE DAILY MOISTURIZER 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71630-147
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ASTROCARYUM MURUMURU SEED BUTTER (UNII: 12V64UPU6R)  
    CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)  
    CITRUS NOBILIS WHOLE (UNII: U29I7N5FLM)  
    CYMBOPOGON FLEXUOSUS WHOLE (UNII: 0MK18YOA5G)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    EVODIA RUTAECARPA FRUIT, IMMATURE (UNII: F7M0RB6Y4I)  
    MICHELIA ALBA LEAF OIL (UNII: 002RK9L1FN)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)  
    ETHYL FERULATE (UNII: 5B8915UELW)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    GLUCOSE PENTAACETATE (UNII: 3040885R4N)  
    RASPBERRY SEED OIL (UNII: 9S8867952A)  
    DODECANEDIOIC ACID (UNII: 978YU42Q6I)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)  
    CARROT SEED OIL (UNII: 595AO13F11)  
    COCOS NUCIFERA WHOLE (UNII: 245J88W96L)  
    MICHELIA ALBA WHOLE (UNII: TKZ4AVY41O)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    GRAPE SEED OIL (UNII: 930MLC8XGG)  
    .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    BUTYLOCTANOL (UNII: N442D9VO79)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    SQUALENE (UNII: 7QWM220FJH)  
    WATER (UNII: 059QF0KO0R)  
    AVOCADO OIL (UNII: 6VNO72PFC1)  
    HELICHRYSUM ITALICUM FLOWER OIL (UNII: O97ZV7726K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71630-147-1550 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/01/2023
    Labeler - doTERRA International, LLC (832274935)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bell International Laboratories967781555manufacture(71630-147)
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