Label: MINERAL SUNSCREEN SPF 30- zinc oxide spray

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 11, 2022

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  • ACTIVE INGREDIENT

    ​Active Ingredients                                    Purpose

    Zinc Oxide 12.0% ..................................... Sunscreen

  • PURPOSE

    ​Uses

    • 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
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    Stop use and ask a doctor is rash occurs

  • WARNINGS

    Warnings

    • For external use only
    • Flammable: Contents under pressure. Do not punture or incinerate. Do not store at temperatures above 120 F. Do not use in the precesne of a flame or spark, or while smoking
    • Do not use on damaged or broken skin
    • When using this product keep out of eyes
    • Rinse with water to remove
    • Keep out of reach of children
    • If swallowed, get medical help or contact a Poison Control Center right away

  • DOSAGE & ADMINISTRATION

    ​Directions

    ​SHAKE WELL to activate. If the mist is clear, keep shaking.

    • Apply liberally 15 minutes before sun exposure
    • Reapply:

    - after 80 minutes of swimming or sweating

    - immediately after towel drying

    - at least every 2 hours whem exposed to sunlight

    • Children un 6 months: Ask a doctor

    ​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 epsecially from 10 a.m. - 2 p.m.
    • Wear long-sleeved shirts, pants, hats, and sunglasses
  • INACTIVE INGREDIENT

    Aloe Barbadensis Leaf Juice, Bentonite, Butyloctyl Salicylate, Calendula Officinalis Flower Extract, Caprylhydroxamic Acid, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Seed Oil, Cetearyl Alcohol, Chamomilla Recutita (Matricaria) Flower Extract, Coco Glucoside, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Heptyl Undecylenate, Jojoba Esters, Melissa Officinalis Leaf Extract, Methyl Dihydroabietate, Nasturtium Officinale Flower/Leaf Extract, Spiraea Ulmaria Flower Extract, Water

  • PRINCIPAL DISPLAY PANEL

    Supergoop!

    Play

    SPF 30

    100% Mineral Body Mist

    with Marigold Extract

    Broad Spectrum Sunscreen SPF 30

    Water Resistant (80 minutes)

    6 fl. oz. / 177 mL.

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    MINERAL SUNSCREEN SPF 30 
    zinc oxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75936-510
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION12 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)  
    HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)  
    METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)  
    NASTURTIUM OFFICINALE FLOWERING TOP (UNII: W1N2U8I64G)  
    FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENTONITE (UNII: A3N5ZCN45C)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CHAMOMILE (UNII: FGL3685T2X)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75936-510-01177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/15/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35205/15/2017
    Labeler - Supergoop, LLC (117061743)