Label: PLAY EVERYDAY SUNSCREEN SPF 50 WITH SUNFLOWER EXTRACT- avobenzone, homosalate, octisalate, octocrylene cream

  • NDC Code(s): 75936-236-01, 75936-236-02, 75936-236-03, 75936-236-04, view more
    75936-236-05, 75936-236-06
  • Packager: Supergoop, LLC
  • 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 July 11, 2023

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  • ACTIVE INGREDIENT

    Active Ingredients Purpose

    Avobenzone 3% Sunscreen

    Homosalate 10% Sunscreen

    Octisalate 5% Sunscreen

    Octocrylene 7.5% 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 if rash occurs

  • 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

    If swallowed, get medical help or contact a Poison Control Center right away

  • DOSAGE & ADMINISTRATION

    Directions

    • Apply liberally 15 minutes before sun exposure

    Reapply:

    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • 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 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-sleeved shirts, pants, hats, and sunglasses
    • Children under 6 months: Ask a doctor
  • INACTIVE INGREDIENT

    Water, Acrylates Copolymer,  Diisopropyl Sebacate, Glycerin, Isodecyl Neopentanoate, Isododecane, Lauryl Lactate, Cetyl Alcohol, Potassium Cetyl Phosphate, Brassica Camprestris/Aleurites Fordi Copolymer, Oryza Sativa (Rice) Bran Extract, Cetearyl Olivate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Hydroxyacetophenone, Sorbitan Olivate, Diethylhexyl Syringylidenemalonate, Aniba Rosaeodora (Rosewood) Wood Oil, Chlorphenesin, Citrus Aurantium Dulcis (Orange) Peel Oil, ​ Citrus Limon (Lemon) Peel Oil, Ethylhexylglycerin, Eucalyptus Globulus Leaf Oil, Ocimum Bascilicum (Basil) Flower/Leaf Extract, Pelargonium Graveolens Flower Oil, Pogostemon Cablin Oil, Pentylene Glycol, 1,2-hexanediol, Caprylyl Glycol, Xanthan Gum, Helianthus Annuus (Sunflower) Extract, Behenic Acid, Cetyl Behenate, Isostearyl Isostearate, Trisodium Ethylenediamene Disuccinate, Tocopherol, Allantoin, Rosmarinus Officinalis (Rosemary) Leaf Extract, Caprylic/Capric Triglyceride,Panthenol, Pentasodium Triphosphate, Citric Acid

  • PRINCIPAL DISPLAY PANEL

    Supergoop!

    PLAY

    SPF 50

    Everyday Lotion with Sunflower Extract

    Broad Spectrum SPF 50 PA++++

    Water & Sweat Resistant (80 minutes)

    2.4 fl. oz./ 71 ml.

    CartonTube

  • INGREDIENTS AND APPEARANCE
    PLAY EVERYDAY SUNSCREEN SPF 50 WITH SUNFLOWER EXTRACT 
    avobenzone, homosalate, octisalate, octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75936-236
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE10 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE7.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    WATER (UNII: 059QF0KO0R)  
    DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)  
    ISODODECANE (UNII: A8289P68Y2)  
    LAURYL LACTATE (UNII: G5SU0BFK7O)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    RICE BRAN (UNII: R60QEP13IC)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
    ROSEWOOD OIL (UNII: F2522O5L7B)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LEMON OIL (UNII: I9GRO824LL)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2)  
    PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)  
    POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    BEHENIC ACID (UNII: H390488X0A)  
    CETYL BEHENATE (UNII: WFM51TRO3E)  
    ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ROSEMARY (UNII: IJ67X351P9)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75936-236-013 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2020
    2NDC:75936-236-0210 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2020
    3NDC:75936-236-0330 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2020
    4NDC:75936-236-0471 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2020
    5NDC:75936-236-05162 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2020
    6NDC:75936-236-06532 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35201/01/2020
    Labeler - Supergoop, LLC (117061743)
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