Label: GLOW BODY MIST SPF 50- avobenzone, homosalate, octisalate, octocrylene spray

  • NDC Code(s): 30807-5005-1
  • Packager: WILD CHILD LABORATORIES PTY LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 24, 2023

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  • ACTIVE INGREDIENT

    AVOBENZONE 3% SUNSCREEN

    HOMOSALATE 10% SUNSCREEN

    OCTISALATE 5 % SUNSCREEN

    OCTOCRYLENR 8 % SUNSCREEN

  • USE

    Helps prevent Sunburn

    If used as directed with other sun Protection measure ( see directions), decrease the risk of skin cancer and early skin ageing caused by the sun

  • warning

    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 Product is swallowed , get medical help or contact a poison control center right away

  • Directions

    Generously spray to exposed areas holding bottle 10-15 cm away from skin. Ensure even application by spraying at least 7 times per section of body until product is visible, Rub in lightly.

    Use a water- resistant sunscreen if swimming or sweating.

    reapply at least every 2 hours.

    Children under 6 months of age : ask a doctor

  • Inactive Ingredients

    alcohol, Citrullius Lanatus Seed oil, Kakadu Plum, Tocopheryl Acetate, Fragrance

  • other information

    Protect the product in this container from excessive heat & direct sun

  • Sun Protection Measures

    Spending time in the Sun Increases your risk of skin cancer and early skin ageing. 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 10.00 AM - 2.00 PM

    Wea long-sleeved Shirts , pants hats, and sunglasses,

  • Purpose

  • Purpose

    Sunscreen

  • Label

    1

  • INGREDIENTS AND APPEARANCE
    GLOW BODY MIST  SPF 50
    avobenzone, homosalate, octisalate, octocrylene spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30807-5005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10.5 g  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE4.5 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE15 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE7.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    KAKADU PLUM (UNII: 0ZQ1D2FDLI)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATERMELON SEED OIL (UNII: L33J06UQTT)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30807-5005-1150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02009/01/2021
    Labeler - WILD CHILD LABORATORIES PTY LTD (890661643)
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