Label: BONDI SANDS SPF 60 SUNNY SPRITZ FACE MIST- homosalate, octocrylene, octisalate, avobenzone aerosol, spray

  • NDC Code(s): 79950-016-01
  • Packager: BONDI SANDS (USA) INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 6, 2025

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  • Drug Facts

  • Active Ingredients

    Avobenzone 3%

    Homosalate 10.5%

    Octisalate 3.5%

    Octocrylene 5.6%

  • Purpose

    Sunscreen

  • 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.
  • Warnings

    • For external use only.

    Do not use

    on damaged or broken skin.

    When using this product

    keep out of eyes. If eye contact occurs, rinse thoroughly with clean running water.

    Stop use and ask a doctor

    if rash or irritation occurs.

    Keep out of reach of children.

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

    Flammable. Warning.

    Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F. Keep out of reach of children. Use only as directed. Intentional misuse by deliberately concentrating and inhaling can be harmful or fatal.

  • Directions

    • Shake well before use.
    • Hold spray 8-10 inches away from face with eyes and mouth closed before using.
    • Do not apply the product in windy conditions.
    • Apply liberally and evenly 15 minutes before sun exposure.
    • Use a water resistant sunscreen if swimming or sweating.
    • Reapply:
    • 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 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.
    • Children under 6 months: Ask a doctor.
  • Other Information

    • Protect the product in this container from excessive heat and direct sun.
    • You may report a serious adverse reaction to 888-339-7642; Monday-Friday, 9 am - 5 pm.
  • Inactive Ingredients

    Alcohol Denat., Butane, Isobutane, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Acrylates/Octylacrylamide Copolymer, Cyclopentasiloxane, Diethylhexyl 2,6-Naphthalate, Glycerin, Water/Aqua/Eau, Propane, Erythritol, Tocopheryl Acetate, Hibiscus Sabdariffa Fruit Extract

  • Questions?

    888-339-7642 or visit bondisands.com

  • Product Labeling

    1

  • INGREDIENTS AND APPEARANCE
    BONDI SANDS SPF 60 SUNNY SPRITZ FACE MIST 
    homosalate, octocrylene, octisalate, avobenzone aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79950-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE35 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE56 mg  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE105 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    BUTANE (UNII: 6LV4FOR43R)  
    CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)  
    ERYTHRITOL (UNII: RA96B954X6)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPANE (UNII: T75W9911L6)  
    ISOBUTANE (UNII: BXR49TP611)  
    ACRYLATES/OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79950-016-011 in 1 CARTON01/06/2025
    160 g in 1 CAN; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/06/2025
    Labeler - BONDI SANDS (USA) INC. (117596864)
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