Label: BONDI SANDS SUNNY DAZE HYDRATING BROAD SPECTRUM SUNSCREEN SPF 50- zinc oxide lotion

  • NDC Code(s): 70157-020-01
  • Packager: Baxter Laboratories Pty. Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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  • Active Ingredients

    Zinc Oxide 25%

  • 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.

    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 this product

    keep out of eyes. Rinse with water to remove.

  • Directions

    • Apply liberally 15 minutes before sun exposure.
    • Reapply:
    • Every 2 hours
    • Use a water resistant sunscreen if swimming or sweating.
    • 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 888-266-0772; Monday – Friday, 9 am – 5 pm.
  • Inactive Ingredients

    Water, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Glycerin, Polyhydroxystearic Acid, Cetearyl Alcohol, Phenoxyethanol, Polyurethane-62, Benzyl Alcohol, Saccharide Isomerate, Citric Acid, Propanediol, Lecithin, Xanthan Gum, Sodium Phytate, Ethylhexylglycerin, Trideceth-6, Tocopherol, Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Sodium Citrate, Erythritol, Hibiscus Sabdariffa Fruit Extract, Iron Oxides.

  • Questions?

    888-266-0772 or visit bondisands.com

  • Product Packaging

    bondi sands

    Everyday skincare

    Sunny

    Daze

    HYDRATING

    BROAD SPECTRUM

    SUNSCREEN SPF 50

    + HIBISCUS FRUIT EXTRACT

    Australian Made

    1.76 OZ. (50g)

    sunny daze

  • INGREDIENTS AND APPEARANCE
    BONDI SANDS SUNNY DAZE HYDRATING BROAD SPECTRUM SUNSCREEN SPF 50 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70157-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE250 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ERYTHRITOL (UNII: RA96B954X6)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    HIBISCUS SABDARIFFA WHOLE (UNII: UH3Z91Y49Y)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PHYTATE SODIUM (UNII: 88496G1ERL)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    POLYURETHANE-62 (UNII: TBK645J3J8)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70157-020-011 in 1 CARTON08/25/2021
    150 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/25/2021
    Labeler - Baxter Laboratories Pty. Ltd. (740537709)
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