Label: BOSCIA DAILY DEFENSE SUNSCREEN BROAD SPECTRUM SPF 50 PA- octinoxate, titanium dioxide, zinc oxide cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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  • Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA


  • Active Ingredients

    Octinoxate  7.25% Titanium Dioxide 5.74% Zinc Oxide  4.75%


  • 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.  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

    • Apply liberally 15 minutes before sun exposure
    • Use a water resistant sunscreen if swimming or sweating
    • Reapply at least every 2 hours
    • Optional: apply to all skin exposed to the sun
    • 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 broadspectrum SPF of 15 or higher and another sun protection measures including: Sun Protection Measures.
    • Limit time in the usn, especially from 10 a.m. - 2 p.m.
    • wear long-sleeve shirts, pants, hats, and sunglasses.
    • Children under 6 months:  Ask a doctor
  • Inactive Ingredients:

    Cyclopentasiloxane, Water/Aqua/Eau, PEG-10 Dimethicone, Butylene Glycol, Glycerin, Caprylyl Methicone, Isodecyl Neopentanoate, Methylcellulose, Aluminum Starch Octenylsuccinate, Disteardimonium Hectorite, Sodium Chloride, Alumina, Dipropylene Glycol, Dimethicone/Vinyl Dimethicone Crosspolymer, Camellia Oleifera Leaf Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Dipotassium Glycyrrhizate, Sodium Hyaluronate, Tocopheryl Acetate, Panthenol, Sodium Levulinate, Sodium PCA, Methicone, Sodium Anisate, Silica, Caprylyl Glycol.

  • Other information

    • protect this product from excessive heat and sun
  • Questions or comments?

    Call toll free 1-888-635-8884

  • SPL UNCLASSIFIED SECTION

    This dual-action, anti-aging formula absorbs quickly for maximum protection. and absorb UVA and UVB rays to prevent skin damage. (water storing) ingredients and help certain moisture. and deliver antioxidant benefits to help prevent free radical damage while nourishing skin. Titanium Dioxide, Zinc OxideOctinoxateHygroscopicSodium PCA, Pre Vitamin B5Hylauronic AcidGreen Tea ExtractVitamin E Acetate

      Artificial fragrance and color free.  Gluten-free.  Ethanol alcohol-free.  Dermatologist tested.      www.boscia.net   B212-01   Distributed by   boscia, LLC.  Irvine, CA 92614    Made in USA Preservative-free.

  • PRINCIPAL DISPLAY PANEL

    boscia   Daily Defense Sunscreen Broad Spectrum SPF 50 PA+++     1.7 oz / 50 g For all skin types

  • Product Labels

    Inner LabelOuter Label

  • INGREDIENTS AND APPEARANCE
    BOSCIA DAILY DEFENSE SUNSCREEN BROAD SPECTRUM SPF 50 PA 
    octinoxate, titanium dioxide, zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76151-241
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.25 g  in 100 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE5.742 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE4.75 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)  
    EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)  
    JOJOBA OIL (UNII: 724GKU717M)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SODIUM LEVULINATE (UNII: VK44E1MQU8)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    SODIUM ANISATE (UNII: F9WFJ28MV9)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76151-241-0150 g in 1 TUBE; Type 0: Not a Combination Product12/19/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/07/2012
    Labeler - Boscia LLC (967960951)
    Establishment
    NameAddressID/FEIBusiness Operations
    Englewood Lab, Inc.172198223manufacture(76151-241)
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