Label: SALT AND STONE SPF 30 SUNSCREEN STICK- zinc oxide stick

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

Drug Label Information

Updated October 28, 2023

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  • DRUG FACTS

  • Active Ingredients

    Zinc Oxide (Non-Nano) 22.5%

    Purpose

    Sunscreen

  • Uses

    • Hepls 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.

    If rash occurs

    stop use and see a doctor.

    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.
    • Reapply:
    • After 80 minutes of swimming or sweating,
    • Immediately after towel drying.
    • At least every two (2) hours.
    • Spending time in the sun increases the risk of skin cancer and early skin aging. To decrease the risk, regularly use: a suscreen with a broad-spectrum measures including: Sun Protection Measures
    • Limiting time in the sun, especially from 10AM - 2PM.
    • Wear long-sleeved shirts, pants, hats, and sunglasses.
    • Children under 6 months: Ask a doctor.
  • Other Information

    Protect this product from excess heat and direct sun.

  • Inactive Ingredients

    (Shea) Butter, Cera Alba (Beeswax)*, (Carnauba) Wax,* (Coconut) Oil,* (Sunflower) Seed Oil,* Butyrospermum ParkiiCopernicia CeriferaCocos NuciferaHelianthus AnnuusMica, Silica, Simmondsia Chinensis (Jojoba) Seed Oil,* Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate.

    *Organic Ingredient

  • Package Labeling:

    Outer Package2Inner Package2

  • INGREDIENTS AND APPEARANCE
    SALT AND STONE SPF 30 SUNSCREEN STICK 
    zinc oxide stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71585-141
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION225 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SHEA BUTTER (UNII: K49155WL9Y)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    MICA (UNII: V8A1AW0880)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    JOJOBA OIL (UNII: 724GKU717M)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71585-141-0015 g in 1 TUBE; Type 0: Not a Combination Product09/22/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02009/22/2021
    Labeler - Salt and Stone (080683697)
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