Label: SALT AND STONE LIGHTWEIGHT SHEER MINERAL SUNSCREEN SPF30- zinc oxide lotion

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

Drug Label Information

Updated October 28, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active Ingredients

    Zinc Oxide (Non-Nano) 15.7%

    Purpose

    Sunscreen

  • Uses

    • Helps prevent sunburn
    • If used as directed with other skin 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 immediately.

  • Directions

    • Apply liberally 15 minutes before sun exposure
    • Reapply at least every 2 hours
    • Use a water resistant sunscreen if swimming or sweating
    • Sun protection Measures.
    • Limit time in the sun, especially from 10am - pm.
    • Wear long-sleeved shirts, pants, hats, and sunglasses.

    Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

    Children under 6 months: Ask a doctor

  • Other Information

    • Protect this product from excessive heat and direct sun.
  • Inactive Ingredients

    Aloe Barbadensis Leaf Juice, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Caprylhydroxamic Acid, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetyl Alcohol, Chondrus Crispus Extract, Diisostearoyl Polyglyceryl-3 Dimer Dilinoleate, Ethylhexyl Olivate, Glycerin, Glyceryl Behenate/Eicosadioate, Isododecane, Isopropyl Myristate, Jojoba Esters, Laminaria Digitata Extract, Macrocystis Pyrifera (Keip) Extract, Magnesium Sulfate, Niacinamide, Polyglyceryl-3 Oleate, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Polyglyceryl-4 Diisostearate, Polyhydroxystearic Acid, Propanediol, Sodium Gluconate, Squalane, Tocopherol, Trihydroxystearin, Water, Xanthan Gum.

  • Questions or Comments?

    info@saltandstone.com

  • Package Labeling:

    Outer PackageInner Package

  • INGREDIENTS AND APPEARANCE
    SALT AND STONE LIGHTWEIGHT SHEER MINERAL SUNSCREEN SPF30 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71585-144
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION157 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)  
    DIISOSTEAROYL POLYGLYCERYL-3 DIMER DILINOLEATE (UNII: G3232Z5S2O)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR)  
    ISODODECANE (UNII: A8289P68Y2)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    LAMINARIA DIGITATA (UNII: 15E7C67EE8)  
    MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    POLYGLYCERYL-3 OLEATE (UNII: XRQ165498B)  
    POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    SQUALANE (UNII: GW89575KF9)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    TRIHYDROXYSTEARIN (UNII: 06YD7896S3)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71585-144-001 in 1 BOX09/01/2023
    160 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02009/01/2023
    Labeler - SALT & STONE, INC. (080683697)