Label: SHEGLAM DEW AND DONE SKIN TINT WITH SPF 20 NUTMEG- zinc oxide cream

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

Drug Label Information

Updated January 2, 2025

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  • Drug Facts

  • Active ingredient

    Zinc Oxide 14.625%

    Purpose

    Sunscreen

  • Use

    • helps prevent sunburn
  • Warnings

    Skin Cancer/Skin Aging Alert:Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. 

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

  • Directions

    • apply liberally 15 minutes before sun exposure
    • reapply at least every 2 hours
    • use a water resistant sunscreen if swimming or sweating 
    • children under 6 months of age: Ask a doctor
  • Other information

    • protect the product in this container from excessive heat and direct sun
  • Inactive ingredients

    Water, Glycerin, Dimethicone, Caprylyl Methicone, C9-12 Alkane, Butylene Glycol, Butyloctyl Salicylate, Dimethicone/PEG-10/15 Crosspolymer, Trimethylsiloxysilicate, Jojoba Seed Oil, Oryzanol, Isononyl Isononanoate, Magnesium Sulfate, 1,2-Hexanediol, PEG-10 Dimethicone, Hydroxyacetophenone, Triethoxycaprylylsilane, Sodium Hyaluronate, Dipropylene Glycol, Sodium Citrate, Gotu Kola Leaf Extract, Bisabolol, Tocopherol, Snow Lotus Extract, Xylitylglucoside, Anhydroxylitol, Xylitol, Ethylhexylglycerin, Ginger Root Extract, Titanium Dioxide Color, Iron Oxides Color.

  • Package Labeling:

    Outer Label Nutmeg.jpgInner Label Nutmeg.jpg

  • INGREDIENTS AND APPEARANCE
    SHEGLAM DEW AND DONE SKIN TINT WITH SPF 20 NUTMEG 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85068-023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION146.25 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    BISABOLOL (UNII: 24WE03BX2T)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)  
    ANHYDROXYLITOL (UNII: 8XWR7NN42F)  
    XYLITOL (UNII: VCQ006KQ1E)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GINGER (UNII: C5529G5JPQ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CAPRYLYL METHICONE (UNII: Q95M2P1KJL)  
    C9-12 ALKANE (UNII: 7J5R5W72QM)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)  
    JOJOBA OIL (UNII: 724GKU717M)  
    ORYZANOL (UNII: SST9XCL51M)  
    ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85068-023-011 in 1 CARTON05/30/2025
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/30/2025
    Labeler - EVER FAME PTE. LTD. (659974769)
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