Label: MARY KAY CC CREAM SUNSCREEN BROAD SPECTRUM SPF 15 MEDIUM TO DEEP- homosalate, octinoxate, oxybenzone cream

  • NDC Code(s): 51531-2824-1, 51531-2824-3
  • Packager: Mary Kay Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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

  • Active ingredients

    Homosalate 5%

    Octinoxate 6.5%

    Oxybenzone 1.2 %

  • 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
    • 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 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-sleeve shirts, pants, hats and sunglasses
    • children under 6 months: Ask a doctor
  • Other information

    • Store at 25°C (77°F). Do not freeze or refrigerate.
  • Inactive ingredients

    water, cyclopentasiloxane, butylene glycol, glycerin, PEG-9 polydimethylsiloxyethyl dimethicone, niacinamide, mica, PEG-9 dimethicone, magnesium sulfate, ascorbyl glucoside, silybum marianum fruit extract, tocopheryl acetate, salix nigra (willow) bark extract, salicylic acid, adenosine, dimethicone/PEG-10/15 crosspolymer, disodium stearoyl glutamate, xanthan gum, dipropylene glycol, disodium EDTA, cyclohexasiloxane, sodium citrate, tocopherol, sorbic acid, sodium benzoate, benzyl alcohol, aluminum hydroxide, titanium dioxide, iron oxides

  • Questions or comments?

    Call toll free 1-800-627-9529

  • Principal Display Panel - 29 mL carton

    Mary Kay

    cc cream

    sunscreen broad

    spectrum spf 15

    cream

    1 FL. OZ. / 29 mL

    image of carton

  • INGREDIENTS AND APPEARANCE
    MARY KAY CC CREAM SUNSCREEN BROAD SPECTRUM SPF 15 MEDIUM TO DEEP 
    homosalate, octinoxate, oxybenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51531-2824
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE5 g  in 100 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE6.5 g  in 100 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE1.2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    MICA (UNII: V8A1AW0880)  
    PEG-9 DIMETHICONE (400 CST) (UNII: 9OZ27X065D)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)  
    MILK THISTLE (UNII: U946SH95EE)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SALIX NIGRA BARK (UNII: QU52J3A5B3)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    ADENOSINE (UNII: K72T3FS567)  
    DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    SORBIC ACID (UNII: X045WJ989B)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51531-2824-11 in 1 CARTON02/16/2014
    129 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:51531-2824-31 mL in 1 PACKET; Type 0: Not a Combination Product02/16/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/16/2014
    Labeler - Mary Kay Inc. (049994452)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mary Kay Inc.103978839manufacture(51531-2824)
    Establishment
    NameAddressID/FEIBusiness Operations
    Englewood Lab Inc.172198223manufacture(51531-2824)