Home > Drugs A-Z > Mary Kay TimeWise Day Solution SPF 35

Mary Kay TimeWise Day Solution SPF 35 (Mary Kay Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION 14 mL in 1 BOTTLE, PUMP (51531-8360-5) Label Information
SOLUTION 1 BOTTLE, PUMP in 1 CARTON (51531-8360-1) > 29 mL in 1 BOTTLE, PUMP Label Information

Complete Mary Kay TimeWise Day Solution SPF 35 Information

  • Active Ingredients

    Avobenzone 2%

    Homosalate 10%

    Octisalate 5%

    Octocrylene 2%

    Oxybenzone 4%


  • 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 warm 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

  • Inactive ingredients

    water, dimethicone, butylene glycol, styrene/acrylates copolymer, C12-15 alkyl

    benzoate, dicaprylyl carbonate, glycerin, ceteareth-25, dimethicone crosspolymer,

    magnesium aluminum silicate, acetyl dipeptide-1 cetyl ester, plankton extract,

    hydrolyzed algin, pentylene glycol, tocopheryl acetate, crithmum maritimum extract,

    ascorbic acid, hydrogenated lecithin, hydroxyethylcellulose, dipropylene glycol

    dibenzoate, acrylates/C12-22 alkyl methacrylate copolymer, disodium ethylene

    dicocamide PEG-15 disulfate, sorbic acid, caprylyl glycol, PPG-15 stearyl ether benzoate,

    propylene glycol, xanthan gum, cyclopentasiloxane, PEG-75, PEG-150, PEG-8 cetyl

    dimethicone, PEG-4 laurate, laureth-3, disodium EDTA, ammonium hydroxide,

    iodopropynyl butylcarbamate, phenoxyethanol


  • Other information

    • protect this product from excessive heat and direct sun
    • store above 32°F / 0°C

  • Questions or comments?

    Call toll free 1-800-627-9529


  • Principal Display Panel - 29 mL carton

    Mary Kay

    timewise day solution

    sunscreen

    broad spectrum

    spf 35

    1 FL. OZ. / 29 mL

    Image of carton


  • INGREDIENTS AND APPEARANCE
    MARY KAY TIMEWISE DAY SOLUTION SPF 35 
    avobenzone, homosalate, octisalate, octocrylene, oxybenzone solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51531-8360
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2 g  in 100 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 4 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETEARETH-25 (UNII: 8FA93U5T67)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    DIPROPYLENE GLYCOL DIBENZOATE (UNII: 6OA5ZDY41O)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PPG-15 STEARYL ETHER BENZOATE (UNII: 80D2J6361M)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PEG-4 LAURATE (UNII: AYF4VM3N1Z)  
    SORBIC ACID (UNII: X045WJ989B)  
    LAURETH-3 (UNII: F32E4CB0UJ)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    ACETYL DIPEPTIDE-1 CETYL ESTER (UNII: 3M7W78X5IR)  
    AMMONIA (UNII: 5138Q19F1X)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CRITHMUM MARITIMUM (UNII: J7IHY79BKY)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  
    POLYETHYLENE GLYCOL 7000 (UNII: Q0JET65GEL)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51531-8360-1 1 in 1 CARTON
    1 29 mL in 1 BOTTLE, PUMP
    2 NDC:51531-8360-5 14 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part352 03/01/2012
    Labeler - Mary Kay Inc. (103978839)
    Establishment
    Name Address ID/FEI Business Operations
    Mary Kay Inc. 103978839 manufacture(51531-8360)