Label: MARY KAY TIMEWISE AGE MINIMIZE 3D DAY CREAM SPF 30 BROAD SPECTRUM SUNSCREEN (NORMAL TO DRY SKIN)- avobenzone, homosalate, octisalate, octocrylene, oxybenzone cream

  • NDC Code(s): 51531-9004-3, 51531-9004-7
  • Packager: Mary Kay Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 24, 2023

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

  • Active Ingredients

    Avobenzone 3%

    Homosalate 9%

    Octisalate 4.5%

    Octocrylene 3%

    Oxybenzone 4.5%

  • 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
  • Inactive ingredients

    water/eau, glycerin, dicaprylyl carbonate, cetearyl alcohol, dimethicone, ammonium acryloyldimethyltaurate/VP copolymer, ceteareth-25, niacinamide, saccharomyces cerevisiae extract, opuntia ficus-indica fruit extract, tocopheryl acetate, bisabolol, oligopeptide-1, resveratrol,  behenyl alcohol, jojoba esters, sucrose palmitate, disodium ethylene dicocamide PEG-15 disulfate, silica, hydroxypropyl cyclodextrin, 
    glyceryl linoleate, ethoxydiglycol, methyldihydrojasmonate, ethylene brassylate, tetramethyl acetyloctahydronaphthalenes, 
    ethyl linalool, isobutyl methyl tetrahydropyranol, methylenedioxyphenyl methylpropanal, phenylisohexanol, trimethylbenzenepropanol, 
    methyl benzodioxepinone, triethanolamine, disodium EDTA, sodium benzoate, ethylhexylglycerin, caprylhydroxamic acid, caprylyl glycol, propanediol, phenoxyethanol, iodopropynyl butylcarbamate.

  • 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 - 48 g carton

    Mary Kay

    timewise age minimize 3D day cream

    spf 30 broad spectrum sunscreen

    1.7 OZ. NET WT. / 48 g

    image of carton

  • INGREDIENTS AND APPEARANCE
    MARY KAY TIMEWISE AGE MINIMIZE 3D DAY CREAM SPF 30 BROAD SPECTRUM SUNSCREEN (NORMAL TO DRY SKIN) 
    avobenzone, homosalate, octisalate, octocrylene, oxybenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51531-9004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE9 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE3 g  in 100 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE4.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    CETEARETH-25 (UNII: 8FA93U5T67)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
    PRICKLY PEAR FRUIT (UNII: 18V8PAQ629)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    RESVERATROL (UNII: Q369O8926L)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)  
    SUCROSE PALMITATE (UNII: 3OSQ643ZK5)  
    DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    HYDROXYPROPYL .ALPHA.-CYCLODEXTRIN (UNII: ZFR0T80O4Y)  
    GLYCERYL MONOLINOLEATE (UNII: 4763AXI84L)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
    TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES (UNII: 2JU6ZH6GRE)  
    ETHYL LINALOOL (UNII: SF2JS9GF5T)  
    2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F)  
    3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA)  
    PHENYLISOHEXANOL (UNII: M56178H183)  
    TRIMETHYLBENZENEPROPANOL (UNII: 7S411YY2VY)  
    METHYL BENZODIOXEPINONE (UNII: 0NQ136C313)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51531-9004-71 in 1 CARTON05/16/2018
    148 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:51531-9004-39 g in 1 TUBE; Type 0: Not a Combination Product05/16/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02005/16/2018
    Labeler - Mary Kay Inc. (049994452)
    Establishment
    NameAddressID/FEIBusiness Operations
    Englewood Lab Inc.172198223manufacture(51531-9004)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mary Kay Inc.103978839manufacture(51531-9004)