Label: BOTANICAL EFFECTS MOISTURIZER SPF 30- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated August 24, 2020

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  • PURPOSE

    UVA/UVB Protection

  • Warnings:

    For external use only, not to be swallowed.

    Avoid contact with eyes.

    Discontiunue use if signs of rash or irritation appear.

    Keep out of reach of children.

    Do not stay too long in the sun, even while using a sunscreen product.

    Overexposure to the sun is dangerous.

    Contains Benzophenone-3.

  • Directions:

    Apply liberally prior to sun exposure.

    Reapply frequently to maintain protection.

  • Ingredients:

    AQUA, HOMOSALATE, ALCOHOL DENAT., CYCLOPENTASILOXANE, BIOSACCHARIDE GUM-1, BENZOPHENONE-3, ETHYLHEXYL SALICYLATE, BUTYLENE GLYCOL, BUTYL METHOXYDIBENZOYLMETHANE, OCTOCRYLENE, ALOE BARBADENSIS LEAF EXTRACT, HYLOCEREUS UNDATUS FRUIT EXTRACT, DIPOTASSIUM GLYCYRRHIZATE, GLYCERIN, CYCLOHEXASILOXANE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, SODIUM ACRYLATES CROSSPOLYMER-2, METHYLDIHYDROJASMONATE, ISOBUTYL METHYL TETRAHYDROPYRANOL, SILICA, DISODIUM EDTA, ETHYLENE BRASSYLATE, ETHYLHEXYLGLYCERIN, HYDROXYPROPYL CYCLODEXTRIN, ETHYL LINALOOL, TRIETHANOLAMINE, CYCLAMEN ALDEHYDE, GAMMA-UNDECALACTONE, METHYLENEDIOXYPHENYL METHYLPROPANAL, CITRONELLYL ACETATE, METHYL DIMETHYLMETHYLENECYCLOHEXANE CARBOXYLATE, CITRIC ACID, SODIUM BENZOATE, IODOPROPYNYL BUTYLCARBAMATE, PHENOXYETHANOL.

  • Principal Display Panel - 50 mL carton

    mary kay

    BOTANICAL EFFECTS

    UVA

    HIGH PROTECTION

    MOISTURIZING LOTION WITH SPF 30

    50 mL

    image of EU/LATAM carton

  • INGREDIENTS AND APPEARANCE
    BOTANICAL EFFECTS MOISTURIZER SPF 30 
    avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51531-4850
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE9 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE2.75 g  in 100 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE4.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    HYLOCEREUS UNDATUS FRUIT (UNII: WUG58TD53X)  
    2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HYDROXYPROPYL .ALPHA.-CYCLODEXTRIN (UNII: ZFR0T80O4Y)  
    ETHYL LINALOOL (UNII: SF2JS9GF5T)  
    BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    CYCLAMEN ALDEHYDE (UNII: 4U37UX0E1E)  
    .GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL)  
    3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA)  
    CITRONELLYL ACETATE (UNII: IZ420RT3OY)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51531-4850-71 in 1 CARTON08/21/2014
    150 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only08/21/2014
    Labeler - Mary Kay Inc. (049994452)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mary Kay Inc.103978839manufacture(51531-4850)
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