Label: KIEHLS SINCE 1851 SUPER MULTI CORRECTIVE BROAD SPECTRUM SPF 30 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene cream

  • NDC Code(s): 49967-410-01, 49967-410-02, 49967-410-03, 49967-410-04
  • Packager: L’Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2024

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  • Active ingredient

    Avobenzone 3%

    Homosalate 5%

    Octisalate 5%

    Octocrylene 7%

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

  • Directions

    For sunscreen use:

    • apply liberally 15 minutes before sun exposure
    • reapply at least every 2 hours
    • use a water resistant sunscreen if swimming or sweating
    • 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 value 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-sleeved shirts, pants, hats, and sunglasses

    • 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, glyceryl stearate, hydroxypropyl tetrahydropyrantriol, silica, PEG-100 stearate, propylene glycol, euphorbia cerifera (candelilla) wax, phenoxyethanol, ammonium polyacryloyldimethyl taurate, stearic acid, dicaprylyl carbonate, cetyl alcohol, palmitic acid, capryloyl salicylic acid, caprylyl glycol, xanthan gum, dimethicone/vinyl dimethicone crosspolymer, fragrance, disodium EDTA, tocopherol, sodium hyaluronate, adenosine, linalool, sodium hydroxide, jasminum officinale (jasmine) flower extract, citronellol, geraniol, citral, benzyl alcohol, citric acid

  • Questions or comments?

    Call toll free 1-800-946-4453

    Monday - Friday (9 a.m. to 5 p.m. EST)

  • PRINCIPAL DISPLAY PANEL

    image of a label

    image of a label
  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 SUPER MULTI CORRECTIVE BROAD SPECTRUM SPF 30 SUNSCREEN 
    avobenzone, homosalate, octisalate and octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-410
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE50 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    HYDROXYPROPYL TETRAHYDROPYRANTRIOL (UNII: 4U3GMG1OT1)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ADENOSINE (UNII: K72T3FS567)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)  
    .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)  
    GERANIOL (UNII: L837108USY)  
    CITRAL (UNII: T7EU0O9VPP)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-410-0150 mL in 1 JAR; Type 0: Not a Combination Product07/01/2015
    2NDC:49967-410-02125 mL in 1 JAR; Type 0: Not a Combination Product07/01/2015
    3NDC:49967-410-0375 mL in 1 JAR; Type 0: Not a Combination Product07/01/2015
    4NDC:49967-410-043 mL in 1 PACKET; Type 0: Not a Combination Product07/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02007/01/2015
    Labeler - L’Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L’Oreal USA, Inc.185931458manufacture(49967-410)
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