Home > Drugs A-Z > Kiehls Since 1851 Activated Sun Protector for Face Broad Spectrum SPF 50 Sunscreen

Kiehls Since 1851 Activated Sun Protector for Face Broad Spectrum SPF 50 Sunscreen (L'Oreal USA Products Inc)

Available Formats

Dosage Form Package Information Links
LOTION 100 mL in 1 BOTTLE, PLASTIC (49967-631-01) Label Information

Complete Kiehls Since 1851 Activated Sun Protector for Face Broad Spectrum SPF 50 Sunscreen Information

  • Active ingredients

    Avobenzone 3%

    Homosalate 15%

    Octisalate 5%

    Octocrylene 5%

    Oxybenzone 6%


  • 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 Poision Control Center right away.


  • Directions

    For sunscreen use:

    ● apply liberally 15 minutes before sun exposure

    ● reapply:

      ● after 80 minutes of swimming or sweating

      ● immediately after towel drying

      ● 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 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, dimethicone, isododecane, styrene/acrylates copolymer, propanediol, glycerin, silica, isononyl isononanoate, inulin lauryl carbamate, nylon-12, caprylyl methicone, synthetic wax, poly C10-30 alkyl acrylate, phenoxyethanol, lycium barbarum fruit extract, sucrose tristearate, ammonium acryloyldimethyltaurate/steareth-25 methacrylate crosspolymer, PEG-8 laurate, stearyl alcohol, polymethyl methacrylate, p-anisic acid, chlorphenesin, dimethiconol, xanthan gum, disodium EDTA, tocopherol, triethanolamine, hydrolyzed triticum monococcum seed extract


  • Questions or comments?

    Call toll free 1-800-946-4453


  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 ACTIVATED SUN PROTECTOR FOR FACE BROAD SPECTRUM SPF 50 SUNSCREEN 
    avobenzone, homosalate, octisalate, octocrylene and oxybenzone lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-631
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 60 mg  in 1 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49967-631-01 100 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 06/01/2013
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    Name Address ID/FEI Business Operations
    Dimensional Merchandising Inc. 076693183 manufacture(49967-631)