Label: ANTI-AGING EYE SUNSCREEN BROAD SPECTRUM SPF 15  - avobenzone, octinoxate and octisalate cream 

  • Label RSS
  • NDC Code(s): 68026-501-03, 68026-501-15
  • Packager: La Prairie, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 10/13

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  • ANTI-AGING EYE CREAM SUNSCREEN BROAD SPECTRUM SPF 15
  • Active Ingredients

    Avobenzone 2.0%
    Octinoxate 7.5%
    Octisalate 3.0%

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  • Purpose

    Sunscreen

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  • Uses

    • helps prevent sunburn
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  • 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.


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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

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  • Directions

    • apply daily under the eye and along the brow line
    • apply liberally 15 minutes before sun exposure
    • children under 6 months of age: Ask a doctor
    • 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-sleeve shirts, pants, hats, and sunglasses
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  • Inactive Ingredients

    Water (Aqua), Cetearyl Alcohol, Soybean Glycerides, Butyrospermum Parkii (Shea Butter) Unsaponifiables, Polyethylene, Myristyl Myristate, Ethoxydiglycol, Butylene Glycol, Synthetic Beeswax, Glyceryl Caprylate, Glycoproteins*,
    Panax Ginseng Root Extract*, Equisetum Arvense (Horsetail) Extract*, Hesperetin Laurate,  Saccharomyces/Xylinum/Black Tea Ferment, Tocopherol, Hydrolyzed Malt Extract, Lecithin, Olea Europaea (Olive) Oil Unsaponifiables, Ursolic Acid, Erythrityl Triethylhexanoate, Plankton Extract, Ilomastat, Carnosine, Echium Plantagineum Seed Oil, Carbomer, Caprylyl/Capryl Glucoside, Serine, Silybum Marianum Fruit Extract, Acacia Senegal Gum, Ascorbyl Tetraisopalmitate, Triticum Vulgare (Wheat) Germ Oil Unsaponifiables, Hydroxyethylcellulose, Lauroyl Lysine, Melissa Officinalis Leaf Extract, PEG-8, Pollen Extract, Hydrogenated Lecithin, Glycerin, Trehalose, Glycine Soja (Soybean) Oil Unsaponifiables, Polyquaternium-51, Sodium Hyaluronate, Camellia Sinensis Leaf Extract, Sodium Acrylate/ Sodium Acryloyldimethyl Taurate Copolymer, PEG-6 Isostearate, Propylene Glycol, Cyclopentasiloxane, Caprylic/Capric Triglyceride, Urea, Sodium PCA, Isodecyl Salicylate, Tocopheryl Linoleate/Oleate, Algin, Disodium EDTA, Isopropylbenzyl Salicylate, Steareth-2, Phospholipids, DNA, Polyisobutene, Ceteth-20, Xanthan Gum, Triacetin, Mica, Cyclomethicone, Polymethyl Methacrylate, Steareth-21, Cyclohexasiloxane, Sucrose, Stearic Acid, Alcohol, Aluminum Hydroxide, Fragrance (Parfum), Benzyl Alcohol, Linalool, Hydroxycitronellal, Alpha-Isomethyl Ionone, Amyl Cinnamal, Hexyl Cinnamal, Evernia Furfuracea (Treemoss) Extract, Geraniol, Benzyl Benzoate, Butylphenyl Methylpropional, Phenoxyethanol, Benzoic Acid, Methylparaben, Potassium Sorbate, Chlorphenesin, Ethylparaben, Butylparaben, Propylparaben, Isobutylparaben, Titanium Dioxide (CI 77891)

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  • Other Information

    • Protect the product in this container from excessive heat and direct sun
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  • Questions or Comments?

    • Call toll free 1-800-821-5718 or visit www.laprairie.com
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  • ANTI-AGING EYE CREAM SUNCREEN BROAD SPECTRUM SPF 15 15ml (68026-501-15) | ANTI-AGING EYE CREAM SUNCREEN BROAD SPECTRUM SPF 15 3ml (68026-501-03)
  • INGREDIENTS AND APPEARANCE
    ANTI-AGING EYE SUNSCREEN BROAD SPECTRUM SPF 15  
    avobenzone, octinoxate, octisalate cream
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:68026-501
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AVOBENZONE (AVOBENZONE) AVOBENZONE 20 mg  in 1 mL
    OCTINOXATE (OCTINOXATE) OCTINOXATE 75 mg  in 1 mL
    OCTISALATE (OCTISALATE) OCTISALATE 30 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    CETOSTEARYL ALCOHOL  
    SHEANUT OIL  
    MYRISTYL MYRISTATE  
    DIETHYLENE GLYCOL MONOETHYL ETHER  
    BUTYLENE GLYCOL  
    GLYCERYL CAPRYLATE  
    EQUISETUM ARVENSE TOP  
    ALPHA-TOCOPHEROL  
    URSOLIC ACID  
    ILOMASTAT  
    CARNOSINE  
    ECHIUM PLANTAGINEUM SEED OIL  
    CAPRYLYL GLYCOL  
    SERINE  
    SILYBUM MARIANUM SEED  
    ACACIA  
    WHEAT GERM OIL  
    HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)  
    LAUROYL LYSINE  
    MELISSA OFFICINALIS LEAF  
    POLYETHYLENE GLYCOL 400  
    GLYCERIN  
    TREHALOSE  
    SOYBEAN OIL  
    HYALURONATE SODIUM  
    GREEN TEA LEAF  
    CYCLOMETHICONE 5  
    UREA  
    SODIUM PYRROLIDONE CARBOXYLATE  
    SODIUM ALGINATE  
    EDETATE DISODIUM  
    STEARETH-2  
    HERRING SPERM DNA  
    POLYISOBUTYLENE (1200000 MW)  
    CETETH-20  
    MICA  
    CYCLOMETHICONE  
    STEARETH-21  
    CYCLOMETHICONE 6  
    STEARIC ACID  
    ALCOHOL  
    ALUMINUM HYDROXIDE  
    BENZYL ALCOHOL  
    LINALOOL, DL-  
    HYDROXYCITRONELLAL  
    ISOMETHYL-.ALPHA.-IONONE  
    .ALPHA.-HEXYLCINNAMALDEHYDE  
    PSEUDEVERNIA FURFURACEA  
    GERANIOL  
    BENZYL BENZOATE  
    BUTYLPHENYL METHYLPROPIONAL  
    PHENOXYETHANOL  
    BENZOIC ACID  
    METHYLPARABEN  
    POTASSIUM SORBATE  
    CHLORPHENESIN  
    ETHYLPARABEN  
    BUTYLPARABEN  
    PROPYLPARABEN  
    ISOBUTYLPARABEN  
    TITANIUM DIOXIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68026-501-15 15 mL in 1 BOTTLE
    2 NDC:68026-501-03 3 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part352 04/12/2011
    Labeler - La Prairie, Inc. (092848621)
    Establishment
    Name Address ID/FEI Business Operations
    Trichema Ag 480006600 manufacture(68026-501)
    Establishment
    Name Address ID/FEI Business Operations
    Frike Cosmetic AG 485853761 manufacture(68026-501)
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