Label: ANTI-AGING DAY SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, octinoxate, octisalate, octocrylene cream

  • NDC Code(s): 68026-503-01, 68026-503-05, 68026-503-07, 68026-503-15, view more
    68026-503-50
  • Packager: La Prairie, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 September 20, 2018

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

  • Active Ingredients

    Avobenzone 3.0%
    Octinoxate 7.5%
    Octisalate 5.0%
    Octocrylene 2.5%

    Purpose

    Sunscreen

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  • Uses

    • helps prevent sunburn

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  • Warnings

    For external use only

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  • Do not use

    on damaged or broken skin

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  • When using this product

    keep out of eyes. Rinse with water to remove.

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  • Stop use and ask a doctor if

    rash occurs

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  • 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 after cleansing and toning • smooth over face and throat • 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 increase 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), C12-15 Alkyl Ethylhexanoate, Glycerin, Dimethicone/Vinyl Dimethicone Crosspolymer, Polyglyceryl-3 Methylglucose Distearate, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Steareth-21, Behenyl Alcohol, Butylene Glycol, Glycoproteins*, Panax Ginseng Root Extract*, Equisetum Arvense Extract*, Sodium Hyaluronate, Caprooyl Tetrapeptide-3, Salicornia Herbacea Extract, Sodium PCA, Triacetin, Tocopheryl Acetate, Resveratrol, Lactobacillus Ferment, Acetyl Decapeptide-3, Trehalose, Urea, Larix Sibirica Wood Extract, Palmitoyl Tripeptide-8, Carnosine, Potato Starch Modified, Disodium EDTA , Myrothamnus Flabellifolia Leaf Extract, Kefiran, Sodium Hydroxide, Glyceryl Stearate, Chlorella Vulgaris Extract, Silica, Panthenol, Polyquaternium-51, Glycine Soja (Soybean) Oil, PEG-100 Stearate, Hydrogenated Lecithin, Allantoin, Hydroxyethyl Behenamidopropyl Dimonium Chloride, C13-14 Isoparaffin, Dextran, Caprylic/Capric Triglyceride, Polysorbate 80, Sodium Oleate, Laureth-7, Saccharomyces Cerevisiae Extract, Cetyl Dimethicone, Caprylyl Glycol, Polyquaternium-67, Steareth-2, Polyacrylamide, Carbomer, Synthetic Wax, Alcohol, Fragrance (Parfum), Linalool, Hexyl Cinnamal, Hydroxycitronellal, Alpha-Isomethyl Ionone, Geraniol, Citronellol, Benzyl Benzoate, Butylphenyl Methylpropional, Evernia Furfuracea (Treemoss) Extract, Eugenol, Benzyl Salicylate, Ethylhexylglycerin, Phenoxyethanol, Sorbic Acid, Sodium Dehydroacetate, Chlorphenesin, Methylparaben, Benzoic Acid, Yellow 5 (CI 19140), Red 4 (CI 14700) i73 * La Prairie’s exclusive Cellular Complex US Patent 5,840,309

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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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  • LABORATOIRES LA PRAIRIE S.A.

    CLARENS/MONTREUX • ZURICH D-76530 BADEN-BADEN MILANO • PARIS LA PRAIRIE, INC., DISTR. NEW YORK, N.Y. 10019

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  • PRINCIPAL DISPLAY PANEL

    ANTI-AGING DAY CREAM SUNSCREEN BROAD SPECTRUM CREME DE JOUR ANTI-AGE CREME SOLAIRE LARGE SPECTRE SPF 30 la prairie SWITZERLAND 50 ml e / NET WT. 1.7 OZ. MADE IN SWITZERLAND

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  • Product Labels
  • INGREDIENTS AND APPEARANCE
    ANTI-AGING DAY SUNSCREEN BROAD SPECTRUM SPF 30 
    avobenzone, octinoxate, octisalate, octocrylene cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68026-503
    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
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 25 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    C12-15 ALKYL ETHYLHEXANOATE (UNII: GQJ580CH83)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    STEARETH-21 (UNII: 53J3F32P58)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CAPROOYL TETRAPEPTIDE-3 (UNII: LZI0HJ3K2R)  
    SALICORNIA EUROPAEA (UNII: 6ADL50JAKW)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    TRIACETIN (UNII: XHX3C3X673)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    RESVERATROL (UNII: Q369O8926L)  
    LACTOBACILLUS REUTERI (UNII: 9913I24QEE)  
    ACETYL DECAPEPTIDE-3 (UNII: 30510A08G7)  
    TREHALOSE (UNII: B8WCK70T7I)  
    UREA (UNII: 8W8T17847W)  
    LARIX SIBIRICA WOOD (UNII: KSC3PGF73L)  
    CARNOSINE (UNII: 8HO6PVN24W)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    MYROTHAMNUS FLABELLIFOLIA LEAF (UNII: 6Y9E0R40J5)  
    KEFIRAN (UNII: 8L821V6V99)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    ALLANTOIN (UNII: 344S277G0Z)  
    HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM OLEATE (UNII: 399SL044HN)  
    LAURETH-7 (UNII: Z95S6G8201)  
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    STEARETH-2 (UNII: V56DFE46J5)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    ALCOHOL (UNII: 3K9958V90M)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    GERANIOL (UNII: L837108USY)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
    PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)  
    EUGENOL (UNII: 3T8H1794QW)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SORBIC ACID (UNII: X045WJ989B)  
    SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68026-503-50 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2017 12/31/2021
    2 NDC:68026-503-05 5 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2017 12/31/2021
    3 NDC:68026-503-01 1 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2017 12/31/2021
    4 NDC:68026-503-07 7 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2017 12/31/2021
    5 NDC:68026-503-15 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2017 12/31/2021
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 10/22/2013 12/31/2021
    Labeler - La Prairie, Inc. (606554996)
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