Label: EUCERIN AGE DEFENSE SPF 50 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene lotion

  • NDC Code(s): 66800-5000-3, 66800-5000-4
  • Packager: Beiersdort Inc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 27, 2024

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  • Drug Facts

  • Active ingredients

    Avobenzone, Homosalate, Octisalate, Octocrylene

  • 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

    Do not use on damaged or broken skin

  • WHEN USING

    When using this product keep out of eyes. Rinse with water to remove.

  • KEEP OUT OF REACH OF CHILDREN

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

  • STOP USE

    Stop use and ask a doctor if rash occurs

  • Directions

    ■ 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-sleeve shirts, pants, hats, and sunglasses

    ■ children under 6 months: Ask a doctor

  • Other information

    ■ protect this product from excessive heat and direct sun

    ■ may stain or damage some fabrics or surfaces

    ■ store this product in upright position

  • Inactive ingredients

    Water, Alcohol Denat., Butyloctyl Salicylate, Silica, C12-15 Alkyl Benzoate, Polyglyceryl-6 Stearate, Sodium Stearoyl Glutamate, Diisostearoyl Polyglyceryl-3 Dimer Dilinoleate, Behenyl Alcohol, Butylene Glycol Dicaprylate/Dicaprate, Cetearyl Alcohol, Copernicia Cerifera (Carnauba) Wax, Dibutyl Adipate, Sodium Hyaluronate, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Tocopherol, Dimethicone, Silica Dimethyl Silylate, Diethylhexyl Syringylidenemalonate, Ethylcellulose, Glyceryl Behenate, L-Carnitine, Polyglyceryl-6 Octastearate, Phenoxyethanol, Glycerin, Xanthan Gum, Ethylhexylglycerin, Disodium EDTA, Hydroxyacetophenone, Polyglyceryl-6 Behenate, Cetyl Alcohol, Sodium Ascorbyl Phosphate

  • Questions?

    1-800-227-4703

  • PRINCIPAL DISPLAY PANEL

    Eucerin ®

    Age Defense

    +Hyaluronic Acid

    Lightweight Sunscreen Lotion For Face

    50 Broad Spectrum SPF 50

    Helps Reduce The Signs of Aging*

    Hypoallergenic | Fragrance Free

    No Oxybenzone & Octinoxate

    5 AOX Shield

    Antioxidant Defense

    Developed with Dermatologists

    2.5 FL OZ (75 mL)

    Eucerin Age Defense

  • INGREDIENTS AND APPEARANCE
    EUCERIN AGE DEFENSE SPF 50 SUNSCREEN 
    avobenzone, homosalate, octisalate, octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66800-5000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE10 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCINE PROPIONYL-L-CARNITINE (UNII: 8KVN59D5FL)  
    POLYGLYCERYL-6 DISTEARATE (UNII: Z35I17EQOP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
    ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    WATER (UNII: 059QF0KO0R)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ENOXOLONE (UNII: P540XA09DR)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)  
    GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    POLYGLYCERYL-6 STEARATE (UNII: ETY9Q81E2T)  
    DIISOSTEAROYL POLYGLYCERYL-3 DIMER DILINOLEATE (UNII: G3232Z5S2O)  
    DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
    POLYGLYCERYL-6 BEHENATE (UNII: 4T2L7QI313)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
    ALCOHOL (UNII: 3K9958V90M)  
    DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    COPERNICIA PRUNIFERA WHOLE (UNII: 6EKZ38572S)  
    DIBUTYL ADIPATE (UNII: F4K100DXP3)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    Product Characteristics
    Colorwhite (Off-White to Yellow) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66800-5000-475 g in 1 TUBE; Type 0: Not a Combination Product11/03/2021
    2NDC:66800-5000-310 g in 1 POUCH; Type 0: Not a Combination Product11/07/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/03/2021
    Labeler - Beiersdort Inc (001177906)
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