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
  • DEA Schedule: None

Drug Label Information

Updated November 7, 2023

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

  • 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)