Label: EUCERIN REDNESS RELIEF DAILY PERFECTING- avobenzone, homosalate, octisalate, octocrylene lotion

  • NDC Code(s): 10356-353-05, 10356-353-32
  • Packager: Beiersdorf Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 29, 2023

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

  • ACTIVE INGREDIENT

    Active ingredients

    Avobenzone 2.0%

    Homosalate 3.5%

    Octisalate 3.5%

    Octocrylene 4.5%

  • PURPOSE

    Purpose

    Sunscreen

  • INDICATIONS & USAGE

    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

    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.

  • STOP USE

    Stop use and ask a doctor if rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Directions For sunscreen use:

    • apply liberally 15 minutes before sun exposure

    • use a water resistant sunscreen if swimming or sweating

    • reapply at least every 2 hours

    • children under 6 months of age: Ask a doctor

    • 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.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Glycerin, Methylpropanediol, Titanium Dioxide,

    Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol,

    Pentylene Glycol, Dimethicone, Glycyrrhiza Inflata Root

    Extract, Potassium Cetyl Phosphate, Caprylyl Glycol,

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer,

    Xanthan Gum, Phenoxyethanol, Chromium Oxide

    Greens, Sodium Hydroxide, Trisodium EDTA.

  • PRINCIPAL DISPLAY PANEL

    Eucerin

    REDNESS RELIEF

    DAY LOTION

    Broad Spectrum SPF 15

    Sunscreen

    Subtle Green Color Neutralizers

    immediately reduce visible redness and blotchiness

    Fragrance-free, Paraben Free

    Dermatological skincare

    eucredreliefcarton

  • INGREDIENTS AND APPEARANCE
    EUCERIN REDNESS RELIEF DAILY PERFECTING 
    avobenzone, homosalate, octisalate, octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10356-353
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE4.5 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE3.5 g  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE3.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    EDETATE TRISODIUM (UNII: 420IP921MB)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CHROMIC OXIDE (UNII: X5Z09SU859)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10356-353-0550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/30/2017
    2NDC:10356-353-321.5 mL in 1 PACKET; Type 0: Not a Combination Product03/30/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/30/2017
    Labeler - Beiersdorf Inc (001177906)