Label: EUCERIN DAILY PROTECTION BODY - avobenzone, homosalate and octisalate lotion 

  • NDC Code(s): 10356-326-03, 10356-326-07, 10356-326-31, 10356-326-36
  • Packager: Beiersdorf Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 07/13

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

  • ACTIVE INGREDIENT

    Active Ingredients                  
    Avobenzone 2.7%
    Homosalate 9.0%
    Octisalate 4.5%

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  • WARNINGS

    Warnings
    For external use only

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  • DO NOT USE

    Do not use on damaged or broken skin.

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  • WHEN USING

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

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  • STOP USE

    Stop use and ask a doctor if irritation occurs.

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  • 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.

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  • 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.

    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
    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

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  • QUESTIONS

    Questions or comments?
    1-800-227-4703


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  • INACTIVE INGREDIENT

    Inactive ingredients
    Water, Glycerin, Diethylhexyl 2,6-Naphthalate, Cetearyl Alcohol, Dimethicone,
    Glyceryl Stearate SE, Tocopheryl Acetate, Synthetic Beeswax, Chondrus
    Crispus (Carrageenan), Peg-40 Castor Oil, 1,2-Hexanediol, Sodium
    Polyacrylate, Caprylyl Glycol, Silica Dimethyl Silyate, Sodium Cetearyl
    Sulfate, Trisodium EDTA, Phenoxyethanol, Piroctone Olamine, Disodium EDTA.

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  • PRINCIPAL DISPLAY PANEL

    EUCERIN

    Daily Protection
    Moisturizing Body Lotion

    Broad Spectrum SPF 15
    Sunscreen

    Moisturizes and helps protect skin
    from sun burn and long term sun damage

    Fragrance free

    eucerindailyprotectionlotionbsfronteucerindailyprotectionlotionbsback



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  • INGREDIENTS AND APPEARANCE
    EUCERIN DAILY PROTECTION BODY 
    avobenzone, homosalate, octisalate lotion
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:10356-326
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AVOBENZONE (AVOBENZONE) AVOBENZONE 2.7 g  in 100 mL
    HOMOSALATE (HOMOSALATE) HOMOSALATE 9 g  in 100 mL
    OCTISALATE (OCTISALATE) OCTISALATE 4.5 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    GLYCERIN  
    DIETHYLHEXYL 2,6-NAPHTHALATE  
    CETOSTEARYL ALCOHOL  
    DIMETHICONE  
    GLYCERYL STEARATE SE  
    YELLOW WAX  
    CHONDRUS CRISPUS  
    PEG-40 CASTOR OIL  
    ALPHA-TOCOPHEROL ACETATE  
    1,2-HEXANEDIOL  
    SODIUM POLYACRYLATE (8000 MW)  
    EDETATE TRISODIUM  
    PHENOXYETHANOL  
    CAPRYLYL GLYCOL  
    PIROCTONE OLAMINE  
    SODIUM CETOSTEARYL SULFATE  
    EDETATE DISODIUM  
    SILICA DIMETHYL SILYLATE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10356-326-31 500 mL in 1 BOTTLE, PUMP
    2 NDC:10356-326-36 625 mL in 1 BOTTLE, PUMP
    3 NDC:10356-326-03 14 mL in 1 BOTTLE
    4 NDC:10356-326-07 59 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 07/15/2013
    Labeler - Beiersdorf Inc (001177906)
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