Label: EUCERIN SENSITIVE MINERAL FACE SUNSCREEN SPF 35- zinc oxide 24% lotion

  • NDC Code(s): 66800-7000-1, 66800-7000-5
  • Packager: Beiersdorf 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 March 3, 2023

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  • Drug Facts

  • Active ingredient

    Zinc Oxide 24%

  • 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 on damaged or broken skin
    When using this product keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctor if rash occurs

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

  • 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, C12-15 Alkyl Benzoate, Isopropyl Palmitate, Butyloctyl Salicylate, Ethylhexyl Pelargonate, Cetyl PEG/PPG-10/1 Dimethicone, Propylene Glycol, Cyclopentasiloxane, Bis-Octyldodecyl Dimer Dilinoleate/Propanediol Copolymer, Dimethicone, Diethylhexyl Syringylidenemalonate, Ethylhexyl Methoxycrylene, Polyester-27, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Sodium Ascorbyl Phosphate, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopherol (Vitamin E), Triethoxycaprylylsilane, Beeswax, Hydroxyacetophenone, Sodium Chloride, PEG-12 Dimethicone Crosspolymer, 1,2-Hexanediol, Caprylyl Glycol, Jojoba Esters, Silica, Polyglyceryl-6 Polyricinoleate, Iron Oxides

  • Questions?

    1-800-227-4703

  • PRINCIPAL DISPLAY PANEL

    Eucerin ®

    Sensitive Mineral Face

    Zinc Oxide Protection

    Tinted Sunscreen Lotion For Face

    35

    Broad Spectrum SPF 35

    Blendable Tint For All Skin Tones

    5 AOX Shield™

    Antioxidant Defense

    Developed With Dermatologists

    Sens Mineral Face Front

    Sens Mineral Face Rear

  • INGREDIENTS AND APPEARANCE
    EUCERIN SENSITIVE MINERAL FACE SUNSCREEN SPF 35 
    zinc oxide 24% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66800-7000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE24 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)  
    SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BIS-OCTYLDODECYL DIMER DILINOLEATE/PROPANEDIOL COPOLYMER (UNII: TY3J98ZR7R)  
    JOJOBA OIL (UNII: 724GKU717M)  
    WATER (UNII: 059QF0KO0R)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
    PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    ETHYLHEXYL PELARGONATE (UNII: 3YU1SQ04DV)  
    DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
    ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
    POLYESTER-7 (UNII: 0841698D2F)  
    FERROUS OXIDE (UNII: G7036X8B5H)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)  
    ENOXOLONE (UNII: P540XA09DR)  
    Product Characteristics
    Colorwhite ((off-white to yellow)) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66800-7000-51 in 1 CARTON01/01/2023
    150 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:66800-7000-110 g in 1 POUCH; Type 0: Not a Combination Product03/03/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35201/01/2023
    Labeler - Beiersdorf Inc (001177906)
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