Label: SUNPLUS SPF50 FACE BODY SUNSCREEN- sunscreen lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 13, 2024

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  • ACTIVE INGREDIENT

    Homosalate- 15%

    Octocrylene- 6%

    Octisalate- 5%

    Avobenzone- 2%

  • PURPOSE

    Sunscreen

  • KEEP OUT OF REACH OF CHILDREN

    WARNING - Keep out of reach of children

  • INDICATIONS & USAGE

    Helps prevent sunburn and photodamage.

    If used as directed with other sun protection measures, decreases the risk of skin cancer and early aging caused by the sun.

  • INACTIVE INGREDIENT

    Purified Water, Glycerin, Ceteareth-20, Cetearyl Alcohol, Dimethicone, Glyceryl stearate, PEG-100, Acrylic Polymer, Cetyl Alcohol, Potassium Hexadecyl Phosphate, PEG 300, Grapeseed Oil, Sunflower Oil, Safflower Oil, Organic Borage Oil, Organic Evening Primrose Oil, Allantoin, Hyaluronic Acid, Organic Raspberry Seed Oil, Organic Jojoba Oil, Organic Aloe Oil, Phenoxyethanol, Ethylhexylglycerin

  • WARNINGS

    For external use only. Do not use on damaged or broken skin. When using this product keep out f eyes. Rinse with water to remove. Stop use and ask a doctor if rash or irritation occurs. If swallowed get medical help or contact Poison Control Center. Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Apply liberally to dry skin 15 minutes before sun exposure. Reapply to dry skin after 80 minutes of swimming or sweating, immediately after towel drying, at least every 2 hours. Children under 6 months ask a doctor.

  • PRINCIPAL DISPLAY PANEL

    Sunplus SPF 50

  • INGREDIENTS AND APPEARANCE
    SUNPLUS SPF50 FACE BODY SUNSCREEN 
    sunscreen lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65112-304
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE0.06 g  in 118 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE0.05 g  in 118 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE0.15 g  in 118 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE0.02 g  in 118 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65112-304-01118 mL in 1 TUBE; Type 0: Not a Combination Product06/01/2004
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/01/2004
    Labeler - I.Shay Cosmetics (151582384)
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