Label: SPF 50 DAILY UV DEFENSE BROAD SPECTRUM SUNSCREEN- octinoxate, zinc oxide cream

  • NDC Code(s): 70484-008-01, 70484-008-02, 70484-008-03, 70484-008-04
  • Packager: Vi Medical Products, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 20, 2025

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

  • ACTIVE INGREDIENT
    Active ingredients purpose - Octinoxate 7.5% Sunscreen - Zinc Oxide 10.8 Sunscreen
  • PURPOSE
    Uses: Helps prevent sunburn if used as directed with other sun protection ( see directions), decreases the risk of skin cancer and early skin aging caused by the sun.
  • KEEP OUT OF REACH OF CHILDREN
    Keep out of reach of children. If swallowed, get help or contact a Poison Control Center right away.
  • INDICATIONS & USAGE
    Stop use and ask a doctor if rash occurs
  • WARNINGS
    Warnings: For external use only. Avoid contact with eyes. Rinse with water to remove. Do not use on damaged or broken skin.
  • DOSAGE & ADMINISTRATION
    Directions: Apply liberally and evenly 15 minutes before sun exposure. Reapply as needed or after towel drying, swimming, or sweating. Sun Protection Measures: Spending time in the sun ...
  • INACTIVE INGREDIENT
    Inactive ingredients: Water, Polysorbate 60, Coconut Alkanes, C12-15 Alkyl Benzoate, Octyldodecanol Neopentanoate, Glycerin, Cetearyl Alcohol, Cyclopentasiloxane, Glyceryl Stearate, PEG-100 ...
  • PRINCIPAL DISPLAY PANEL
    Vitality Institute - SPF 50 Daily UV Defense Broad Spectrum Sunscreen - 2 Fl Oz / 59 mL
  • INGREDIENTS AND APPEARANCE
    Product Information