Label: SUNSCREEN- zinc oxide emulsion

  • NDC Code(s): 35192-050-17
  • Packager: CA-Botana International
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 18, 2025

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  • Active Ingredient
    Zinc Oxide 21%............................................. Sunscreen
  • Purpose
    Sunscreen
  • Ask Doctor
    Stop use and ask a doctor if rash occurs
  • Keep out of reach of children
    Keep out of reach of children
  • Inactive Ingredients
    Water (Aqua), Coco-Caprylate/Caprate, Ceteary Alcohol, Propanediol, Stearyl Alcohol, Polyhydroxystearic Acid, Mica, Cetearyl Olivate, Sorbitan Olivate, Caprylhydroxamic acid ...
  • Safety information
    Protect this product from excessive heat and direct sun
  • Dosage & Administration
    Helps prevent sunburn. If used as directed with other sun protection measured decreases the risk of skin cancer and early skin aging caused by the sun. Apply liberally 15 minutes before 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. If product is swallowed get medical help or contact a poison ...
  • Indications & Usage
    Apply liberally 15 minutes before exposure, use water resistant sunscreen, if swimming or sweating. reapply at least every 2 hours. Children under 6 months: ask a doctor
  • PRINCIPAL DISPLAY PANEL
    2025-4_5008_elixir mineral sunscreen SPF 50
  • INGREDIENTS AND APPEARANCE
    Product Information