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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- Official Label (Printer Friendly)
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Active IngredientZinc Oxide 21%............................................. Sunscreen
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PurposeSunscreen
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Ask DoctorStop use and ask a doctor if rash occurs
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Keep out of reach of childrenKeep out of reach of children
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Inactive IngredientsWater (Aqua), Coco-Caprylate/Caprate, Ceteary Alcohol, Propanediol, Stearyl Alcohol, Polyhydroxystearic Acid, Mica, Cetearyl Olivate, Sorbitan Olivate, Caprylhydroxamic acid ...
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Safety informationProtect this product from excessive heat and direct sun
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Dosage & AdministrationHelps 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 ...
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WarningsFor 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 ...
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Indications & UsageApply 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
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information