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
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ACTIVE INGREDIENTActive ingredients purpose - Octinoxate 7.5% Sunscreen - Zinc Oxide 10.8 Sunscreen
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PURPOSEUses: 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.
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KEEP OUT OF REACH OF CHILDRENKeep out of reach of children. If swallowed, get help or contact a Poison Control Center right away.
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INDICATIONS & USAGEStop use and ask a doctor if rash occurs
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WARNINGSWarnings: For external use only. Avoid contact with eyes. Rinse with water to remove. Do not use on damaged or broken skin.
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DOSAGE & ADMINISTRATIONDirections: 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 ...
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INACTIVE INGREDIENTInactive ingredients: Water, Polysorbate 60, Coconut Alkanes, C12-15 Alkyl Benzoate, Octyldodecanol Neopentanoate, Glycerin, Cetearyl Alcohol, Cyclopentasiloxane, Glyceryl Stearate, PEG-100 ...
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PRINCIPAL DISPLAY PANELVitality Institute - SPF 50 Daily UV Defense Broad Spectrum Sunscreen - 2 Fl Oz / 59 mL
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INGREDIENTS AND APPEARANCEProduct Information