Label: ETHICAL ZINC DAILY WEAR LIGHT SUNSCREEN SPF-50- zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 25, 2023

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  • ACTIVE INGREDIENTS

    ZINC OXIDE 22.70%

  • PURPOSE

    SUNSCREEN

  • USE

    • HELPS PREVENT SUNBURN.
    • IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS) DECREASES THE RISK OF CANCER AND EARLY SKIN AGING CAUSED BY THE 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.

    STOP USE AND ASK A DOCTOR IF

    • RASH OCCURS.
  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

  • DIRECTIONS

    • APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.

    REAPPLY:

    • AFTER 80 MINUTES OF SWIMMING OR SWEATING
    • IMMEDIATELY AFTER TOWEL DRYING
    • AT LEAST EVERY 2 HOURS
    • CHILDREN UNDER 6 MONTHS: ASK A DOCTOR.
  • INACTIVE INGREDIENTS

    PURIFIED WATER, COCO CAPRYLATE/CAPRATE, MEDIUM CHAIN TRIGLYCERIDES, OCTYLDODECANOL, GLYCEROL, CETEARYL ALCOHOL, POLYGLYCERYL-3 POLYRICINOLEATE, PEG-30 DIPOLYHYDROXYSTEARATE, GLUCONOLACTONE, ISOSTEARIC ACID, SODIUM CHLORIDE, SODIUM BENZOATE, CETEARYL GLUCOSIDE, EDTA, XANTHAN GUM.

  • OTHER INFORMATION

    • PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUN.
  • PRINCIPAL DISPLAY PANEL

    01b LBL_Daily Wear Light Sunscreen SPF-50_100g

  • INGREDIENTS AND APPEARANCE
    ETHICAL ZINC DAILY WEAR LIGHT SUNSCREEN   SPF-50
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72962-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION22.7 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)  
    PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    ISOSTEARIC ACID (UNII: X33R8U0062)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72962-102-11100 g in 1 TUBE; Type 0: Not a Combination Product12/12/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35212/12/2020
    Labeler - ETHICAL ZINC PTY LTD (745184258)
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