Label: DAILY DEFLECTOR MINERAL SUNSCREEN SPF 40- zinc oxide lotion

  • NDC Code(s): 43479-209-11, 43479-209-12, 43479-209-52
  • Packager: KATE SOMERVILLE SKINCARE LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 7, 2024

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  • ACTIVE INGREDIENTS

    ZINC OXIDE  17%

  • PURPOSE

    SUNSCREEN

  • USES

    • HELPS PREVENT SUNBURN.
    • IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS) DECREASES THE RISK OF SKIN 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:
    •      AT LEAST EVERY 2 HOURS
    •      IMMEDIATELY AFTER TOWEL DRYING
    • SUN PROTECTION MEASURES.
      SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING:

          LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 A.M.-2 P.M.

          WEAR LONG-SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES.

    • CHILDREN UNDER 6 MONTHS: ASK A DOCTOR.
  • INACTIVE INGREDIENTS

    AQUA/WATER/EAU, ISOAMYL LAURATE, POLYMETHYLSILSESQUIOXANE/SILICA CROSSPOLYMER, GLYCERIN, UNDECANE, ISODODECANE, BUTYLOCTYL SALICYLATE, CETEARYL DIMETHICONE, COCOGLYCERIDES, TRIDECANE, SODIUM CHLORIDE, LAURYL PEG-9, POLYDIMETHYLSILOXYETHYL DIMETHICONE, PROPANEDIOL, ETHYLHEXYL METHOXYCRYLENE, ECTOIN, TASMANNIA LANCEOLATA FRUIT/LEAF EXTRACT, HYDROXYECTOIN, CERAMIDE NP, TOCOPHERYL ACETATE, DISTEARDIMONIUM HECTORITE, COCONUT ALKANES, 1,2-HEXANEDIOL, PROPYLENE CARBONATE, SODIUM LAUROYL LACTYLATE, TRISODIUM ETHYLENEDIAMINE DISUCCINATE, CAPRYLHYDROXYAMIC ACID, COCO-CAPRYLATE/CAPRATE, CHOLESTEROL, XANTHAN GUM, CARBOMER, SODIUM CITRATE

  • OTHER INFORMATION

    • PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.
  • QUESTIONS?

    VISIT WWW.KATESOMERVILLE.COM OR CALL 1-800-984-5283.

  • PRINCIPAL DISPLAY PANEL

    01b UC_Daily Deflector Mineral Sunscreen_50mL

  • INGREDIENTS AND APPEARANCE
    DAILY DEFLECTOR MINERAL SUNSCREEN  SPF 40
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43479-209
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE10 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ISOBUTANE (UNII: BXR49TP611)  
    PROPANE (UNII: T75W9911L6)  
    ISODODECANE (UNII: A8289P68Y2)  
    ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    RHODIOLA ROSEA ROOT (UNII: 3S5ITS5ULN)  
    WATER (UNII: 059QF0KO0R)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    SILICA, TRIMETHYLSILYL CAPPED (UNII: VU10KU4B9S)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43479-209-521 in 1 BOX01/08/2021
    1NDC:43479-209-1250 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:43479-209-113 mL in 1 TUBE; Type 0: Not a Combination Product01/08/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/08/2021
    Labeler - KATE SOMERVILLE SKINCARE LLC (615155533)
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