KATE SOMERVILLE (as PLD) - DAILY DEFLECTOR MINERAL SUNSCREEN SPF 40 (43479-209)

DAILY DEFLECTOR MINERAL SUNSCREEN by

Drug Labeling and Warnings

DAILY DEFLECTOR MINERAL SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by KATE SOMERVILLE SKINCARE LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DAILY DEFLECTOR MINERAL SUNSCREEN SPF 40- zinc oxide lotion 
KATE SOMERVILLE SKINCARE LLC

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KATE SOMERVILLE (as PLD) - DAILY DEFLECTOR MINERAL SUNSCREEN SPF 40 (43479-209)

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. 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.

01b UC_Daily Deflector Mineral Sunscreen_50mL

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 BOX01/08/202112/01/2025
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 Product01/08/202112/01/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/08/202112/01/2025
Labeler - KATE SOMERVILLE SKINCARE LLC (615155533)

Revised: 12/2025