FDA.reportPublic FDA data

DAILY DEFLECTOR MINERAL SUNSCREEN

Manufacturer
KATE SOMERVILLE SKINCARE LLC
Effective date
2025-01-12
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 20:42:58

Label at a glance#

ProductDAILY DEFLECTOR MINERAL SUNSCREEN SPF 40
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure10 sections

Indications and 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.

Dosage and administration

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...

Storage and handling

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE  17%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USES

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

STORAGE AND HANDLING SECTION

  • PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_Daily Deflector Mineral Sunscreen_50mL01b UC_Daily Deflector Mineral Sunscreen_50mL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43479-209DAILY DEFLECTOR MINERAL SUNSCREEN SPF 40 (ZINC OXIDE) LOTION [KATE SOMERVILLE SKINCARE LLC]7Legacy NDC20250113_e13cc127-c39c-4f3d-bd20-7484a5cb8530.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43479-20943479-209-12, 43479-209-52, 43479-209-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ISOBUTANEBXR49TP611IACT
PROPANET75W9911L6IACT
ISODODECANEA8289P68Y2IACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
POVIDONE, UNSPECIFIEDFZ989GH94EIACT
METHYL DIHYDROABIETATE7666FJ0J9FIACT
HYALURONIC ACIDS270N0TRQYIACT
RHODIOLA ROSEA ROOT3S5ITS5ULNIACT
WATER059QF0KO0RIACT
LAVENDER OILZBP1YXW0H8IACT
SILICA, TRIMETHYLSILYL CAPPEDVU10KU4B9SIACT
PENTYLENE GLYCOL50C1307PZGIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OXYBENZONE95OOS7VE0YACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
44ebf580-74c4-92ba-e063-6394a90a29dbe13cc127-c39c-4f3d-bd20-7484a5cb85302025-12-01WarningsExact identifier
spl set id: e13cc127-c39c-4f3d-bd20-7484a5cb8530

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.