FDA.reportPublic FDA data

CALIFORNIA ALOE MOISTURIZING TONE UP SUN BLOCK

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong Factory
Effective date
2022-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:04:34

Label at a glance#

ProductCALIFORNIA ALOE MOISTURIZING TONE UP SUN BLOCK
Active ingredientTITANIUM DIOXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

TITANIUM DIOXIDE 2.3%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, DIBUTYL ADIPATE, PROPANEDIOL, ETHYLHEXYL TRIAZONE, TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID, ALCOHOL, GLYCERIN, COCO-CAPRYLATE/CAPRATE, NIACINAMIDE, TROMETHAMINE, POLYGLYCERYL-3 DISTEARATE, 1,2-HEXANEDIOL, PENTYLENE GLYCOL, CAPRYLYL METHICONE, CETEARYL ALCOHOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, POLYSILICONE-15, CAPRYLIC/CAPRIC/SUCCINIC TRIGLYCERIDE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, GLYCERYL STEARATE, POLYMETHYLSILSESQUIOXANE, POTASSIUM CETYL PHOSPHATE, METHYLPROPANEDIOL, POLYHYDROXYSTEARIC ACID, CARBOMER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALUMINA, TRIETHOXYCAPRYLYLSILANE, GLYCERYL STEARATE CITRATE, ETHYLHEXYLGLYCERIN, ARTEMISIA VULGARIS OIL, ADENOSINE, SEA WATER, POLYETHER-1, BUTYLENE GLYCOL, PVM/MA COPOLYMER, SODIUM POLYACRYLATE, PHENOXYETHANOL, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, MORINDA CITRIFOLIA EXTRACT, BIOSACCHARIDE GUM-1, TOCOPHEROL

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

WARNINGS

WARNINGS SECTION

For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children.

DESCRIPTION

DESCRIPTION SECTION

Uses
Helps prevent sunburn while moisturizing and providing tone-up effect

Directions
Apply an appropriate amount to the skin before exposure.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-54051346-540-01, 51346-540-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
WATER059QF0KO0RIACT
DIBUTYL ADIPATEF4K100DXP3IACT
PROPANEDIOL5965N8W85TIACT

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
aa1c7f17-b878-4bdf-80ea-6d730129b71229203ca0-42df-4667-9a64-e69131c385d32022-06-28WarningsExact identifier
spl set id: 29203ca0-42df-4667-9a64-e69131c385d3

Reported adverse events (FAERS/openFDA)#

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