FDA.reportPublic FDA data

CALIFORNIA ALOE AQUA SUN

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co., Ltd.
Effective date
2019-01-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:33:25

Label at a glance#

ProductCALIFORNIA ALOE AQUA SUN
Active ingredientOCTOCRYLENE, OCTINOXATE, OCTISALATE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: OCTOCRYLENE 9.00%, ETHYLHEXYL METHOXYCINNAMATE 7.00%, ETHYLHEXYL SALICYLATE 4.50%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
OCTYLDODECANOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, DICAPRYLYL CARBONATE, DIBUTYL LAUROYL GLUTAMIDE, SILICA SILYLATE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, TOCOPHERYL ACETATE, DIBUTYL ETHYLHEXANOYL GLUTAMIDE, ECHIUM PLANTAGINEUM SEED OIL, CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES, ALOE BARBADENSIS LEAF EXTRACT, MORINDA CITRIFOLIA EXTRACT, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, BISABOLOL, HYDROXYACETOPHENONE, SEA WATER, WATER, BUTYLENE GLYCOL, FRAGRANCE, PHENOXYETHANOL

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:
For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace the cap after use.

DESCRIPTION

DESCRIPTION SECTION

Uses:
Brightening, Wrinkle-Improvement, UV Protection.
The matte sun stick protects the skin from strong UV rays as it softly applies on the skin.

Directions: 

Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays..

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 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-51651346-516-01, 51346-516-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTOCRYLENE5A68WGF6WMACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OCTYLDODECANOL461N1O614YIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT

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
00683266-bb21-44ea-ba4a-34ea4a8588b2e157eaf9-581a-4ed3-bac9-2736c71ca2992021-07-13WarningsExact identifier
spl set id: e157eaf9-581a-4ed3-bac9-2736c71ca299

Reported adverse events (FAERS/openFDA)#

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