FDA.reportPublic FDA data

CALIFORNIA ALOE DAILY SUN BLOCK

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc.
Effective date
2019-01-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:33:25

Label at a glance#

ProductCALIFORNIA ALOE DAILY SUN BLOCK
Active ingredientHomosalate, Octisalate, Titanium Dioxide, Avobenzone
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Homosalate 10.0%, Ethylhexyl Salicylate 5.0%, Titanium Dioxide 4.32%, Butyl Methoxydibenzoylmethane 3.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
WATER, GLYCERIN, BUTYLENE GLYCOL, ETHYLHEXYL PALMITATE, CYCLOPENTASILOXANE, ACRYLATES COPOLYMER, NEOPENTYL GLYCOL DIHEPTANOATE, NIACINAMIDE, PROPANEDIOL, CYCLOHEXASILOXANE, POLYMETHYLSILSESQUIOXANE, CAPRYLYL METHICONE, DIMENTHICONE, CETEARYL ALCOHOL, TRICETEARETH-4 PHOSPHATE, GLYCERYL STEARATE, PEG-100 STEARATE, GLYCOL STEARATE, SILICA, PEG-2 STEARATE, POTASSIUM CETYL PHOSPHATE, SORBITAN SESQUIOLEATE, PHENOXYETHANOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, FRAGANCE(PARFUM), TROMETHAMINE, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, SEA WATER, ADENOSINE, XANTHAN GUM, IRON OXIDES(CI 774692), DISODIUM EDTA, IRON OXIDES(CI 77491), HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, TRIETHOXYCAPRYLYSILANE, MORINDA CITRIFOLIA FRUIT EXTRACT, LEUCONOSTOC/RADISH ROOTH FERMENT FILTRATE, ALOE BARBADENSIS LEAF EXTRACT, PENTYLENE GLYCOL, SODIUM BENZOATE, CITRIC ACID, 1,2-HEXANEDIOL, POLYQUATERNIUM-51

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.
A moisture-rich daily sun block that purifies and corrects your skin tone.

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-488-022021-06-23C16284748780-1ba0f9c33-0f25-a910-e053-dadaa90a0b85e7471163-175c-4dc3-9f37-79bd93879926
51346-488-022021-01-29C16284748780-1ba0f9c33-0f25-a910-e053-dadaa90a0b85e7471163-175c-4dc3-9f37-79bd93879926

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
51346-48851346-488-01, 51346-488-02

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
HomosalateV06SV4M95SACTIB
Octisalate4X49Y0596WACTIB
Titanium Dioxide15FIX9V2JPACTIB
AvobenzoneG63QQF2NOXACTIB
WATER059QF0KO0RIACT

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
4d51f382-8947-4918-ac0f-f6bdac4e5779e7471163-175c-4dc3-9f37-79bd938799262021-06-23WarningsExact identifier
spl set id: e7471163-175c-4dc3-9f37-79bd93879926

Reported adverse events (FAERS/openFDA)#

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