FDA.reportPublic FDA data

CALIFORNIA ALOE FRESH SUN MILK

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2014-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:36:35

Label at a glance#

ProductCALIFORNIA ALOE FRESH SUN MILK
Active ingredientZinc Oxide, Titanium Dioxide
Label structure8 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Zinc Oxide 12.48%, Titanium Dioxide 2.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Ingredients:
CYCLOPENTASILOXANE, WATER, ISODODECANE, BUTYLENE GLYCOL, DICAPRYLYL ETHER, GLYCERIN, METHYL METHACRYLATE CROSSPOLYMER, ALCOHOL, BIOSACCHARIDE GUM-1, CAPRYLYL METHICONE, NIACINAMIDE, CAPRYLIC/CAPRIC/SUCCINIC TRIGLYCERIDE, PEG-10 DIMETHICONE, POLYMETHYLSILSESQUIOXANE, PORTULACA OLERACEA EXTRACT, DIMETHICONE, MAGNESIUM SULFATE, METHICONE, ALOE BARBADENSIS LEAF EXTRACT, SILICA, PHENOXYETHANOL, FRAGRANCE, POLYGLYCERYL-6 POLYRICINOLEATE, ALUMINUM HYDROXIDE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, CAPRYLYL GLYCOL, STEARIC ACID, GLYCERYL CAPRYLATE, MORINDA CITRIFOLIA EXTRACT, SEA WATER, TOCOPHERYL ACETATE, ADENOSINE, POLYURETHANE-11, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT

PURPOSE

OTC - PURPOSE SECTION

Purpose: Brightening, Wrinkle-Improving, UV Protection

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

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

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use:
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
51346-244-012021-07-13C16284748780-19d75b9d0-22c0-f424-e053-dadaa90a57ce737c5568-0c72-4bc3-9f80-4900dda592e3
51346-244-012020-01-31C16284748780-19d75b9d0-22c0-f424-e053-dadaa90a57ce737c5568-0c72-4bc3-9f80-4900dda592e3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
Zinc OxideACTIVE INGREDIENTSOI2LOH54Z1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
51346-24451346-244-01

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
Zinc OxideSOI2LOH54ZACTIM
Titanium Dioxide15FIX9V2JPACTIB
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
92d2924d-5d32-4bca-9700-d1537f8b1872737c5568-0c72-4bc3-9f80-4900dda592e32021-07-13WarningsExact identifier
spl set id: 737c5568-0c72-4bc3-9f80-4900dda592e3

Reported adverse events (FAERS/openFDA)#

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