FDA.reportPublic FDA data

CALIFORNIA ALOE FRESH POW DERY SUN

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co.,Ltd. Bucheon Factory
Effective date
2026-01-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:32:43

Label at a glance#

ProductCALIFORNIA ALOE FRESH POW DERY SUN
Active ingredientHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure7 sections

Indications and uses

Protects skin from direct sunlight and UV rays.

Dosage and administration

Apply adequate amount of the product and thoroughly apply on the areas exposed to the UV rays. Apply the sunscreen product before exposure. Re-apply frequently to maintain protection, especially after perspiring, swimming or toweling.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

HOMOSALATE 9.0%
OCTOCRYLENE 9.0%
ETHYLHEXYL SALICYLATE 4.5%
BUTYL METHOXYDIBENZOYLMETHANE 2.9%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Protects skin from direct sunlight and UV rays.

WARNINGS

WARNINGS SECTION

For external use only. Avoid contact with eyes. In the event of contact with eyes, rinse thoroughly with water. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace cap after use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply adequate amount of the product and thoroughly apply on the areas exposed to the UV rays. Apply the sunscreen product before exposure. Re-apply frequently to maintain protection, especially after perspiring, swimming or toweling.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

POLYETHYLENE, PROPYLHEPTYL CAPRYLATE, DIMETHICONE, SILICA, ISOPROPYL PALMITATE, METHYL METHACRYLATE CROSSPOLYMER, POLYMETHYLSILSESQUIOXANE, DICAPRYLYL CARBONATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, ACRYLATES COPOLYMER, OZOKERITE, FRAGRANCE, LAURYL PEG-8 DIMETHICONE, DEHYDROACETIC ACID, POLYGLYCERYL-2 TRIISOSTEARATE, TOCOPHEROL, YELLOW 5 LAKE(CI 19140), WATER, SEA WATER, BUTYLENE GLYCOL, PHENOXYETHANOL, ALOE BARBADENSIS LEAF EXTRACT, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, MORINDA CITRIFOLIA EXTRACT, PENTYLENE GLYCOL, 1,2-HEXANEDIOL, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, LINALOOL, LIMONENE

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-532-012024-01-30C16284748780-11030e365-4e5c-111a-e063-dadaa90a10e2California Aloe Fresh Powdery Sun Stick SPF 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51346-532-01CALIFORNIA ALOE FRESH POW DERY SUN21 g in 1 CARTONSTICK215

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-53251346-532-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLHEPTYL CAPRYLATE991Z19V2ODIACT
DIMETHICONE92RU3N3Y1OIACT
HOMOSALATEV06SV4M95SACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB

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
CALIFORNIA ALOE FRESH POW DERY SUNHOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANENATURE REPUBLIC CO., LTD.aa10dbbf-97b3-4258-bbd3-0d8cc9935e122026-01-13WarningsExact identifier
ndc (package): 51346-532-01
ndc (product): 51346-532
ndc11 (package): 51346053201
spl id: 4840bbfd-c3c4-2904-e063-6394a90ac98b
spl set id: aa10dbbf-97b3-4258-bbd3-0d8cc9935e12

Reported adverse events (FAERS/openFDA)#

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