FDA.reportPublic FDA data

ALOHA MINERAL BLOCK-BRUSH ON MINERAL

Manufacturer
Aopline Biotechnology (Guangzhou) Co., Ltd.
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:32:02

Label at a glance#

ProductALOHA MINERAL BLOCK-BRUSH ON MINERAL
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium dioxide-19.5%

Zinc oxide-24%

OTC - PURPOSE SECTION

Sunscreen

WARNINGS SECTION

Flammable. Do not spray near heat sparks, sources of ignition, or flames.

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hour

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

When using this product: keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Mica, Vinyl Dimethicone/Methicone,Silsesquioxane Crosspolymer, Sodium Benzoate. Potassium Sorbate,Coconut Scent, Kaolin, Tocopherol,Rubus idaeus (Raspberry) Seed Oil, Daucus Carota Sativa (Carrot) Seed Oil,Oryza Sativa (Rice) Powder,Silica Dimethyl Silylate, Mango Scent,Magnesium Stearate, Stearic Acid,Camellia Sinensis Extract, Aloe Barbadensis Leaf Powder,Chrysanthellum Indicum Extract,Lophatherum Gracile Leaf Powder,Lavandula Angustifolia (Lavender) Oil,Ci 77492, Ci 77491, Ci 77499

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130198715200492GTIN-13: 0198715200492
EAN-13: 0198715200492
GTIN-12: 198715200492
UPC-A: 198715200492
GTIN storage (14 digits): 00198715200492		87283-004-01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87283-004-01ALOHA MINERAL BLOCK-BRUSH ON MINERAL6 g in 1 BOTTLEPOWDER61

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87283-00487283-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB
SILICA DIMETHYL SILYLATEEU2PSP0G0WIACT
MAGNESIUM STEARATE70097M6I30IACT
MICAV8A1AW0880IACT
RASPBERRY SEED OIL9S8867952AIACT
CHRYSANTHELLUM INDICUM TOPSTJ856D1Z0IACT
LAVENDER OILZBP1YXW0H8IACT
STEARIC ACID4ELV7Z65APIACT
COCONUT3RT3536DHYIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
RICE BRANR60QEP13ICIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
LOPHATHERUM GRACILE LEAFR417138GE9IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
TOCOPHEROLR0ZB2556P8IACT
CARROT SEED OIL595AO13F11IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
FERRIC OXIDE RED1K09F3G675IACT
KAOLIN24H4NWX5COIACT
ALOE VERA LEAFZY81Z83H0XIACT
MANGOI629I3NR86IACT
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
ALOHA MINERAL BLOCK-BRUSH ON MINERALSUNSCREEN SPF50Aopline Biotechnology (Guangzhou) Co., Ltd.47dd07aa-71b4-5d54-e063-6394a90a41272026-01-08WarningsExact identifier
ndc (package): 87283-004-01
ndc (product): 87283-004
ndc11 (package): 87283000401
spl id: 47dd07aa-71b5-5d54-e063-6394a90a4127
spl set id: 47dd07aa-71b4-5d54-e063-6394a90a4127

Reported adverse events (FAERS/openFDA)#

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