ALOHA MINERAL BLOCK-BRUSH ON MINERAL- sunscreen spf50 powder

ALOHA MINERAL BLOCK-BRUSH ON MINERAL by

Drug Labeling and Warnings

ALOHA MINERAL BLOCK-BRUSH ON MINERAL by is a Otc medication manufactured, distributed, or labeled by Aopline Biotechnology (Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Titanium dioxide-19.5%

Zinc oxide-24%

PURPOSE

Sunscreen

WARNINGS

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

DOSAGE & ADMINISTRATION

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

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALOHA MINERAL BLOCK-BRUSH ON MINERAL 
sunscreen spf50 powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87283-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	19.5 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	24 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICA (UNII: V8A1AW0880)
RASPBERRY SEED OIL (UNII: 9S8867952A)
CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0)
LAVENDER OIL (UNII: ZBP1YXW0H8)
STEARIC ACID (UNII: 4ELV7Z65AP)
COCONUT (UNII: 3RT3536DHY)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
RICE BRAN (UNII: R60QEP13IC)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
LOPHATHERUM GRACILE LEAF (UNII: R417138GE9)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
TOCOPHEROL (UNII: R0ZB2556P8)
CARROT SEED OIL (UNII: 595AO13F11)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
FERRIC OXIDE RED (UNII: 1K09F3G675)
KAOLIN (UNII: 24H4NWX5CO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANGO (UNII: I629I3NR86)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87283-004-01	6 g in 1 BOTTLE; Type 0: Not a Combination Product	01/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/08/2026

Labeler - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)