ONSART MINERAL SUNSCREEN- zinc oxide 24% spray

ONSART Mineral Sunscreen by

Drug Labeling and Warnings

ONSART Mineral Sunscreen by is a Otc medication manufactured, distributed, or labeled by Guangzhou Huixue Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 24%

INACTIVE INGREDIENT

ALOE BARBADENSIS LEAF JUICE, DIBUTYL ADIPATE, ISOOCTANE, LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE, POLYHYDROXYSTEARIC ACID, DECYL GLUCOSIDE, PHENOXYETHANOL, TOCOPHEROL, BISABOLOL, SILICA, BUTYLENE GLYCOL, ETHYLHEXYLGLYCERIN, DIPOTASSIUM GLYCYRRHIZATE, STEARIC ACID, PROPYLENE GLYCOL, XANTHAN GUM, OPUNTIA DILLENII EXTRACT, OPHIOPOGON JAPONICUS ROOT EXTRACT, AVENA SATIVA BRAN EXTRACT, PAEONIA ALBIFLORA ROOT EXTRACT, SCUTELLARIA BAICALENSIS ROOT EXTRACT, GREEN TEA （CAMELLIA SINENSIS）EXTRACT, WATER, HYALURONIC ACID, CAPRYLYL GLYCOL, ISOBUTANE, TOCOPHERYL ACETATE.

PURPOSE

unscreen

INDICATIONS & USAGE

Uses Helps prevent sunburm. .l used as directed with other sun protection measures (see Directlens), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS

Warnings For enternal use only, - Danger. Flammable. Contents under pres - De not use near fire, heat or while smoking. Do not puncture or incinerate. Store at temperatures below 120*F (48C). - De not wse on damaged or braken skin. - When using this product, keep ouf of eyes. If contact occurs, rinse thoroughly with waler. . Stop use and aak a doctor if rash occurs. + Koop out of reach of chiidren. If swailowed, get medical help or contact a Poison Contrel Center iright away. - Usn only as directed. Intentional misuse by deliberately concentrating and inhaling the comtents can be harmful or fatal.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

WHEN USING

Directions - Shake well before sach use. Spray liberally and spread evenly by hand 15 minules before sun exppsure. Hald contsiner 4 tp & inches from the skin to apply.Rub in. -Do not apply in windy conditions. Use in a well-vent lated area. Reapply: Atter BD minutes of swimming. sweating .or immediately after towel drying A! leust every 2 hours. . Sun Protaction Measures: Spending time in the sun incresses your risk of skin cancer and early skin aging. To decrease this risk, reggularty use a sunscreen with a Biroed Spectrum SPF velue of 15 or higher and other sun protection measures includirg: - Limil time in the sun, especially from 10 am-2 pm. -Wsar long-slesve shiris, pands, hats, and Snglascs. Children under é months: Ask a doctor

STOP USE

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

DO NOT USE

You ae under 18 years of age, Do not use it on babies and children your scalp is red.inflamed.infected, irritated, or painful
You use other medicines on the scalp.Ask a doctor before use if you hace heart disease..

DOSAGE & ADMINISTRATION

Twice each day,4 sprays (1ml)each time. 50 days supply

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ONSART MINERAL SUNSCREEN 
zinc oxide 24% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87204-159
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	48 mg  in 200 g

Inactive Ingredients
Ingredient Name	Strength
CITRONELLOL (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
BENZYL BENZOATE (UNII: N863NB338G)
LINALYL ACETATE (UNII: 5K47SSQ51G)
MENTHOL (UNII: L7T10EIP3A)
AQUA (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HEXYL CINNAMAL (UNII: 7X6O37OK2I)
ALPHA-ISOMETHYL IONONE (UNII: 9XP4LC555B)
LINALOOL (UNII: D81QY6I88E)
GERANYL ACETATE (UNII: 3W81YG7P9R)
POGOSTEMON CABLIN OIL (UNII: F3IN55X5PO)
ACETYL CEDRENE (UNII: X6I62755AK)
AMYL SALICYLATE (UNII: VZO9C30208)
PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
COUMARIN (UNII: A4VZ22K1WT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87204-159-01	200 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/15/2026	01/26/2027

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/15/2026	01/26/2027

Labeler - Guangzhou Huixue Biotechnology Co., Ltd. (418186127)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Huixue Biotechnology Co., Ltd.		418186127	label(87204-159)