ONSART SUNSCREEN- zinc oxide 12% spray

ONSART SUNSCREEN by

Drug Labeling and Warnings

ONSART SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by Hainan Shengtaizhuo International Information Development Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ADVERSE REACTIONS

Zinc 0xide 12%,0ctisalate 5%, Avobenzone 3%,Octocrylene 3%.

PURPOSE

Helps prevent sunburn

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a poison control center right away.

WARNINGS

For external use only.Do not use on damaged or broken skin.When using this product keep out of eyes. Rinse with water to remove

INACTIVE INGREDIENT

WATER、CYCLOPENTASILOXANE、TITANIUM DIOXIDE、BUTYLENE GLYCOL、DICAPRYLYL CARBONATE、CETYL PEG/PPG-10/1 DIMETHICONE、SODIUM CHLORIDE、ETHYLHEXYL TRIAZONE、METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL、DISTEARDIMONIUM HECTORITE、PHENOXYETHANOL、SODIUM HYDROXIDE、ALUMINUM HYDROXIDE、STEARIC ACID、PROPYLENE CARBONATE、ACRYLATES/DIMETHICONE COPOLYMER、TOCOPHERYL ACETATE、DECYL GLUCOSIDE、TRIETHOXYCAPRYLYLSILANE、BISABOLOL、ETHYLHEXYLGLYCERIN、GLYCERIN、PROPYLENE GLYCOL、XANTHAN GUM、JASMINUM SAMBAC (JASMINE) LEAF CELL EXTRACT

DOSAGE & ADMINISTRATION

Helps prevent sunburn.if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by sun exposure.

INDICATIONS & USAGE

Helps prevent sunburn.if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by sun exposure.

PRINCIPAL DISPLAY PANEL

CRYSTAL SUNSCREEN SPRAY

INGREDIENTS AND APPEARANCE

ONSART SUNSCREEN 
zinc oxide 12% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84556-152
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.12 g  in 150 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.03 g  in 150 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.05 g  in 150 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.03 g  in 150 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
BISABOLOL (UNII: 24WE03BX2T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
ISOBUTANE (UNII: BXR49TP611)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
XANTHAN GUM (UNII: TTV12P4NEE)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
GLYCERIN (UNII: PDC6A3C0OX)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL (UNII: 8NT850T0YS)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Product Characteristics
Color		Score
Shape	ROUND	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84556-152-01	150 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/01/2025	09/17/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/01/2025	09/17/2026

Labeler - Hainan Shengtaizhuo International Information Development Co., LTD (976885514)

Establishment
Name	Address	ID/FEI	Business Operations
Hainan Shengtaizhuo International Information Development Co., LTD		976885514	manufacture(84556-152)