FDA.reportPublic FDA data

ONSART SUNSCREEN

Manufacturer
Hainan Shengtaizhuo International Information Development Co., LTD
Effective date
2025-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:36:01

Label at a glance#

ProductONSART SUNSCREEN
Active ingredientZINC OXIDE, AVOBENZONE, OCTISALATE, OCTOCRYLENE
Label structure8 sections

Label contents#

Full prescribing information#

ADVERSE REACTIONS SECTION

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

OTC - PURPOSE SECTION

Helps prevent sunburn

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

WARNINGS SECTION

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 SECTION

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 SECTION

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 SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CRYSTAL SUNSCREEN SPRAY CRYSTAL SUNSCREEN SPRAYCRYSTAL SUNSCREEN SPRAY

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
84556-15284556-152-01

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
ZINC OXIDESOI2LOH54ZACTIB
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
STEARIC ACID4ELV7Z65APIACT
BISABOLOL24WE03BX2TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
OCTISALATE4X49Y0596WACTIB
DICAPRYLYL CARBONATE609A3V1SUAIACT
PROPYLENE CARBONATE8D08K3S51EIACT
ISOBUTANEBXR49TP611IACT
SODIUM HYDROXIDE55X04QC32IIACT
XANTHAN GUMTTV12P4NEEIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
SODIUM CHLORIDE451W47IQ8XIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
GLYCERINPDC6A3C0OXIACT
OCTOCRYLENE5A68WGF6WMACTIB
DECYL GLUCOSIDEZ17H97EA6YIACT
ETHYLHEXYL TRIAZONEXQN8R9SAK4IACT
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL8NT850T0YSIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
3fd26aba-ebaf-6f71-e063-6294a90ade0b397b272f-4ea4-3d6b-e063-6394a90aab2c2025-09-27Warnings, Adverse reactionsExact identifier
spl set id: 397b272f-4ea4-3d6b-e063-6394a90aab2c

Reported adverse events (FAERS/openFDA)#

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