FDA.reportPublic FDA data

84938-014 SUNSCREEN SPRAY

Manufacturer
Foshan Sugar Max Cosmetics CO.,Ltd
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:26:22

Label at a glance#

ProductSUNSCREEN SPRAY150mL
Active ingredientHOMOSALATE, ZINC OXIDE, TITANIUM DIOXIDE, OCTISALATE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 12%, Titanium Dioxide 6%, Homosalate14%, Octisalate 5%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Uses 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 the sun.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf product is swallowed, get medical help or contact a Poison Control Center right away. May stain some fabrics.

DOSAGE & ADMINISTRATION SECTION

Directions apply liberally 15 minutes before sun exposure reapply: after 80 minutes of swimming or sweating Immediately after towel drying "at least every 2 hours SunProtection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including: " limit time in the sun,especially from 10 a.m.-2 p.m.·wear long-sleeved shirts, pants hats, and sunglasses

children under 6 months: Ask a doctor

INACTIVE INGREDIENT SECTION

Aqua (Water)
C12‑15 Alkyl Benzoate
Isododecane
Neopentyl Glycol Diheptanoate
Phenylbenzimidazole Sulfonic Acid (Ensulizole)
VP/Hexadecene Copolymer
Polyglyceryl‑6 Stearate
Polyglyceryl‑6 Behenate
PEG‑40 Hydrogenated Castor Oil
Glycerin
Xanthan Gum
Tocopherol (Vitamin E)
Caprylyl Glycol
Phenylpropanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label3label3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130644818950029GTIN-13: 0644818950029
EAN-13: 0644818950029
GTIN-12: 644818950029
UPC-A: 644818950029
GTIN storage (14 digits): 00644818950029		label3.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-014-01SUNSCREEN SPRAY150mL150 mL in 1 BOTTLELIQUID1501

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84938-01484938-014-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
VP/HEXADECENE COPOLYMERKFR5QEN0N9IACT
POLYGLYCERYL-6 STEARATEETY9Q81E2TIACT
XANTHAN GUMTTV12P4NEEIACT
PHENYLBENZIMIDAZOLE SULFONIC ACID9YQ9DI1W42IACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
HOMOSALATEV06SV4M95SACTIB
AQUA059QF0KO0RIACT
PEG-40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
PHENYLPROPANOL0F897O3O4MIACT
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
ISODODECANEA8289P68Y2IACT
POLYGLYCERYL-6 BEHENATE4T2L7QI313IACT
CAPRYLYL GLYCOL00YIU5438UIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
OCTISALATE4X49Y0596WACTIB
GLYCERINPDC6A3C0OXIACT
TOCOPHEROLR0ZB2556P8IACT

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
SUNSCREEN SPRAY150mLZINC OXIDE 12%, TITANIUM DIOXIDE 6%, HOMOSALATE 14%, OCTISALATE 5%Foshan Sugar Max Cosmetics CO.,Ltd4635f90a-bbc9-0676-e063-6394a90a9f352025-12-18WarningsExact identifier
ndc (package): 84938-014-01
ndc (product): 84938-014
ndc11 (package): 84938001401
spl id: 4635f90a-bbca-0676-e063-6394a90a9f35
spl set id: 4635f90a-bbc9-0676-e063-6394a90a9f35

Reported adverse events (FAERS/openFDA)#

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