FDA.reportPublic FDA data

Sunscreen Cream

Manufacturer
Foshan Sugar Max Cosmetics CO.,Ltd
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:25:55

Label at a glance#

ProductSunscreen Cream
Active ingredientHOMOSALATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 15%, Titanium Dioxide 6%, Homosalate 5%, Octisalate 4%

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 sweatingImmediately after towel drying "at least every 2 hours SunProtection Measures. Spending time in the sun increases yourrisk 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 children under 6 months:shirts, pants, hats, and sunglassesAsk a doctor.

INACTIVE INGREDIENT SECTION

Aqua (Water)
Caprylic/Capric Triglyceride
Dimethicone
Glycerin
Sodium Hyaluronate (Hydrolyzed)
Glyceryl Stearate
Cetearyl Alcohol
Ammonium Acryloyldimethyltaurate/VP Copolymer
Phenoxyethanol
Ethylhexyl Glycerin
Hydroxyacetophenone
Aluminum Hydroxide
Stearic Acid
Triethoxycaprylylsilane

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130644818950104GTIN-13: 0644818950104
EAN-13: 0644818950104
GTIN-12: 644818950104
UPC-A: 644818950104
GTIN storage (14 digits): 00644818950104		label1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-012-01Sunscreen Cream90 mL in 1 BOTTLECREAM901

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
84938-01284938-012-01

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
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
HOMOSALATEV06SV4M95SACTIB
SODIUM HYALURONATEYSE9PPT4THIACT
CETEARYL ALCOHOL2DMT128M1SIACT
AQUA059QF0KO0RIACT
OCTISALATE4X49Y0596WACTIB
STEARIC ACID4ELV7Z65APIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERINPDC6A3C0OXIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
ZINC OXIDESOI2LOH54ZACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
GLYCERYL STEARATE230OU9XXE4IACT

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 CreamZINC OXIDE 15%,TITANIUM DIOXIDE 6%,HOMOSALATE 5%,OCTISALATE 4%Foshan Sugar Max Cosmetics CO.,Ltd46224dbe-a0fb-c242-e063-6394a90a26342025-12-17WarningsExact identifier
ndc (package): 84938-012-01
ndc (product): 84938-012
ndc11 (package): 84938001201
spl id: 46224dbe-a0fc-c242-e063-6394a90a2634
spl set id: 46224dbe-a0fb-c242-e063-6394a90a2634

Reported adverse events (FAERS/openFDA)#

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