FDA.reportPublic FDA data

84938-006 SUNSCREEN SPRAY

Manufacturer
Foshan Sugar Max Cosmetics CO.,Ltd
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:25:53

Label at a glance#

ProductSUNSCREEN SPRAY150ml
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE, HOMOSALATE, OCTISALATE
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 sweating Immediately after towel drying "at least every 2 hours Sun Protection 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
Caprylic/Capric Triglyceride
Coco‑Caprylate/Caprate
Polyhydroxystearic Acid
Hydrogenated Poly(C6‑14 Olefin)
VP/Hexadecene Copolymer
Glycerin
Sodium PCA
Tocopherol
Caprylyl Glycol
Phenylpropanol
Polysorbate 20

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label2label2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130644818950128GTIN-13: 0644818950128
EAN-13: 0644818950128
GTIN-12: 644818950128
UPC-A: 644818950128
GTIN storage (14 digits): 00644818950128		label2.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-006-01SUNSCREEN SPRAY150ml150 mL in 1 BOTTLELIQUID1501

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84938-00684938-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
AQUA059QF0KO0RIACT
HYDROGENATED POLY(C6-14 OLEFIN; 2 CST)P0TX083987IACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
ZINC OXIDESOI2LOH54ZACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
VP/HEXADECENE COPOLYMERKFR5QEN0N9IACT
SODIUM PCA469OTG57A2IACT
TOCOPHEROLR0ZB2556P8IACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENYLPROPANOL0F897O3O4MIACT
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT

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 15%, TITANIUM DIOXIDE 6%, HOMOSALATE 5%, OCTISALATE 4%Foshan Sugar Max Cosmetics CO.,Ltd460ead6c-dd44-e320-e063-6294a90a2b642025-12-16WarningsExact identifier
ndc (package): 84938-006-01
ndc (product): 84938-006
ndc11 (package): 84938000601
spl id: 460ead6c-dd45-e320-e063-6294a90a2b64
spl set id: 460ead6c-dd44-e320-e063-6294a90a2b64

Reported adverse events (FAERS/openFDA)#

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