FDA.reportPublic FDA data

84938-013 Sunscreen Lotion

Manufacturer
Foshan Sugar Max Cosmetics CO.,Ltd
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:51:35

Label at a glance#

ProductSunscreen Lotion118mL
Active ingredientTITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE, HOMOSALATE
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 m reapply: after 80 minutes of swimming or sweating "lmmediately after towel drying "at least every 2 hours m Sun Protection Measures. Spending time in the sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and othersun 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)
Caprylic/Capric Triglyceride
C12‑15 Alkyl Benzoate
Coco‑Caprylate/Caprate
Polyhydroxystearic Acid
Glyceryl Stearate Citrate
Cetearyl Alcohol
Polyglyceryl‑6 Distearate
Glycerin
Sodium PCA
Tocopherol (Vitamin E)
Caprylyl Glycol
Phenylpropanol
Xanthan Gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label2label2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130644818950111GTIN-13: 0644818950111
EAN-13: 0644818950111
GTIN-12: 644818950111
UPC-A: 644818950111
GTIN storage (14 digits): 00644818950111		label2.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-013-01Sunscreen Lotion118mL118 mL in 1 BOTTLELOTION1183

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
84938-01384938-013-01

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
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
XANTHAN GUMTTV12P4NEEIACT
OCTISALATE4X49Y0596WACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
TOCOPHEROLR0ZB2556P8IACT
POLYGLYCERYL-6 DISTEARATEZ35I17EQOPIACT
ZINC OXIDESOI2LOH54ZACTIB
HOMOSALATEV06SV4M95SACTIB
CETEARYL ALCOHOL2DMT128M1SIACT
SODIUM PCA469OTG57A2IACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENYLPROPANOL0F897O3O4MIACT
GLYCERINPDC6A3C0OXIACT
AQUA059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-12-18full-release2026-06-01 01:26:22

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 Lotion118mLZINC OXIDE 15%, TITANIUM DIOXIDE 6%, HOMOSALATE 5%, OCTISALATE 4%Foshan Sugar Max Cosmetics CO.,Ltd46355437-4068-9d03-e063-6394a90ae52c2026-01-09WarningsExact identifier
ndc (package): 84938-013-01
ndc (product): 84938-013
ndc11 (package): 84938001301
spl id: 47effc7d-e100-49c4-e063-6394a90a3c5a
spl set id: 46355437-4068-9d03-e063-6394a90ae52c

Reported adverse events (FAERS/openFDA)#

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