Sunscreen Stick

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 Stick
Active ingredientOCTISALATE, ENSULIZOLE, HOMOSALATE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Homosalate 15%,0ctisalate 5%,Ensulizole 4%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Uses helps prevent sunbum 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 externall 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 ofreach ofchildren. 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 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. wearlong-sleeved shirts, pants, hats, and sunglasses
children under 6 months: Ask a doctor

INACTIVE INGREDIENT SECTION

C12‑15 Alkyl Benzoate
Caprylic/Capric Triglyceride
Isododecane
Neopentyl Glycol Diheptanoate
VP/Hexadecene Copolymer
Beeswax
Candelilla Wax
Microcrystalline Wax
Tocopherol (Vitamin E)
Caprylyl Glycol
Phenylpropanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label4label4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130644818950036GTIN-13: 0644818950036
EAN-13: 0644818950036
GTIN-12: 644818950036
UPC-A: 644818950036
GTIN storage (14 digits): 00644818950036
label4.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-015-01Sunscreen Stick75 g in 1 BOTTLESTICK751

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84938-01584938-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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 StickHOMOSALATE 15%, OCTISALLATE 5%, ENSULIZOLE 4%Foshan Sugar Max Cosmetics CO.,Ltd4637503c-46dc-68de-e063-6394a90abdc72025-12-18WarningsExact identifier
ndc (package): 84938-015-01
ndc (product): 84938-015
ndc11 (package): 84938001501
spl id: 4637503c-46dd-68de-e063-6394a90abdc7
spl set id: 4637503c-46dc-68de-e063-6394a90abdc7

Reported adverse events (FAERS/openFDA)#

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