SKYLAKE SUNSCREEN

Manufacturer
SKYLAKE | SkyLake Co., Ltd.
Effective date
2019-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:51

Label at a glance#

ProductSKYLAKE SUNSCREEN
Active ingredientOctinoxate, Zinc Oxide, Titanium Dioxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethylhexyl Methoxycinnamate 7.5%, Zinc Oxide 7%, Titanium Dioxide 5.41%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Water, Cyclomethicone, Butylene Glycol, Caprylic/Capric Triglyceride, Dimethicone Copolyol, CetylPEG/PPG-10/1Dimethicone, Glycerin, Arbutin, Scutellaria Baicalensis Root Extract, Paeonia Suffruticosa Root Extract, Morus Bombycis Leaf Extract, Angelica Gigas Extract, Mentha Piperita(Peppermint) Leaf Extract, Morus Alba Bark Extract, Cnidium Officinale Root Extract, Glycyrrhiza Glabra(Licorice) Root Extract, Hamamelis Virginiana(Witch Hazel) Bark/Leaf Extract, Rosa Centifolia Flower Extract, Cosmos Sulphureus Flower/Leaf/Stem Extract, Jasminum Officinale(Jasmine) Flower Extract, Lilium Candidum Flower Extract, Iris Ensata Extract, Hibiscus Rosa-Sinensis Flower/Leaf Extract , Nelumbo Nucifera Flower Extract, Cetyl Ethylhexanoate, Artemisia Absinthium Extract, Angelica Dahurica Root Extract, Pueraria Lobata Root Extract,Polyethylene, C20-40Acid, Beeswax, Phenyl Trimethicone, Inula Helenium Extract, Laminaria Japonica Extract, Sodium Chloride, Phellodendron Amurense Bark Extract, Eugenia Caryophyllus(Clove) Flower Extract, Disodium EDTA, Adenosine, Dimethicone, Talc, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:


Discontinue use if skin irritation develops. Use only as directed. Store in a cool dark place, avoid high temperatures and exposure to strong sunlight.

DESCRIPTION

DESCRIPTION SECTION

Uses:
This natural Sunscreen utilizes only natural preservative and herbal extract such as seven flowers and witch hazel. It shields your skin against harmful UVA/UVB effectively without irritating and drying your skin.

Directions:
Apply liberally on cleansed skin daily, especially on the body parts exposed to the sun. Re-apply after perspiring, swimming or every 4 hours under the sun.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809124633055GTIN-13: 8809124633055
EAN-13: 8809124633055
GTIN storage (14 digits): 08809124633055
sun carton.jpg

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53798-02053798-020-01, 53798-020-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a3e2acce-71d0-4d59-8dcf-a61a4a4062c11d1fbc7e-e4a7-449e-99ec-af209fc9bcf42021-05-31WarningsExact identifier
spl set id: 1d1fbc7e-e4a7-449e-99ec-af209fc9bcf4

Reported adverse events (FAERS/openFDA)#

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