POLYSILICONE-15 - HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED

Manufacturer
HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED
Effective date
2026-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-05 00:30:39

Label at a glance#

ProductANESSA PERFECT UV SUNSCREEN SKINCARE
Active ingredientHOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS PURPOSE

Ethylhexyl Salicylate4%................................................................ Sunscreen

Homosalate 8%................................................................................. Sunscreen

Octocrylene8%............................................. Sunscreen

OTC - PURPOSE SECTION

Sunscreen

Uses:

Helps prevent sunburn, decreases the risk of skin cancer and early skin aging if used as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

When using this product, keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. In case of ingestion, get medical help or

contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply evenly to clean, dry skin before sun exposure. Apply once-daily.

INACTIVE INGREDIENT SECTION

Water, Dimethicone, Diisopropyl Sebacate, Homosalate, Isohexadecane, Silica, Alcohol, Octocrylene, Ethylhexyl Salicylate, Dipropylene Glycol, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Polysilicone-15, Diethylamino Hydroxybenzoyl Hexyl Benzoate, C12-15 Alkyl Benzoate, Ethylhexyl Triazone, Dextrin Palmitate, Sorbitan Sesquiisostearate, Glycerin, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Trimethylsiloxysilicate, Disteardimonium Hectorite, Isostearic Acid, PEG-9 Polydimethylsiloxyethyl Dimethicone Other Trace Ingredients: Sodium Citrate, Tocopherol (Vitamin E), EDTA Trisodium, BHT, Fragrance (Parfum), Butylene Glycol, Synthetic Fluorphlogopite, Stearic Acid, PEG/PPG-14/7 Dimethyl Ether, PEG/PPG-9/2 Dimethyl Ether, Dipotassium Glycyrrhizate, PEG-6, Camellia Sinensis Leaf Extract, Potentilla Erecta Root Extract, Acetylated Sodium Hyaluronate, Soluble Collagen, Phenoxyethanol

INDICATIONS & USAGE SECTION

event of prolonged sun exposure, apply standard sunscreen as-needed

throughout day

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130729238212244GTIN-13: 0729238212244
EAN-13: 0729238212244
GTIN-12: 729238212244
UPC-A: 729238212244
GTIN storage (14 digits): 00729238212244
87719-001-01.jpg
Data codeData Matrix22646864000287719-001-01.jpg

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87719-00187719-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 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
ANESSA PERFECT UV SUNSCREEN SKINCAREHOMOSALATE OCTOCRYLENE ETHYLHEXYL SALICYLATEHONGKONG JIAHE INTERNATIONAL HOLDING LIMITED5347c9a1-2239-b617-e063-6294a90ac6012026-06-02WarningsExact identifier
ndc (package): 87719-001-01
ndc (product): 87719-001
ndc11 (package): 87719000101
spl id: 5347c9a1-223a-b617-e063-6294a90ac601
spl set id: 5347c9a1-2239-b617-e063-6294a90ac601

Reported adverse events (FAERS/openFDA)#

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