FDA.reportPublic FDA data

TAKO PORE SEBUM SUN

Manufacturer
TONY MOLY CO.,LTD
Effective date
2018-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:09

Label at a glance#

ProductTAKO PORE SEBUM SUN
Active ingredientOctocrylene, Homosalate, Octisalate, Avobenzone, Octinoxate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Octocrylene 5.00%, Homosalate 5.00%, Ethylhexyl Salicylate 4.50%, Butyl Methoxydibenzoylmethane 4.00%, Ethylhexyl Methoxycinnamate 3.50%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Dimethicone, Polyethylene, Ethylhexyl Palmitate, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Diphenylsiloxy Phenyl Trimethicone, Microcrystalline Wax, Polysilicone-15, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Fragrance, Tocopheryl Acetate, Caprylyl Glycol, Eclipta Prostrata Extract, Melia Azadirachta Leaf Extract, Moringa Oleifera Seed Oil, Water, Panthenol, Calamine, Nelumbo Nucifera Flower Water, Sea Water, Centella Asiatica Extract, 1,2-Hexanediol, Algae Extract, Chlorella Vulgaris Extract, Hizikia Fusiforme Extract, Hydrolyzed Collagen

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

For external use only

Avoid contact with eyes.

Discontinue use if signs of irritation or rashes appear.

Replace the cap after use.

Keep Out of Reach of Children

DESCRIPTION

DESCRIPTION SECTION

Uses:

- helps prevent sunburn

- If used as directed with other sun protection measures

Directions:

Take an appropriate amount, evenly apply to face and body anywhere to be exposed to UV rays. Use as the last step of basic skin care.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59078-326-022020-01-31C16284748780-19d75b9d0-50b9-f424-e053-dadaa90a57ce00bf17c2-d1fb-4f1f-b30b-519aa80fef5c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59078-326-01TAKO PORE SEBUM SUN9.5 g in 1 CONTAINERSTICK9.51
59078-326-02TAKO PORE SEBUM SUN1 in 1 CARTONSTICK11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59078-326TAKO PORE SEBUM SUN (OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE, OCTINOXATE) STICK [TONY MOLY CO.,LTD]1Legacy NDC, 2 package rows20180404_00bf17c2-d1fb-4f1f-b30b-519aa80fef5c.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59078-32659078-326-01, 59078-326-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
Octocrylene5A68WGF6WMACTIB
HomosalateV06SV4M95SACTIB
Octisalate4X49Y0596WACTIB
AvobenzoneG63QQF2NOXACTIB
Octinoxate4Y5P7MUD51ACTIB
Dimethicone92RU3N3Y1OIACT
Ethylhexyl Palmitate2865993309IACT

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
6c95982c-c922-4815-95c0-897605186cc200bf17c2-d1fb-4f1f-b30b-519aa80fef5c2018-04-04WarningsExact identifier
spl id: 6c95982c-c922-4815-95c0-897605186cc2
spl set id: 00bf17c2-d1fb-4f1f-b30b-519aa80fef5c

Reported adverse events (FAERS/openFDA)#

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