SUPREME SKINPIA 10 BB

Manufacturer
EBAIN Corporation Co., Ltd.
Effective date
2014-03-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:38:36

Label at a glance#

ProductSUPREME SKINPIA 10 BB
Active ingredientTitanium Dioxide, Zinc Oxide
Label structure8 sections

Indications and uses

Indications and usage: After basic skin care, apply adequate amount following the skin texture and gently tap to enhance absorption.

Dosage and administration

Dosage and administration: Take an adequate amount of this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Titanium Dioxide 10%, Zinc Oxide 0.6%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Cyclopentasiloxane, Phenyl Trimethicone, Caprylic/Capric Triglyceride, Cyclohexasiloxane, Butylene Glycol Dicaprylate/Dicaprate, Dicaprylyl Carbonate, Glycerin, Cetyl PEG/PPG-10/1 Dimethicone, Niacinamide, Sodium Chloride, Stearic Acid, Pentylene Glycol,
Sorbitan Isostearate, Aluminum Hydroxide, Methyl Methacrylate Crosspolymer, Beeswax, Persicaria Hydropiper Extract, 1,2-Hexanediol, Butylene Glycol, Phenoxyethanol, CI 77492, Stearalkonium Hectorite, Dimethicone Crosspolymer, Dimethiconol, Fragrance, Caprylhydroxamic Acid, CI 77491, Portulaca Oleracea Extract, Ultramarines, Coptis Japonica Root Extract, Corydalis Turtschaninovii Root Extract, Quercus Mongolia Leaf Extract, Larix Sibirica Wood Extract, Asarum Sieboldi Root Extract, Rheum Palmatum Root/Stalk Extract, Chrysanthellum Indicum Extract, Illicium Verum (Anise) Fruit Extract, Machilus Thunbergii Bark Extract, CI 77499, Disodium EDTA, Fomes Officinalis (Mushroom) Extract, Triethoxycaprylylsilane, Talc, Hydrogen Dimethicone, Ethylhexylglycerin, Lepidium Meyenii Root Extract,
Sarcodon Aspratus Extract, Sodium Hyaluronate, PEG-40 Hydrogenated Castor Oil, Polyglutamic Acid

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:
1. In case of having following symptoms after using this, you're advised to stop using it immediately.
If you keep using it, the symptoms will get worse and need to consult a dermatologist.
- In case of haviong problems such as red rash, swollenness, itching, stimulation during usage.
- In case of having the same symptoms above on the part you put this product on by direct sunlight.
2. You are banned to use it on the part where you have a scar, eczema, or dermatitis.
3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: Keep out of reach of babies and children

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Indications and usage: After basic skin care, apply adequate amount following the skin texture and gently tap to enhance absorption.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62242-020-012019-11-27C16284748780-19855e2a2-4164-60a7-e053-dbdaa90a05bdf7099b63-5df3-49f3-ba86-22ee4243342c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62242-020-01SUPREME SKINPIA 10 BB50 mL in 1 CARTONCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62242-020SUPREME SKINPIA 10 BB (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [EBAIN CORPORATION CO., LTD.]1Legacy NDC, 1 package rows20140304_f7099b63-5df3-49f3-ba86-22ee4243342c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
Zinc OxideACTIVE INGREDIENTSOI2LOH54Z1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
Phenyl TrimethiconeINACTIVE INGREDIENTDR0K5NOJ4R1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62242-02062242-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
9dcf88b4-206c-4157-9674-9ee58e639748f7099b63-5df3-49f3-ba86-22ee4243342c2014-03-04WarningsExact identifier
spl id: 9dcf88b4-206c-4157-9674-9ee58e639748
spl set id: f7099b63-5df3-49f3-ba86-22ee4243342c

Reported adverse events (FAERS/openFDA)#

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