Ultra V IDEBENONE SKINFIT CUSHION

Manufacturer
Ultra V Co., Ltd | Kolmar Korea Co., Ltd.
Effective date
2018-01-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:03:54

Label at a glance#

ProductUltra V IDEBENONE SKINFIT CUSHION
Active ingredientTitanium Dioxide, Octinoxate, Zinc Oxide
Label structure7 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 10.06%, Ethylhexyl Methoxycinnamate 5.0%, Zinc Oxide 1.96%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Methylpropanediol, Cprylyl methicone, Coco-Caprylate/Caprate, Stearyl Dimethicone, Niacinamide, Trimethylsiloxysilicate, Diisostearyl malate, Magnesium Sulfate, Iron Oxides(CI 77492), Octadecene, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Sythetic Fluorphlogopite, Aminopropyl Dimethicone, Phenoxyethanol, Polymethylsilsesquioxane, Iron Oxides(CI 77491), Disteardimonium hectorite, Fragrance, Alumina, Ethylhexylglycerin, Silica, Iron, oxides(CI 77499), Octyldodecanol, Triethoxycaprylylsilane, Dextrin Palmitate, Xanthan Gum, Adenosine, Portulaca Oleracea Extract, Echium Plantagineum Seed Oil, Tocopheryl Acetate, Dimethicone, Butylene Glycol, Cardiospermum Halicacabum Flower/leaf/vine Extract, Hydroxydecul Ubiquinone, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Tocopherol, Bambusa Arundinacea Stem Extract, Moringa Oleifera Seed Oil, Maltodextrin, Ceramide NP, Persea Gratissima (Avocado) Oil, Copper Tripeptide-1, Saccharide Hydrolysate, Hydrolyzed Vegetable Protein, Alcohol, Caprylic/Capric Triglyceride, 1,2-Hexanediol, Phellinus Linteus Extract, Phellinus Linteus Extract, Hydrogenated Lecithin, Ganoderma Lucidum (Mushroom) Stem Extract, Punica Granatum Extract, Sodium Stearoyl Glutamate, Rosa Damascena Flower Oil, Cordyceps Sinensis Extract, Disodium EDTA, Sodium Ascorbyl Phosphate, Acetyl hexapeptide-8, sh-Oligopeptide-1

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: Helpe sunscreen agent skin

Directions: Coat proper amount of powder on powder-puff. Tap powder-puff on the face gently and complete make-up. If it is not blended in well or flaky or cakey make-up you may re-touch as mentioned above again in a couple of hours.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809533817626GTIN-13: 8809533817626
EAN-13: 8809533817626
GTIN storage (14 digits): 08809533817626
cushion carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71975-060-022023-06-08C16284748780-1f386c649-ef71-0266-e053-dadaa90a7c1a8c0f4ba9-2744-4712-81e2-8a20acbba16c
71975-060-022023-01-30C16284748780-1f386c649-ef71-0266-e053-dadaa90a7c1a8c0f4ba9-2744-4712-81e2-8a20acbba16c

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
71975-06071975-060-01, 71975-060-02

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
7ba26a28-595b-4d05-8e1a-6d8b3b6814648c0f4ba9-2744-4712-81e2-8a20acbba16c2023-06-08WarningsExact identifier
spl set id: 8c0f4ba9-2744-4712-81e2-8a20acbba16c

Reported adverse events (FAERS/openFDA)#

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