Ultra V IDEBENONE SUNBLOCK

Manufacturer
Ultra V Co., Ltd | Kolmar Korea Co., Ltd.
Effective date
2018-12-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:39:24

Label at a glance#

ProductUltra V IDEBENONE SUNBLOCK
Active ingredientHomosalate, AVOBENZONE, ENSULIZOLE
Label structure7 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Homosalate 10%, Butyl Methoxydibenzoylmethane 3.5%, Phenylbenzimidazole Sulfonic Acid 3.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Glycerin, Acrylates Copolymer, Dibutyl Adipate, Methyl Methacrylate Crosspolymer, Niacinamide, Propanediol, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Pentylene Glycol, Alcohol Denat., Aminomethyl Propanol, Caprylyl Methicone, Polymethylsilsesquioxane, Dimethicone, Behenyl Alcohol, Glyceryl Stearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Carbomer, Phenoxyethandl, Tromethamine, Caprylyl Glycol, Xanthan Gum, Adenosine, Disodium EDTA, Boswellia Carterii Oil, Pelargonium Graveolens Flower Oil, Vetiveria Zizanoides Root Oil, Amyris Balsamifera Bark Oil, Butylene Glycol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Daucus Carota Sativa (Carrot) Seed Oil, Hydrocydecyl Ubiquinone, Tocopheryl Acetate, Macadamia Integrifolia Seed Oil, Anthemis Nobilis Flower Water, Octyldodecanol, Curcuma Longa (Turmeric) Root Extract, Rice Ferment Filtrate (Sake), Dipropylene Glycol, Aspalathus Linearis Leaf Extract, Lactobacillus/Rice Ferment Filtrate, Saccharomyces/Camellia Sinensis Extract Ferment Filtrate, Propylene Glycol, Sodium Palmitoyl Proline, Rose Flower Oil, Averrhoa Carambola Fruit Extract, Lactobacillus Ferment, Echium Plantagineum Seed Oil, Nymphaea Alba Flower Extract, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, 1,2-Hexanediol, Lactobacillus Ferment Filtrate, Lepidium Meyenii Root Extract, Mannitol, Vanilla Tahitensis Fruit Extract, Royal Jelly Extract, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Magnolia Biondii Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Sodium Benzoate, Ethylhexylglycerin, Benzyl Alcohol, Chrysanthemum Boreale Flower Extract, Citric Acid, Potassium Sorbate, Tocopherol, Limonia Acidissima Extract, , Acetyl Hexapeptide-8, Dehydroacetic Acid, Hydrolyzed Coral, sh-Decapeptide-7, sh-Octapeptide-4, sh-Oligopeptide-9, sh-Pentapeptide-19, 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: Apply liberally and uniformly to all exposed areas before sun exposure. Reapply often(every 2hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809551731133GTIN-13: 8809551731133
EAN-13: 8809551731133
GTIN storage (14 digits): 08809551731133
sunblock carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71975-070-022023-06-08C16284748780-1f386c649-fbec-0266-e053-dadaa90a7c1a98f96fbc-7607-4057-83f1-562fce9f6ea5
71975-070-022023-01-30C16284748780-1f386c649-fbec-0266-e053-dadaa90a7c1a98f96fbc-7607-4057-83f1-562fce9f6ea5

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
71975-07071975-070-01, 71975-070-02

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
5d8258b3-a9a4-4c19-bd71-d0bca58027d898f96fbc-7607-4057-83f1-562fce9f6ea52023-06-08WarningsExact identifier
spl set id: 98f96fbc-7607-4057-83f1-562fce9f6ea5

Reported adverse events (FAERS/openFDA)#

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