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#
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
Active ingredients: Homosalate 10%, Butyl Methoxydibenzoylmethane 3.5%, Phenylbenzimidazole Sulfonic Acid 3.5%
INACTIVE INGREDIENT
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
Purpose: Sunscreen
WARNINGS
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
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
QUESTIONS
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 8809551731133 | GTIN-13: 8809551731133 EAN-13: 8809551731133 GTIN storage (14 digits): 08809551731133 | sunblock carton.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71975-070-02 | 2023-06-08 | C162847 | 48780-1 | f386c649-fbec-0266-e053-dadaa90a7c1a | 98f96fbc-7607-4057-83f1-562fce9f6ea5 |
| 71975-070-02 | 2023-01-30 | C162847 | 48780-1 | f386c649-fbec-0266-e053-dadaa90a7c1a | 98f96fbc-7607-4057-83f1-562fce9f6ea5 |
Products#
Every source-derived product name is available through these pages.
- Ultra V IDEBENONE SUNBLOCK
- Homosalate, AVOBENZONE, ENSULIZOLE
- Homosalate
- AVOBENZONE
- ENSULIZOLE
- Water
- Glycerin
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71975-070 | 71975-070-01, 71975-070-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Homosalate | V06SV4M95S | ACTIB |
| AVOBENZONE | G63QQF2NOX | ACTIB |
| ENSULIZOLE | 9YQ9DI1W42 | ACTIB |
| Water | 059QF0KO0R | IACT |
| Glycerin | PDC6A3C0OX | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5d8258b3-a9a4-4c19-bd71-d0bca58027d8 | 98f96fbc-7607-4057-83f1-562fce9f6ea5 | 2023-06-08 | Warnings | 98f96fbc-7607-4057-83f1-562fce9f6ea5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
