LUMINOUS GODDESS AURA BB

Manufacturer
TONYMOLY CO., LTD. | COSMAX INC.
Effective date
2015-02-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:41:51

Label at a glance#

ProductLUMINOUS GODDESS AURA BB
Active ingredientTitanium Dioxide, OCTINOXATE, Zinc Oxide
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Titanium Dioxide 9.94%, Ethylhexyl Methoxycinnamate 7.00%, Zinc Oxide 2.94%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Cyclopentasiloxane, Dipropylene Glycol, Butylene Glycol Dicaprylate/Dicaprate, Phenyl Trimethicone, Cyclohexasiloxane, Cetyl PEG/PPG-10/1 Dimethicone, Arbutin, Hexyldecyl Myristoyl Methylaminopropionate, Hexyl Laurate, Magnesium Sulfate, Sorbitan Sesquioleate, Silica, Iron Oxides (CI 77492), Disteardimonium Hectorite, Isoamyl p-Methoxycinnamate, Tribehenin, Iron Oxides (CI 77491), Aluminum Hydroxide, Methylparaben, Chlorphenesin, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Iron Oxides (CI 77499), Stearic Acid, Triethoxycaprylylsilane, Glyceryl Behenate, Calcium Stearate, Polyglyceryl-6 Octastearate, Propylparaben, Fragrance(Parfum), Dimethicone, Disodium EDTA, Butylene Glycol, Adenosine, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Hydrolyzed Coral, Borago Officinalis Seed Oil, Bertholletia Excelsa Seed Oil, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Argania Spinosa Kernel Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Centella Asiatica Extract, Caffeine, Hydrolyzed Collagen, Rosa Damascena Flower Oil, Rosa Gallica Flower Extract, Camellia Sinensis Leaf Extract, Arnica Montana Flower Extract, Jasminum Officinale (Jasmine) Flower Extract, Portulaca Oleracea Extract, Achillea Millefolium Extract, Pearl Powder, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Sodium Hyaluronate, Palmitoyl Tripeptide-5

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. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) 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 babies and children

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

INDICATIONS AND USAGE: Mix Luminous Goddess Aura Beam and Luminous Goddess Aura BB Cream 1:2 Ratio and tap it to whole face lightly.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59078-042-012020-01-31C16284748780-19d75b9d0-cbb6-f424-e053-dadaa90a57ce3bab6005-1de7-4cc4-8869-17a748db2e80

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59078-042-01LUMINOUS GODDESS AURA BB45 g in 1 CARTONCREAM453

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59078-042LUMINOUS GODDESS AURA BB (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE) CREAM [TONYMOLY CO., LTD.]3Legacy NDC, 1 package rows20150227_3bab6005-1de7-4cc4-8869-17a748db2e80.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD513
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP3
Zinc OxideACTIVE INGREDIENTSOI2LOH54Z3
OCTINOXATEACTIVE MOIETY4Y5P7MUD513
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP3
ZINC CATIONACTIVE MOIETY13S1S8SF373
Dipropylene GlycolINACTIVE INGREDIENTE107L85C403
WaterINACTIVE INGREDIENT059QF0KO0R3

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
59078-04259078-042-01

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

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates

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
76c21478-3b83-4071-b4f7-a0bd20d800a73bab6005-1de7-4cc4-8869-17a748db2e802015-02-27WarningsExact identifier
spl id: 76c21478-3b83-4071-b4f7-a0bd20d800a7
spl set id: 3bab6005-1de7-4cc4-8869-17a748db2e80

Reported adverse events (FAERS/openFDA)#

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