ACTIVE INGREDIENT
Active Ingredients: Titanium Dioxide 9.94%, Ethylhexyl Methoxycinnamate 7.00%, Zinc Oxide 2.94%
Active Ingredients: Titanium Dioxide 9.94%, Ethylhexyl Methoxycinnamate 7.00%, Zinc Oxide 2.94%
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, Iron Oxides (CI 77492), Sorbitan Sesquioleate, Magnesium Sulfate, Phenoxyethanol, Disteardimonium Hectorite, Isoamyl p-Methoxycinnamate, Silica, Iron Oxides (CI 77491), Tribehenin, Iron Oxides (CI 77499), Aluminum Hydroxide, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Stearic Acid, Triethoxycaprylylsilane, Glyceryl Behenate, Calcium Stearate, Polyglyceryl-6 Octastearate, Fragrance(Parfum), Ethylhexylglycerin, Dimethicone, Disodium EDTA, Adenosine, Water, Butylene Glycol, Ceramide 3, Tremella Fuciformis (Mushroom) Extract, Mica (CI 77019), Glycerin, Melissa Officinalis Leaf Extract, Malva Sylvestris (Mallow) Extract, Achillea Millefolium Extract, Alchemilla Vulgaris Extract, Primula Veris Extract, Mentha Piperita (Peppermint) Leaf Extract, Veronica Officinalis Extract, Ethyl Hexanediol, Oxygen
Purpose: Sunscreen
Warning: 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: Keep out of reach of babies and children
Indication & Usage: After application of skin care products, apply on face using fingertips or sponge.
Dosage & Administration: Take an adequate amount of this product.
Image of carton
| Class | Version | Type | Effective |
|---|---|---|---|
| ZINC CATION Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 59078-052-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-0298-f424-e053-dadaa90a57ce | bd99a8f7-6300-4d6d-b3ab-f301b3278e16 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59078-052-01 | TONYMOLY LUMINOUS GODDESS AURA BB02 | 45 g in 1 CARTON | CREAM | 45 | 1 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Octinoxate | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| Titanium Dioxide | ACTIVE INGREDIENT | 15FIX9V2JP | 1 | |
| Zinc Oxide | ACTIVE INGREDIENT | SOI2LOH54Z | 1 | |
| OCTINOXATE | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| TITANIUM DIOXIDE | ACTIVE MOIETY | 15FIX9V2JP | 1 | |
| ZINC CATION | ACTIVE MOIETY | 13S1S8SF37 | 1 | |
| Dipropylene Glycol | INACTIVE INGREDIENT | E107L85C40 | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 59078-052 | 59078-052-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Titanium Dioxide | 15FIX9V2JP | ACTIB |
| Octinoxate | 4Y5P7MUD51 | ACTIB |
| Zinc Oxide | SOI2LOH54Z | ACTIM |
| Water | 059QF0KO0R | IACT |
| Dipropylene Glycol | E107L85C40 | IACT |
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| Dipropylene Glycol | DIPROPYLENE GLYCOL | E107L85C40 | FILM, EXTENDED RELEASE / TRANSDERMAL | 296 mg | ||
| Dipropylene Glycol | DIPROPYLENE GLYCOL | E107L85C40 | SYSTEM / TRANSDERMAL | 6 mg | ||
| Dipropylene Glycol | DIPROPYLENE GLYCOL | E107L85C40 | FILM, EXTENDED RELEASE / BUCCAL | 30 mg |
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 |
|---|---|---|---|---|---|---|
| 8220f498-5457-4241-8dd2-1aa3c1733e68 | bd99a8f7-6300-4d6d-b3ab-f301b3278e16 | 2015-03-03 | Warnings | 8220f498-5457-4241-8dd2-1aa3c1733e68 bd99a8f7-6300-4d6d-b3ab-f301b3278e16 |
Adverse event summaries are temporarily unavailable. Other product information remains available.