ACTIVE INGREDIENT
Active ingredients: Titanium Dioxide 6.20%, Ethylhexyl Methoxycinnamate 4.00%, Zinc Oxide 1.96%
Active ingredients: Titanium Dioxide 6.20%, Ethylhexyl Methoxycinnamate 4.00%, Zinc Oxide 1.96%
Inactive ingredients:
Talc, Mica (CI 77019), Silica, Nylon-12, Triethylhexanoin, Magnesium Myristate, Trimethylolpropane Triethylhexanoate, Methyl Methacrylate Crosspolymer, Triethoxycaprylylsilane, Iron Oxides (CI 77492), Dimethicone, Caprylyl Glycol, Ethylhexylglycerin, Methicone, Iron Oxides (CI 77491), Hydrogenated Lecithin, Fragrance(Parfum), Lauroyl Lysine, Iron Oxides (CI 77499), Ultramarines (CI 77007), Tocopheryl Acetate, Betula Platyphylla Japonica Juice, Water, Rosa Centifolia Flower Water, Butylene Glycol
Purpose: Sunscreen
Warnings:
For external use only
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.
4. Keep out of reach of babies and children.
Uses:
Helps prevent sunburn.
Directions:
Apply appropriate amount on a puff and gently apply on the entire face followed by skin texture, tap lightly to finish.
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 70341-626 | 70341-626-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Titanium Dioxide | 15FIX9V2JP | ACTIB |
| Octinoxate | 4Y5P7MUD51 | ACTIB |
| Zinc Oxide | SOI2LOH54Z | ACTIM |
| Talc | 7SEV7J4R1U | IACT |
| Mica | V8A1AW0880 | IACT |
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 |
|---|---|---|---|---|---|---|
| f0ecf9a5-7886-4075-bd6e-d7732c7f2ab7 | 6918da18-a515-4ece-89a9-3ff824d87705 | 2019-12-30 | Warnings | 6918da18-a515-4ece-89a9-3ff824d87705 |
Adverse event summaries are temporarily unavailable. Other product information remains available.