ACTIVE INGREDIENT
Active Ingredient: Magnolia Kobus Flower Extract 14.56%
Active Ingredient: Magnolia Kobus Flower Extract 14.56%
Inactive Ingredients:
Purified water, Orostachys Japonica Extract, Ginkgo Biloba Leaf Extract, Cnidium Officinale Rhizome Extract, Poria Cocos Extract, Gardenia Florida Flower Extract, Paeonia Suffruticosa Root Extract, Dandelion Leaf Extract, Morus Alba Leaf Extract,
Houttuynia Cordata Extract, Arbutin, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Ferment Extract, Coffee Robusta Seed Extract, Lavander Oil
Purpose: Skin Brightening
Warnings:
For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace the cap after use.
KEEP OUT OF REACH OF CHILDREN
How to use:
Pat on your face right after cleansing in the morning and in the evening. This whitening serum brightens and monetarizes naturally for radiant looking.
How to use:
Pat on your face right after cleansing in the morning and in the evening. This whitening serum brightens and monetarizes naturally for radiant looking.
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70800-100-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-351c-a910-e053-dadaa90a0b85 | 3a03770f-a088-4ad1-836c-15c654ea4844 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70800-100-01 | Magnolia Serum | 30 mL in 1 BOTTLE, GLASS | LIQUID | 30 | 2 | |
| 70800-100-02 | Magnolia Serum | 1 in 1 CARTON | LIQUID | 1 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 70800-100 | 70800-100-01, 70800-100-02 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MAGNOLIA KOBUS FLOWERING TOP | X2725LP5TL | ACTIB |
| Water | 059QF0KO0R | IACT |
| Arbutin | C5INA23HXF | 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 |
|---|---|---|---|---|---|---|
| 0faffbc2-b035-4483-9c10-39b676a19167 | 3a03770f-a088-4ad1-836c-15c654ea4844 | 2019-12-10 | Warnings | 0faffbc2-b035-4483-9c10-39b676a19167 3a03770f-a088-4ad1-836c-15c654ea4844 |
Adverse event summaries are temporarily unavailable. Other product information remains available.