ACTIVE INGREDIENT
Active Ingredients:Titanium Dioxide 10.23%, Ethylhexyl Methoxycinnamate 7.50%, Zinc Oxide 7.25%
SUPER ORIGIN CUSHION COMPLETE CONTROL
- Manufacturer
- NATURE REPUBLIC CO., LTD.
- Effective date
- 2014-04-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:36:26
Label at a glance#
ProductSUPER ORIGIN CUSHION COMPLETE CONTROL 23 MOIST AND NATURAL SKIN
Active ingredientTitanium Dioxide, OCTINOXATE, Zinc Oxide
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT
Inactive Ingredients:
Water, Cyclopentasiloxane, C12-15 Alkyl benzoate, Dipropylene Glycol, 4-Methylbenzylidene Camphor, Dimethicone, Phenyl trimethicone, PEG-10 Dimethicone, PEG-9 Polydimethylsiloxyethyl, Dimethicone, Niacinamide, Methicone, Dimethicone/PEG-10/15 Crosspolymer,
CI 77492, Disteardimonium Hectorite, Silica, Dimethicone Methicone Copolymer, Acrylates/Dimethicone Copolymer, CI 77491, Phenoxyethanol, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer,
CI 77499, Ultramarines, Disodium EDTA, Hydrogen Dimethicone, Parfum, Hydrolyzed Collagen, Triethoxycaprylylsilane, Butylene Glycol, Ceramide 3, Magnesium Ascorbyl Phosphate
PURPOSE
Purpose: UV Protection, Brightening
Cautions
Cautions:
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.
Make sure to close the lid tightly to prevent spoilage and shrinkage of the contents.
KEEP OUT OF REACH OF CHILDREN
KEEP OUT OF REACH OF CHILDREN
How to Use
How to Use:
At the step for applying sun cream, evenly apply to the skin using the puff, and gently pat to enhance absorption into the skin.
Reapply throughout the day as needed.
How to Use
How to Use:
At the step for applying sun cream, evenly apply to the skin using the puff, and gently pat to enhance absorption into the skin.
Reapply throughout the day as needed.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 8806173402656 | GTIN-13: 8806173402656 EAN-13: 8806173402656 GTIN storage (14 digits): 08806173402656 | super origin cushion complete control carton.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51346-260-01 | 2020-02-14 | C162847 | 48780-1 | 9d75b9d0-d38a-f424-e053-dadaa90a57ce | 3f6c772f-b2b8-45fe-88a0-3731dd98b262 |
| 51346-260-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-d38a-f424-e053-dadaa90a57ce | 3f6c772f-b2b8-45fe-88a0-3731dd98b262 |
DailyMed Socrata Ingredients#
| 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 | |
| C12-15 Alkyl benzoate | INACTIVE INGREDIENT | A9EJ3J61HQ | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- SUPER ORIGIN CUSHION COMPLETE CONTROL 23 MOIST AND NATURAL SKIN
- Titanium Dioxide, OCTINOXATE, Zinc Oxide
- Titanium Dioxide
- OCTINOXATE
- Zinc Oxide
- ZINC CATION
- Water
- C12-15 Alkyl benzoate
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51346-260 | 51346-260-01 |
Ingredients#
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 |
| C12-15 Alkyl benzoate | A9EJ3J61HQ | 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 |
|---|---|---|---|---|---|---|
| 7542d7f6-742e-443d-ad75-6fc5b450683b | 3f6c772f-b2b8-45fe-88a0-3731dd98b262 | 2014-04-30 | Warnings | 7542d7f6-742e-443d-ad75-6fc5b450683b 3f6c772f-b2b8-45fe-88a0-3731dd98b262 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.