ACTIVE INGREDIENT
ACTIVE INGREDIENTS: Titanium Dioxide (CI 77891) (10.9%) - SUNSCREEN Ethylhexyl Methoxycinnamate (6.7%) - SUNSCREEN Ethylhexyl Salicylate (4%) - SUNSCREEN
NATURE ORIGIN CUSHION CC NATURAL
- Manufacturer
- NATURE REPUBLIC CO., LTD. | Cosmax, Inc.
- Effective date
- 2019-12-31
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:47:28
Label at a glance#
ProductNATURE ORIGIN CUSHION CC NATURAL NO.23
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT
INACTIVE INGREDIENTS: Water, Cyclopentasiloxane, Butylene Glycol, Caprylyl Methicone, PEG-10 Dimethicone, Glycerin, Niacinamide, Diphenylsiloxy Phenyl Trimethicone, Butylene Glycol Dicaprylate/Dicaprate, Pentylene Glycol, PEG-8 Dimethicone, Dimethicone, Iron Oxides (CI 77492), PEG-8, HDI/Trimethylol Hexyllactone Crosspolymer, Mica (CI 77019), Phenoxyethanol, Magnesium Sulfate, Diphenyl Dimethicone, Acrylates/Stearyl Acrylate/Dimethicone Methacrylate Copolymer, Trimethylsiloxysilicate, Dimethicone Crosspolymer, Cyclohexasiloxane, Stearic Acid, Disteardimonium Hectorite, Alumina, Iron Oxides (CI 77491), Dimethicone/Vinyl Dimethicone Crosspolymer, Fragrance(Parfum), Triethoxycaprylylsilane, Aluminum Hydroxide, Iron Oxides (CI 77499), Ethylhexylglycerin, Adenosine, Disodium EDTA, Silica,Ceramide 3, Ascorbic Acid, Soluble Collagen
PURPOSE
SUNSCREEN
WARNINGS
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. After use, close the cap tightly to prevent the product from degradation and evaporation.
KEEP OUT OF REACH OF CHILDREN
KEEP OUT OF REACH OF CHILDREN
INDICATIONS & USAGE
HOW TO USE : Take an adequate amount by gently pressing the sponge with the puff, and apply thinly to the face. Gently pat to adhere to the skin. Apply as needed after wearing makeup.
DOSAGE & ADMINISTRATION
HOW TO USE : Take an adequate amount by gently pressing the sponge with the puff, and apply thinly to the face. Gently pat to adhere to the skin. Apply as needed after wearing makeup.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 8806173417568 | GTIN-13: 8806173417568 EAN-13: 8806173417568 GTIN storage (14 digits): 08806173417568 | cc natural carton.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51346-272-01 | 2021-07-13 | C162847 | 48780-1 | ba0f9c33-176d-a910-e053-dadaa90a0b85 | 3bd4030f-2958-428d-b339-d8db75246e34 |
| 51346-272-01 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-176d-a910-e053-dadaa90a0b85 | 3bd4030f-2958-428d-b339-d8db75246e34 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| OCTINOXATE | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| OCTISALATE | ACTIVE INGREDIENT | 4X49Y0596W | 1 | |
| TITANIUM DIOXIDE | ACTIVE INGREDIENT | 15FIX9V2JP | 1 | |
| OCTINOXATE | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| OCTISALATE | ACTIVE MOIETY | 4X49Y0596W | 1 | |
| TITANIUM DIOXIDE | ACTIVE MOIETY | 15FIX9V2JP | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- NATURE ORIGIN CUSHION CC NATURAL NO.23
- TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
- TITANIUM DIOXIDE
- OCTINOXATE
- OCTISALATE
- Water
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51346-272 | 51346-272-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TITANIUM DIOXIDE | 15FIX9V2JP | ACTIB |
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| Water | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| 4bfd5f08-8262-4763-9636-9bac265c0f95 | 3bd4030f-2958-428d-b339-d8db75246e34 | 2021-07-13 | Warnings | 3bd4030f-2958-428d-b339-d8db75246e34 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.