FDA.reportPublic FDA data

SIERO CO AQUA CUSHION FOUNDATION 21 NATURAL BEIGE

Manufacturer
JNG KOREA CO.,LTD. | Hankook Cosmetics Manufacturing Co.,Ltd_Eumseong Factory
Effective date
2017-06-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:22

Label at a glance#

ProductSIERO CO AQUA CUSHION FOUNDATION 21 NATURAL BEIGE
Active ingredientTitanium Dioxide, Octinoxate, Octisalate, Octocrylene, Zinc Oxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 9.0%, Ethylhexyl Methoxycinnamate 7.0%, Ethylhexyl Salicylate 4.8%, Octocrylene 2.0%, Zinc Oxide 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water,Cyclopentasiloxane,Cyclohexasiloxane,Glycerin,C12-15 Alkyl benzoate,PEG-30 Dipolyhydroxystearate, Butylene Glycol Dicaprylate/Dicaprate,Niacinamide,PEG-10 Dimethicone,CI 77492,Butylene Glycol,Quaternium-18 Bentonite,Sodium Chloride,Dimethicone,Copernicia Cerifera (Carnauba) Wax,Ozokerite,CI 77491,Chlorphenesin,Triethoxycaprylylsilane,Aluminum Hydroxide,Parfum,CI 77499,Adenosin,Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer,Rosa Damascena Flower Water,Nelumbo Nucifera Flower Extract,Calendula Officinalis Flower Extract,Angelica Archangelica Root Extract,Phenoxyethanol,Viola Tricolor Extract,Sodium Hyaluronate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: - Keep away from direct sunlight and high temperature. - For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use.

Keep Out of Reach of Children

DESCRIPTION

DESCRIPTION SECTION

Uses: Moisture bomb cushion that gives a rich and moisturizing feeling providing skin moisture and radiance. It contains hyaluronic acid, lotus extract, calendula flower extract, pansy extract, angelica root extract, and damask rose flower water, replenishing moisture from the moment you apply providing healthy radiant skin.

Directions: Apply a moderate amount to the puff and dab it over the entire face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71472-040-022024-12-03C16284748780-19d75b9d1-0f54-f424-e053-dadaa90a57cebe1e982d-9bb1-450f-a9cc-510c6fc19e1e
71472-040-022020-01-31C16284748780-19d75b9d1-0f54-f424-e053-dadaa90a57cebe1e982d-9bb1-450f-a9cc-510c6fc19e1e

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71472-04071472-040-01, 71472-040-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
Titanium Dioxide15FIX9V2JPACTIB
Octinoxate4Y5P7MUD51ACTIB
Octisalate4X49Y0596WACTIB
Octocrylene5A68WGF6WMACTIB
Zinc OxideSOI2LOH54ZACTIM
Water059QF0KO0RIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
285a6601-8d8b-5e7c-e063-6394a90ae9f7be1e982d-9bb1-450f-a9cc-510c6fc19e1e2024-12-03WarningsExact identifier
spl set id: be1e982d-9bb1-450f-a9cc-510c6fc19e1e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.