FDA.reportPublic FDA data

FULL STAY CC 24 HR SUNSCREEN CREAM V201 APRICOT BEIGE SPF 50 34200406

Manufacturer
THEFACESHOP CO., LTD. | THEFACESHOP NORTH AMERICA, INC.
Effective date
2015-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:43:44

Label at a glance#

ProductFULL STAY CC 24HR
Active ingredientTITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE, OCTINOXATE
Label structure10 sections

Indications and uses

Helps prevent sunburn.

Dosage and administration

Apply generously and evenly 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor. Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating. Open the produc...

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.0 %
Octisalate 4.5 %
Titanium Dioxide 13.4 %
Zinc Oxide 4.9 %

Purpose

OTC - PURPOSE SECTION

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Uses:

OTC - PURPOSE SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

OTC - WHEN USING SECTION

Apply generously and evenly 15 minutes before sun exposure.
Children under 6 months of age: Ask a doctor.
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
Reapply at least every 2 hours.
Use a water-resistant sunscreen if swimming or sweating.

Open the product and press the button in front once or twice. Dispense an adequate amount on the puff and apply all over the face. Finish with a patting motion. If contents does not dispense well after the button is pressed, shake the product gently and try again. Press the button carefully not to spurt contents.

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.

May stain or damage some fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Cyclopentasiloxane, Butylene Glycol Dicaprylate/Dicaprate, Dicaprylyl Carbonate, Glycerin, Niacinamide, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Pentylene Glycol, Methyl Methacrylate Crosspolymer, Phenyl Trimethicone, Iron Oxides (CI 77492), Butylene Glycol, Disteardimonium Hectorite, Cetyl PEG/PPG-10/1 Dimethicone, Sodium Chloride, Caprylyl Methicone, Dimethicone, Tribehenin, Aluminum Hydroxide, Sorbitan Isostearate, Phenoxyethanol, Glyceryl Tribehenate/Isostearate/Eicosandioate, Stearic Acid, Dimethicone Crosspolymer, Triethoxycaprylylsilane, Dimethicone/Vinyl Dimethicone Crosspolymer, Ethylhexylglycerin, Adenosine, Hydrogenated Castor Oil Isostearate, Disodium EDTA, Lauroyl Lysine, HDI/Trimethylol Hexyllactone Crosspolymer, Rosa Damascena Flower Water, Silica, Pancratium Maritimum Extract, Fragrance, Mica (CI 77019), Iron Oxides (CI 77491, CI 77492, CI 77499)

OTC - QUESTIONS SECTION

Questions or comments? Call 1-866-638-8417

Distributed by:

SPL UNCLASSIFIED SECTION

THEFACESHOP NORTH AMERICA, INC.

Santa Fe Springs, CA 90670

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FULL STAY CC

24HR SUNSCREEN CREAM

V201 APRICOT BEIGE SPF 50+ PA+++

All-in-one CC leaves skin looking smooth and flawless for hours

with triple benefits of moisture + coverage + adherence and real brightening effect.

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-406-312020-01-31C16284748780-19d75b9d0-20f5-f424-e053-dadaa90a57ceFULL STAY CC 24 HR SUNSCREEN CREAM V201 APRICOT BEIGE SPF 50 34200406

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-406-31FULL STAYCC 24HR1 in 1 CARTONCREAM11
51523-406-31FULL STAYCC 24HR16 g in 1 CONTAINERCREAM161

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-406FULL STAY CC 24HR (OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE CREAM) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20151001_20d1e07d-b7dc-6ebb-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51523-40651523-406-31

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTISALATE4X49Y0596WACTIB
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
OCTINOXATE4Y5P7MUD51ACTIB

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
20d1e07d-b7dd-6ebb-e054-00144ff8d46c20d1e07d-b7dc-6ebb-e054-00144ff8d46c2015-09-28WarningsExact identifier
spl id: 20d1e07d-b7dd-6ebb-e054-00144ff8d46c
spl set id: 20d1e07d-b7dc-6ebb-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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