rootree Mobitherapy UV Sun Shield

Manufacturer
KTCS Corporation | ATEC Co., Ltd.
Effective date
2020-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:16

Label at a glance#

Productrootree Mobitherapy UV Sun Shield
Active ingredientOctinoxate, Octisalate, Titanium Dioxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 7.0%
Ethylhexyl Salicylate 4.80%
Titanium Dioxide 2.075%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Glycerin, Dicaprylyl Carbonate, Niacinamide, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Cyclopentasiloxane, Cyclohexasiloxane, Glyceryl Stearate, Stearic Acid, Potassium Cetyl Phosphate, Arachidyl Alcohol, Polysorbate 60, Dimethicone, PEG-100 Stearate, Polymethyl Methacrylate, Behenyl Alcohol, Dimethicone/ Vinyl Dimethicone Crosspolymer, Ammonium Acryloyldimethyltaurate/VP Copolymer, Caprylyl Glycol, Aluminum Hydroxide, Arachidyl Glucoside, Fragrance, Xanthan Gum, Arginine, Caprylhydroxamic Acid, Carbomer, Adenosine, Sesamum Indicum (Sesame) Sprout Extract, Glycine Soja (Soybean) Sprout Extract, Phaseolus Radiatus Sprout Extract, Lactobacillus Ferment Lysate, Dendropanax Morbifera Extract, Mentha Arvensis Leaf Extract, Brassica Napus Extract, Citrus Sudachi Fruit Juice, Dipotassium Glycyrrhizate, Disodium EDTA, Tocopheryl Acetate, Benzyl Alcohol, Centella Asiatica Extract

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

WARNINGS

WARNINGS SECTION

- Cease use if problems arise after applying the product and consult a specialist on the symptoms

- Do not use on the wound

- Keep the product out of the reach of children and avoid storing in are as exposed to direct sunlight

DESCRIPTION

DESCRIPTION SECTION

Uses:

It is a natural sun-cream product containing the ingredients extracted from Dendropanax Mobifera tree of Jeju. Its natural formulation protects skin from the UV ray A and B which cause skin-aging. It softly embraces skin with long lasting moisture and forwards rich natural moisturizing ingredients to your skin.

Directions:

At the last stage of basic skin care, apply the adequate amount on the areas such as face, neck, arms, legs and etc. which can be easily exposed to UV rays.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72441-070-022021-07-23C16284748780-1c7ccaba7-2af6-fd44-e053-dadaa90aa01bc02c9385-21b8-4d80-bbdc-e1587aca2a51

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72441-070-01rootree Mobitherapy UV Sun Shield60 g in 1 CONTAINERCREAM602
72441-070-02rootree Mobitherapy UV Sun Shield1 in 1 CARTONCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72441-070ROOTREE MOBITHERAPY UV SUN SHIELD (OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE) CREAM [KTCS CORPORATION]2Legacy NDC, 2 package rows20201231_c02c9385-21b8-4d80-bbdc-e1587aca2a51.zip

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
72441-07072441-070-01, 72441-070-02

Ingredients#

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

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

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
112bf256-6d27-4ea6-a94d-bf49ad9353b1c02c9385-21b8-4d80-bbdc-e1587aca2a512020-12-31WarningsExact identifier
spl id: 112bf256-6d27-4ea6-a94d-bf49ad9353b1
spl set id: c02c9385-21b8-4d80-bbdc-e1587aca2a51

Reported adverse events (FAERS/openFDA)#

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