TIESO SOL UV PROTECTOR

Manufacturer
ATEC CO., LTD. | ANDIVA Inc.
Effective date
2020-08-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:19:06

Label at a glance#

ProductTIESO SOL UV PROTECTOR
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TIESO SOL UV PROTECTORTIESO SOL UV PROTECTOR

Active ingredients Purpose

Ethylhexyl Methoxycinnamate 7.00 %.......................................sunscreen
Ethylhexyl Salicylate 4.80 %......................................................sunscreen

Titanium Dioxide 2.07 %............................................................sunscreen

Inactive ingredients

Chamaecyparis Obtusa Water, Glycerin, Chamaecyparis Obtusa Leaf Extract, Butylene Glycol, Niacinamide, Dicaprylyl Carbonate,
Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Helianthus Tuberosus Extract, 1,2-Hexanediol, Cyclopentasiloxane, Cyclohexasiloxane, Cetearyl Alcohol, Polyglyceryl-3 Methylglucose Distearate, Silica, Lepidium Meyenii Root Extract, Ethyl Hexanediol, Potassium Cetyl Phosphate, Glyceryl Stearate, Stearic Acid, Aloe Barbadensis Leaf Extract, Laminaria Japonica Extract, Dioscorea Japonica Root Extract, Ulmus Davidiana Root Extract, Viola Mandshurica Flower Extract, Aluminum Hydroxide, Ammonium Acryloyldimethyltaurate/VP Copolymer, Glyceryl Caprylate, Water, SodiumAcrylate/Sodium Acryloyldimethyl Taurate Copolymer, Xanthan Gum, Isohexadecane, Adenosine, Dipotassium Glycyrrhizate, Disodium EDTA, Polysorbate 80

OTC - ACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

OTC - WHEN USING SECTION

INACTIVE INGREDIENT SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

INDICATIONS & USAGE SECTION

Products#

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DailyMed product names page 1 of 2 · 41 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69978-005069978-0050-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 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
b55f6037-638f-3cbc-e053-2a95a90a0431aaefd933-ce37-ce3e-e053-2a95a90ac5462020-11-30Exact identifier
spl set id: aaefd933-ce37-ce3e-e053-2a95a90ac546

Reported adverse events (FAERS/openFDA)#

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