FDA.reportPublic FDA data

TIESO RAPIDO PLUS

Manufacturer
ANDIVA Inc. | ATEC CO., LTD.
Effective date
2020-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:05:57

Label at a glance#

ProductTIESO RAPIDO PLUS
Active ingredientHOMOSALATE, BENZALKONIUM CHLORIDE, TITANIUM DIOXIDE, OCTISALATE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purposes

Homosalate 5.00 % .......................................... sunscreen
Ethylhexyl Salicylate 4.5% .................................sunscreen
Titanium Dioxide 2.1 % ......................................sunscreen
Benzalkonium Chloride 0.04 % .......................antibacterial

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, Dicaprylyl Carbonate, Alcohol, Cyclomethicone, Phenylbenzimidazole Sulfonic Acid, Lepidium Meyenii Root Extract, Glycerin, 1,2-Hexanediol, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Diethylamino Hydroxybenzoyl Hexyl Benzoate, C13-16 Isoparaffin, PEG-10 Dimethicone, Sodium Chloride, Heptyl Undecylenate, Sodium Hydroxide, Aloe Barbadensis Leaf Extract, Dioscorea Japonica Root Extract, Laminaria Japonica Extract, Ulmus Davidiana Root Extract, Viola Mandshurica Flower Extract, Stearic acid, Aluminum Hydroxide, Butylene Glycol, Disodium EDTA, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TIESO RAPIDO PLUSTIESO RAPIDO PLUS

OTC - ASK DOCTOR SECTION

OTC - STOP USE SECTION

OTC - DO NOT USE SECTION

OTC - PURPOSE SECTION

OTC - WHEN USING SECTION

INDICATIONS & USAGE SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

OTHER SAFETY INFORMATION

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73184-008273184-0082-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
LEPIDIUM MEYENII ROOTHP7119212TIACT
WATER059QF0KO0RIACT
CYCLOMETHICONENMQ347994ZIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
DIOSCOREA JAPONICA ROOTI43FCF3356IACT
VIOLA MANDSHURICA FLOWER46MR945M6XIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
ENSULIZOLE9YQ9DI1W42IACT
C13-16 ISOPARAFFINLED42LZG6OIACT
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20IACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM HYDROXIDE55X04QC32IIACT
LAMINARIA JAPONICAWE98HW412BIACT
EDETATE DISODIUM7FLD91C86KIACT
STEARIC ACID4ELV7Z65APIACT
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
BEMOTRIZINOLPWZ1720CBHIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
HEPTYL UNDECYLENATEW77QUB6GXOIACT
ALOE VERA LEAFZY81Z83H0XIACT
ULMUS DAVIDIANA ROOTURQ79U8261IACT
HOMOSALATEV06SV4M95SACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTISALATE4X49Y0596WACTIB

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
b55f9cbe-4f4b-9669-e053-2995a90a6a04b4c30172-9fb2-3add-e053-2a95a90a0c992020-11-30Exact identifier
spl set id: b4c30172-9fb2-3add-e053-2a95a90a0c99

Reported adverse events (FAERS/openFDA)#

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