FDA.reportPublic FDA data

TIESO RAPIDO

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 23:05:55

Label at a glance#

ProductTIESO RAPIDO
Active ingredientMENTHOL, BENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tieso rapidotieso rapido

Active Ingredients Purposes

Menthol 0.1 %.....................................external analgesic
Benzalkonium chloride 0.04 %...........antibacterial

Inactive ingredients

Water, Alcohol, Triolein, Ethylhexyl Stearate, Lepidium Meyenii Root
Extract, 1,2-Hexanediol, Caprylyl Methicone, Glycerin, Fragrance, Methyl Glucose Sesquistearate, Acrylates/Beheneth-25 Methacrylate Copolymer, Portulaca Oleracea Extract, Xylitylglucoside, Sorbitan Stearate, Anhydroxylitol, Butylene Glycol, Xylitol, Carbomer, Disodium EDTA, Tromethamine, Glucose

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73184-0080-12021-10-22C16284748780-1c7ccaba7-11eb-fd44-e053-dadaa90aa01bTIESO RAPIDO
73184-0080-12021-07-23C16284748780-1c7ccaba7-11eb-fd44-e053-dadaa90aa01bTIESO RAPIDO

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73184-008073184-0080-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
GLYCERYL TRIOLEATEO05EC62663IACT
LEPIDIUM MEYENII ROOTHP7119212TIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
GLYCERINPDC6A3C0OXIACT
XYLITYLGLUCOSIDEO0IEZ166FBIACT
SORBITAN MONOSTEARATENVZ4I0H58XIACT
ANHYDROXYLITOL8XWR7NN42FIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
TROMETHAMINE023C2WHX2VIACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
METHYL GLUCOSE SESQUISTEARATEV1YW10H14DIACT
PURSLANEM6S840WXG5IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
XYLITOLVCQ006KQ1EIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
EDETATE DISODIUM7FLD91C86KIACT
MENTHOLL7T10EIP3AACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ceea01a2-e6fb-9948-e053-2995a90a9e26b4c2a81b-c0aa-50b6-e053-2a95a90a4d7a2021-10-22Exact identifier
spl set id: b4c2a81b-c0aa-50b6-e053-2a95a90a4d7a

Reported adverse events (FAERS/openFDA)#

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