FDA.reportPublic FDA data

Zantanew Tab

Manufacturer
Cho A Pharm Co.,Ltd
Effective date
2023-12-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:19:03

Label at a glance#

ProductZantanew Tab
Active ingredientSILODRATE ANHYDROUS, MAGNESIUM OXIDE
Label structure10 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Ask a doctor or pharmacist before use if you are taking a prescription
drug. Antacids may interact with certain prescription drugs.

warningswarnings

DOSAGE & ADMINISTRATION SECTION

dosagedosage

INDICATIONS & USAGE SECTION

■ heartburn ■ sour stomach ■ acid indigestion ■ upset stomach associated with these symptoms

indicationindication

OTC - ACTIVE INGREDIENT SECTION

Magnesium Aluminosilicate
Magnesium Oxide(Heavy)

active ingredientactive ingredient

OTC - DO NOT USE SECTION

■ children under 12 years of age : do not use
■ adults over 80 yeas old: do not use
■ for oral use only

do not usedo not use

OTC - WHEN USING SECTION

■ do not take more than 6 tablets in 24 hours
■ do not use the maximum dosage for more than 2 weeks
■ do not take tetracyclines antibiotic
■ do not take alcohol

when usingwhen using

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help of contact a Poison Control Center right away.

keep out of reach of childrenkeep out of reach of children

OTC - PURPOSE SECTION

purposepurpose

INACTIVE INGREDIENT SECTION

inactive ingredientinactive ingredient

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

display paneldisplay panel

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
58354-20158354-201-02

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
SILODRATE ANHYDROUS59110L5W24ACTIB
MAGNESIUM OXIDE3A3U0GI71GACTIM
CROSPOVIDONE2S7830E561IACT
MAGNESIUM STEARATE70097M6I30IACT
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED2165RE0K14IACT

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
1b8bcfa8-7f8c-8423-e063-6394a90a58dd07806e4b-9125-a533-e063-6394a90a16fc2024-06-23WarningsExact identifier
spl set id: 07806e4b-9125-a533-e063-6394a90a16fc

Reported adverse events (FAERS/openFDA)#

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