INON

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
INON
Generic name
ALUMINUM HYDROXIDE, MAGNESIUM CARBONATE, SODIUM BICARBONATE
Manufacturer
Sato Pharmaceutical Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
e86d9c57-c877-49f1-a405-95a9a226ccf3
SPL ID
0bb8901e-89d2-b026-e063-6294a90ae77a
Version
4
Effective date
2023-12-04
Source export date
2026-10-30
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:02:29
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings If pregnant or breast-feeding , ask a health professional before use. When using this product ■ Do not take more than 3 packets in 24-hours period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor ■ May have laxative effect Ask a doctor before use if you have ■ a sodium-restricted diet Ask a doctor or pharmacist before use if you are ■ taking a prescription drug Antacids may interact with certain prescription drugs. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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