MINTOX MAXIMUM STRENGTH

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
MINTOX MAXIMUM STRENGTH
Generic name
ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE
Manufacturer
ATLANTIC BIOLOGICALS CORP.
Product type
HUMAN OTC DRUG
SPL set ID
ac6a47e7-972f-4b82-96da-89926d345e9f
SPL ID
3b3f429e-d2e4-441c-e063-6294a90aaf4d
Version
9
Effective date
2025-07-31
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:31
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 Ask a doctor before use if you have • kidney disease • a magnesium-restricted diet taking a prescription drug. Ask a doctor or pharmacist before use if you are Antacids may interact with certain prescription drugs. symptoms last more than 2 weeks Stop use and ask a doctor if ask a health professional before use. If pregnant or breast-feeding, Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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