ACID GONE ANTACID

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
ACID GONE ANTACID
Generic name
ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE
Manufacturer
Major Pharmaceuticals
Product type
HUMAN OTC DRUG
SPL set ID
3d353a92-92f1-4304-8895-31d39dccd88c
SPL ID
5333826a-ab01-5e1b-e063-6394a90ac59e
Version
5
Effective date
2026-06-01
Source export date
2026-11-06
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/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:43:30
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 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. When using this product do not take more than 8 tablespoonfuls in 24 hours do not use the maximum dosage for more than 2 weeks laxative effect may occur If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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