Aluminum hydroxide and Magnesium carbonate

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
Aluminum hydroxide and Magnesium carbonate
Generic name
ALUMINUM HYDROXIDE, MAGNESIUM CARBONATE
Manufacturer
Simpex Pharma Pvt. Ltd
Product type
HUMAN OTC DRUG
SPL set ID
e799a555-bfd0-4298-a5dc-aeb671815d40
SPL ID
0b5850de-34f4-b95e-e063-6294a90affe1
Version
7
Effective date
2023-11-29
Source export date
2026-10-27
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:56:27
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor before use if you have kidney disease a magnesium or sodium-restricted diet Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 16 tablets in a 24-hour period or use the maximum dosage for more than 2 weeks Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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