FDA.reportPublic FDA data

HEARTBURN RELIEF

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

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

Brand name
HEARTBURN RELIEF
Generic name
ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE
Manufacturer
GERI-CARE PHARMACEUTICALS, CORP
Product type
HUMAN OTC DRUG
SPL set ID
1f1dbf41-cb87-37d4-e063-6394a90ae294
SPL ID
28d955ae-eec6-64fc-e063-6294a90a154d
Version
2
Effective date
2024-12-09
Source export date
2026-08-01
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/2026-08-01/29baabee7fa6726d72190670d84f1571113181a958a8119cbe97e8f0d1d955b2/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:13:55
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 laxative effect may occur do not use maximum dosage for more than 2 weeks do not take more than 16 teaspoonfuls in 24 hours If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.