HEARTBURN RELIEF

HEARTBURN RELIEF is an FDA drug label for the active ingredient ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE manufactured by CHAIN DRUG MARKETING ASSOCIATION administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231106.

Generic: ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE

Manufacturer: CHAIN DRUG MARKETING ASSOCIATION

Product Type: HUMAN OTC DRUG

Route: ORAL

Dosage Form:

NDC: 63868-565

Application: M001

Effective: 20231106

Active Ingredients: Active ingredients (in each 5 mL teaspoonful) Aluminum hydroxide 254 mg Magnesium carbonate 237.5 mg

Indications & Usage

Uses relieves heartburn sour stomach acid indigestion upset stomach associated with these symptoms

Dosage & Administration

Directions shake well before use adults and children 12 years and older take 2-4 teaspoonsful four times a day or as directed by a doctor children under 12 years: consult a doctor take after meals and at bedtime dispense product only by spoon or other measuring device

Contraindications

Not available.

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.

Adverse Reactions