Magnesia sulphurica
MAGNESIUM SULFATE HEPTAHYDRATE
ORAL
HUMAN OTC DRUG
Magnesia sulphurica is an FDA drug label for the active ingredient MAGNESIUM SULFATE HEPTAHYDRATE manufactured by Boiron 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 20231114.
- Generic name
- MAGNESIUM SULFATE HEPTAHYDRATE
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-3267
- Application
- N/A
- Label effective
- 20231114
Active ingredients
Magnesia sulphurica 30C (**contains 0.443 mg of the active ingredient per pellet)
Indications & Usage
Irritability or itchy skin rash*
Dosage & Administration
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Contraindications
Not available.
Warnings
Not available.
Adverse Reactions
Not available.