warnings
Warnings kidney disease a magnesium restricted diet abdorominal pain, nausea, or vomiting noticed a sudden change in bowel habits that persists over a period of 2 weeks already used a laxative for a period longer than 1 week
Magnesium Citrate
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
- Brand name
- Magnesium Citrate
- Generic name
- BE HEALTH MAGNESIUM CITRATE ORAL SOLUTION - CHERRY
- Manufacturer
- Bionpharma, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f0fa4b72-50a5-5c42-e053-2995a90a159a
- SPL ID
- 0cf50dbf-e935-7116-e063-6294a90a5b4e
- Version
- 2
- Effective date
- 2023-12-20
- Source export date
- 2026-10-27
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:03:55
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M007 | openfda.application_number | |
| brand name | Magnesium Citrate | openfda.brand_name | |
| generic name | BE HEALTH MAGNESIUM CITRATE ORAL SOLUTION - CHERRY | openfda.generic_name | |
| manufacturer name | Bionpharma, Inc. | openfda.manufacturer_name | |
| ndc | package | 69452-390-98 | openfda.package_ndc |
| ndc | product | 69452-390 | openfda.product_ndc |
| ndc11 | package | 69452039098 | derived:openfda.package_ndc |
| rxcui | 1052760 | openfda.rxcui | |
| spl id | 0cf50dbf-e935-7116-e063-6294a90a5b4e | id | |
| spl set id | f0fa4b72-50a5-5c42-e053-2995a90a159a | set_id | |
| unii | RHO26O1T9V | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.