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 - GRAPE
- Manufacturer
- Bionpharma, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f0f9ff19-ae08-0af0-e053-2a95a90ab842
- SPL ID
- 0cf518b8-b231-7118-e063-6294a90a391d
- Version
- 2
- Effective date
- 2023-12-20
- Source export date
- 2026-09-28
- 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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:23:54
| 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 - GRAPE | openfda.generic_name | |
| manufacturer name | Bionpharma, Inc. | openfda.manufacturer_name | |
| ndc | package | 69452-391-98 | openfda.package_ndc |
| ndc | product | 69452-391 | openfda.product_ndc |
| ndc11 | package | 69452039198 | derived:openfda.package_ndc |
| rxcui | 1052760 | openfda.rxcui | |
| spl id | 0cf518b8-b231-7118-e063-6294a90a391d | id | |
| spl set id | f0f9ff19-ae08-0af0-e053-2a95a90ab842 | 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.