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
- CVS MAGNESIUM CITRATE ORAL SOLUTION - GRAPE
- Manufacturer
- CVS Pharmacy, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- fb808dc5-bf80-836c-e053-6294a90a80aa
- SPL ID
- 2a807f1b-9870-a9ea-e063-6394a90aed25
- Version
- 2
- Effective date
- 2024-12-30
- Source export date
- 2026-11-06
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:46:46
| 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 | CVS MAGNESIUM CITRATE ORAL SOLUTION - GRAPE | openfda.generic_name | |
| manufacturer name | CVS Pharmacy, Inc. | openfda.manufacturer_name | |
| ndc | package | 51316-881-10 | openfda.package_ndc |
| ndc | product | 51316-881 | openfda.product_ndc |
| ndc11 | package | 51316088110 | derived:openfda.package_ndc |
| rxcui | 1052760 | openfda.rxcui | |
| spl id | 2a807f1b-9870-a9ea-e063-6394a90aed25 | id | |
| spl set id | fb808dc5-bf80-836c-e053-6294a90a80aa | 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.