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
- HARRIS TEETER MAGNESIUM CITRATE ORAL SOLUTION - LEMON
- Manufacturer
- Harris Teeter, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1e8e01fc-2c89-9722-e063-6394a90a6acf
- SPL ID
- 1e93fea9-7ab7-c2b7-e063-6294a90a75b5
- Version
- 2
- Effective date
- 2024-07-31
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:36:01
| 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 | HARRIS TEETER MAGNESIUM CITRATE ORAL SOLUTION - LEMON | openfda.generic_name | |
| manufacturer name | Harris Teeter, LLC | openfda.manufacturer_name | |
| ndc | package | 69256-311-10 | openfda.package_ndc |
| ndc | product | 69256-311 | openfda.product_ndc |
| ndc11 | package | 69256031110 | derived:openfda.package_ndc |
| rxcui | 1052760 | openfda.rxcui | |
| spl id | 1e93fea9-7ab7-c2b7-e063-6294a90a75b5 | id | |
| spl set id | 1e8e01fc-2c89-9722-e063-6394a90a6acf | 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.