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 (canonical bytes are SHA-256 checked before publication)

Brand name: Magnesium Citrate
Generic name: MAGNESIUM CITRATE ORAL SOLUTION
Manufacturer: Bionpharma, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4019fbd0-fcf9-77a6-e063-6294a90a5ae7
SPL ID: 4019f5bb-f9df-92fc-e063-6394a90aa042
Version: 1
Effective date: 2025-09-30
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:46

Harmonized routes table
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.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Magnesium Citrate	openfda.brand_name
generic name		MAGNESIUM CITRATE ORAL SOLUTION	openfda.generic_name
manufacturer name		Bionpharma, Inc.	openfda.manufacturer_name
ndc	package	69452-398-98	openfda.package_ndc
ndc	product	69452-398	openfda.product_ndc
ndc11	package	69452039898	derived:openfda.package_ndc
rxcui		1052760	openfda.rxcui
spl id		4019f5bb-f9df-92fc-e063-6394a90aa042	id
spl set id		4019fbd0-fcf9-77a6-e063-6294a90a5ae7	set_id
unii		RHO26O1T9V	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor before use if you have ■ Kidney disease ■ a magnesium restricted diet ■ Abdominal 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

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.