Magnesium Citrate

Product NDC
55319-029
Requested package NDC
55319-029-10
11-digit product format
553190029
Labeler code
55319
Product ID
55319-029_869ffa92-3784-4897-8519-d3617c2ade6b
Type
HUMAN OTC DRUG
Nonproprietary name
Magnesium citrate
Dosage form
LIQUID
Route
ORAL
Labeler
Family Dollar (FAMILY WELLNESS)
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-05-31
Marketing end
2025-05-30
Substance
MAGNESIUM CITRATE
Active strength
2 g/29.6mL
Pharmacologic classes
Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage55319-02955319-029-10DDiscontinued by firm2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 5 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2022-08-30 03:57 UTC · source 2022-08-29IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55319-029-102022-10-31C16284748780-1d6a99b39-6aed-a426-e053-dadaa90af4c2Drug Facts
55319-029-102022-01-28C16284748780-1d6a99b39-6aed-a426-e053-dadaa90af4c2Drug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MAGNESIUM CITRATEACTIVE INGREDIENTRHO26O1T9VMAGNESIUM CITRATE LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]1
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY838MAGNESIUM CITRATE LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]1
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLMAGNESIUM CITRATE LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYMAGNESIUM CITRATE LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]1
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOMAGNESIUM CITRATE LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]1
WATERINACTIVE INGREDIENT059QF0KO0RMAGNESIUM CITRATE LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55319-029MAGNESIUM CITRATE LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]5Legacy NDC20221101_9ac36fa1-17c2-44de-ba74-33d3a652a4cd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55319-029-1055319002910296 mL in 1 BOTTLE, GLASS (55319-029-10) 296 ml2015-05-312025-05-30NoNoCurrent