FDA.reportPublic FDA data

Magnesium Citrate

Product NDC
49035-329
Requested package NDC
49035-329-10
11-digit product format
490350329
Labeler code
49035
Product ID
49035-329_07603772-adc9-4dca-9be4-1b15a3b6de08
Type
HUMAN OTC DRUG
Nonproprietary name
Magnesium citrate
Dosage form
LIQUID
Route
ORAL
Labeler
EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-10-31
Marketing end
2025-01-31
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 packagepackage49035-32949035-329-10DDiscontinued 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 · 6 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-329-10ML - Milliliter49035-32983004a42-66a9-47d5-b896-82e589bc1cba12017-08-11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MAGNESIUM CITRATEACTIVE INGREDIENTRHO26O1T9VMAGNESIUM CITRATE LIQUID [EQUATE (WALMART STORES, INC.)]2
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY838MAGNESIUM CITRATE LIQUID [EQUATE (WALMART STORES, INC.)]2
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLMAGNESIUM CITRATE LIQUID [EQUATE (WALMART STORES, INC.)]2
SACCHARIN SODIUM ANHYDROUSINACTIVE INGREDIENTI4807BK602MAGNESIUM CITRATE LIQUID [EQUATE (WALMART STORES, INC.)]2
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOMAGNESIUM CITRATE LIQUID [EQUATE (WALMART STORES, INC.)]2
WATERINACTIVE INGREDIENT059QF0KO0RMAGNESIUM CITRATE LIQUID [EQUATE (WALMART STORES, INC.)]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-329-1049035032910296 mL in 1 BOTTLE, GLASS (49035-329-10) 296 ml2014-10-312025-01-31NoNoCurrent