FDA.reportPublic FDA data

Magnesium Citrate

Product NDC
41520-329
Requested package NDC
41520-329-10
11-digit product format
415200329
Labeler code
41520
Product ID
41520-329_896dac44-c089-4db4-9573-0a0ef881aa0b
Type
HUMAN OTC DRUG
Nonproprietary name
Magnesium citrate
Dosage form
LIQUID
Route
ORAL
Labeler
Care One (American Sales Company)
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-05-31
Marketing end
2023-12-29
Substance
MAGNESIUM CITRATE
Active strength
2 g/29.6mL
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 packagepackage41520-32941520-329-10DDiscontinued by firm2026-10-05

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 · 12 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…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MAGNESIUM CITRATEACTIVE INGREDIENTRHO26O1T9VMAGNESIUM CITRATE LIQUID [CARE ONE (AMERICAN SALES COMPANY)]1
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY838MAGNESIUM CITRATE LIQUID [CARE ONE (AMERICAN SALES COMPANY)]1
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLMAGNESIUM CITRATE LIQUID [CARE ONE (AMERICAN SALES COMPANY)]1
SACCHARIN SODIUM ANHYDROUSINACTIVE INGREDIENTI4807BK602MAGNESIUM CITRATE LIQUID [CARE ONE (AMERICAN SALES COMPANY)]1
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOMAGNESIUM CITRATE LIQUID [CARE ONE (AMERICAN SALES COMPANY)]1
WATERINACTIVE INGREDIENT059QF0KO0RMAGNESIUM CITRATE LIQUID [CARE ONE (AMERICAN SALES COMPANY)]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41520-329-1041520032910296 mL in 1 BOTTLE, GLASS (41520-329-10) 296 ml2015-05-312023-12-29NoNoCurrent