Home NDC 41250-602 Epsom Salt
Product NDC 41250-602
11-digit product format 412500602
Labeler code 41250
Product ID 41250-602_4b340dae-832a-9be5-e063-6394a90a13b8
Type HUMAN OTC DRUG
Nonproprietary name Magnesium Sulfate
Dosage form GRANULE, FOR SOLUTION
Route ORAL; TOPICAL
Labeler Meijer, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-04-26
Substance MAGNESIUM SULFATE HEPTAHYDRATE
Active strength 1 g/g
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 2027-12-31
Current FDA listing Yes 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Epsom Salt
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM SULFATE HEPTAHYDRATE 1 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SK47B8698T Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1053346 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-602-07 Epsom Salt 1814 g in 1 POUCH GRANULE, FOR SOLUTION 1814 17 41250-602-43 Epsom Salt 454 g in 1 POUCH GRANULE, FOR SOLUTION 454 17 41250-602-80 Epsom Salt 3628 g in 1 POUCH GRANULE, FOR SOLUTION 3628 17
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-602 EPSOM SALT (MAGNESIUM SULFATE) GRANULE, FOR SOLUTION [MEIJER DISTRIBUTION, INC] 14 Current NDC, Legacy NDC, 3 package rows 20241202_2070a4a6-7968-49f2-84ec-53bd1cd82445.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 14 of 42 · 833 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 41250-602-07 41250060207 1814 g in 1 POUCH (41250-602-07) 1814 g 2013-04-26 0000-00-00 No No Current 41250-602-43 41250060243 454 g in 1 POUCH (41250-602-43) 454 g 2013-04-26 0000-00-00 No No Current 41250-602-80 41250060280 3629 g in 1 POUCH (41250-602-80) 3629 g 2013-04-26 0000-00-00 No No Current