Home NDC 68016-732 Epsom Salt
Product NDC 68016-732
11-digit product format 680160732
Labeler code 68016
Product ID 68016-732_5d9a7894-cc5b-42bd-aed4-f5eb226abf42
Type HUMAN OTC DRUG
Nonproprietary name Magnesium sulfate
Dosage form GRANULE
Route ORAL; TOPICAL
Labeler Chain Drug Consortium, LLC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-08-31
Marketing end 2026-12-31
Substance MAGNESIUM SULFATE, UNSPECIFIED
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
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 · 12 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 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM SULFATE, UNSPECIFIED 1 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination DE08037SAB 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# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68016-732-01 Epsom Salt 454 g in 1 POUCH GRANULE 454 10 68016-732-04 Epsom Salt 1814 g in 1 POUCH GRANULE 1814 10 68016-732-06 Epsom Salt 2720 g in 1 POUCH GRANULE 2720 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68016-732 EPSOM SALT (MAGNESIUM SULFATE) GRANULE [CHAIN DRUG CONSORTIUM, LLC] 9 Current NDC, Legacy NDC, 3 package rows 20250206_c9807e6e-9dcc-41a2-8956-b61623ac2176.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 68016-732-01 68016073201 454 g in 1 POUCH (68016-732-01) 454 g 2017-08-31 2026-12-31 No No Current 68016-732-04 68016073204 1814 g in 1 POUCH (68016-732-04) 1814 g 2017-08-31 2026-12-31 No No Current 68016-732-06 68016073206 2720 g in 1 POUCH (68016-732-06) 2720 g 2017-08-31 2026-12-31 No No Current