Home NDC 69842-602 Epsom Salt
Product NDC 69842-602
11-digit product format 698420602
Labeler code 69842
Product ID 69842-602_49ecf892-4ef3-9620-e063-6294a90a6e2b
Type HUMAN OTC DRUG
Nonproprietary name Magnesium Sulfate
Dosage form GRANULE, FOR SOLUTION
Route ORAL
Labeler CVS Pharmacy, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 1998-07-15
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 69842-602 69842-602-04 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 69842-602 69842-602-04 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 69842-602-04 Epsom Salt 2720 g in 1 POUCH GRANULE, FOR SOLUTION 2720 15 69842-602-07 Epsom Salt 1810 g in 1 POUCH GRANULE, FOR SOLUTION 1810 15 69842-602-80 Epsom Salt 3620 g in 1 POUCH GRANULE, FOR SOLUTION 3620 15
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-602 EPSOM SALT (MAGNESIUM SULFATE) GRANULE, FOR SOLUTION [CVS PHARMACY] 13 Current NDC, Legacy NDC, 3 package rows 20240808_a78d991a-ba21-4bc4-b8f9-f8dafbddc28f.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 69842-602-04 69842060204 2720 g in 1 POUCH (69842-602-04) 2720 g 1998-07-15 0000-00-00 No No Current 69842-602-07 69842060207 1810 g in 1 POUCH (69842-602-07) 1810 g 1998-07-15 0000-00-00 No No Current 69842-602-80 69842060280 3620 g in 1 POUCH (69842-602-80) 3620 g 1998-07-15 0000-00-00 No No Current