Home NDC 0220-3267 Magnesia sulphurica
Product NDC 0220-3267
11-digit product format 002203267
Labeler code 0220
Product ID 0220-3267_0a1f2eba-411b-82ae-e063-6394a90a4b27
Type HUMAN OTC DRUG
Nonproprietary name MAGNESIUM SULFATE HEPTAHYDRATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance MAGNESIUM SULFATE HEPTAHYDRATE
Active strength 30 [hp_C]/30[hp_C]
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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Magnesia sulphurica
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM SULFATE HEPTAHYDRATE 30 [hp_C]/30[hp_C]
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 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 0220-3267-41 Magnesia sulphurica 30 [hp_C] in 1 TUBE PELLET 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-3267 MAGNESIA SULPHURICA (MAGNESIUM SULFATE HEPTAHYDRATE) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20231115_7d77a15c-c9ef-7778-e053-2991aa0aa0b6.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0220-3267-41 00220326741 30 [hp_C] in 1 TUBE (0220-3267-41) 1983-03-03 0000-00-00 No No Current