Home NDC 37662-1035 Magnesia Sulphurica
Product NDC 37662-1035
11-digit product format 376621035
Labeler code 37662
Product ID 37662-1035_e46cb756-bb04-4a99-e053-2a95a90a3fd5
Type HUMAN OTC DRUG
Nonproprietary name Magnesia Sulphurica
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-07-22
Substance MAGNESIUM SULFATE HEPTAHYDRATE
Active strength 1 [hp_M]/1
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 1 [hp_M]/1
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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37662-1035-1 Magnesia Sulphurica 200 in 1 VIAL, GLASS PELLET 200 1 37662-1035-2 Magnesia Sulphurica 500 in 1 VIAL, GLASS PELLET 500 1 37662-1035-3 Magnesia Sulphurica 3000 in 1 BOTTLE, GLASS PELLET 3000 1 37662-1035-4 Magnesia Sulphurica 10000 in 1 BOTTLE, GLASS PELLET 10000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37662-1035 MAGNESIA SULPHURICA PELLET [HAHNEMANN LABORATORIES, INC.] 1 Current NDC, Legacy NDC, 4 package rows 20220724_e46cb756-bb03-4a99-e053-2a95a90a3fd5.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 Units Marketing start Marketing end Sample Exclude flag Status 37662-1035-1 37662103501 200 PELLET in 1 VIAL, GLASS (37662-1035-1) 200 pellet 2022-07-22 0000-00-00 No No Current 37662-1035-2 37662103502 500 PELLET in 1 VIAL, GLASS (37662-1035-2) 500 pellet 2022-07-22 0000-00-00 No No Current 37662-1035-3 37662103503 3000 PELLET in 1 BOTTLE, GLASS (37662-1035-3) 3000 pellet 2022-07-22 0000-00-00 No No Current 37662-1035-4 37662103504 10000 PELLET in 1 BOTTLE, GLASS (37662-1035-4) 10000 pellet 2022-07-22 0000-00-00 No No Current