Home NDC 0220-3236 Magnesia phosphorica
Product NDC 0220-3236
11-digit product format 002203236
Labeler code 0220
Product ID 0220-3236_00edfde0-0394-2226-e063-6294a90af199
Type HUMAN OTC DRUG
Nonproprietary name MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength 12 [hp_X]/12[hp_X]
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 phosphorica
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/12[hp_X]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination HF539G9L3Q 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 0220-3236-41 Magnesia phosphorica 12 [hp_X] in 1 TUBE PELLET 12 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-3236 MAGNESIA PHOSPHORICA (MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230721_86305481-9dd1-94b2-e053-2a91aa0a5ad4.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 0220-3236-41 00220323641 12 [hp_X] in 1 TUBE (0220-3236-41) 1983-03-03 0000-00-00 No No Current