Home NDC 53645-1680 Magnesia Phos
Product NDC 53645-1680
11-digit product format 536451680
Labeler code 53645
Product ID 53645-1680_faa4d343-4b62-a977-e053-6394a90a5744
Type HUMAN OTC DRUG
Nonproprietary name Magnesia Phos
Dosage form GLOBULE
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2014-02-03
Substance MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength 30 [hp_X]/23g
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 Phos
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 30 [hp_X]/23g
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 53645-1680-2 Magnesia Phos 23 g in 1 BOTTLE GLOBULE 23 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53645-1680 MAGNESIA PHOS GLOBULE [TRUE BOTANICA, LLC] 5 Current NDC, Legacy NDC, 1 package rows 20230502_619581f7-5a49-eb4c-e053-2991aa0a87a4.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 53645-1680-2 53645168002 23 g in 1 BOTTLE (53645-1680-2) 23 g 2014-02-03 0000-00-00 No No Current