Home NDC 15631-2833 MAGNESIA PHOS
Product NDC 15631-2833
11-digit product format 156312833
Labeler code 15631
Product ID 15631-2833_19cf3431-37ee-dcf8-e063-6394a90ae7d3
Type HUMAN OTC DRUG
Nonproprietary name MAGNESIA PHOS
Dosage form LIQUID
Route ORAL
Labeler Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-05-23
Substance MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength 1 [hp_X]/mL
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 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 MAGNESIA PHOS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 1 [hp_X]/mL
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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 15631-2833-0 MAGNESIA PHOS 10 mL in 1 BOTTLE LIQUID 10 1 15631-2833-1 MAGNESIA PHOS 30 mL in 1 BOTTLE LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 15631-2833 MAGNESIA PHOS LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC] 1 Current NDC, 2 package rows 20240612_19cf2bbd-0f15-78a7-e063-6394a90a1647.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 Sample Exclude flag Status 15631-2833-0 15631283300 10 mL in 1 BOTTLE (15631-2833-0) 10 ml 2024-05-23 No No Current 15631-2833-1 15631283301 30 mL in 1 BOTTLE (15631-2833-1) 30 ml 2024-05-23 No No Current