Home NDC 56062-649 MILK OF MAGNESIA
Product NDC 56062-649
11-digit product format 560620649
Labeler code 56062
Product ID 56062-649_09a6ec32-81af-6da6-e063-6294a90abb46
Type HUMAN OTC DRUG
Nonproprietary name magnesium hydroxide
Dosage form SUSPENSION
Route ORAL
Labeler Publix
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-08-01
Substance MAGNESIUM HYDROXIDE
Active strength 1200 mg/15mL
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 MILK OF MAGNESIA
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM HYDROXIDE 1200 mg/15mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination NBZ3QY004S Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 253017 Internal RxNorm 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 56062-649-12 MILK OF MAGNESIA 355 mL in 1 BOTTLE SUSPENSION 355 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56062-649 MILK OF MAGNESIA (MAGNESIUM HYDROXIDE) SUSPENSION [PUBLIX] 3 Current NDC, Legacy NDC, 1 package rows 20231109_cbf7dcef-7623-b333-e053-2a95a90a0f1a.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 17 of 42 · 833 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 56062-649-12 56062064912 355 mL in 1 BOTTLE (56062-649-12) 355 ml 2021-08-01 0000-00-00 No No Current