Home NDC 79903-324 Gentle Laxative
Product NDC 79903-324
11-digit product format 799030324
Labeler code 79903
Product ID 79903-324_2d7f73ed-465b-b658-e063-6394a90ae525
Type HUMAN OTC DRUG
Nonproprietary name magnesium hydroxide
Dosage form LIQUID
Route ORAL
Labeler WALMART INC.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-01
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 Gentle Laxative
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 79903-324-12 Gentle Laxative 355 mL in 1 BOTTLE LIQUID 355 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-324 GENTLE LAXATIVE (MAGNESIUM HYDROXIDE) LIQUID [WALMART INC.] 2 Current NDC, 1 package rows 20250209_26b9f247-c242-2925-e063-6394a90a68dd.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 Sample Exclude flag Status 79903-324-12 79903032412 355 mL in 1 BOTTLE (79903-324-12) 355 ml 2025-02-01 No No Current