Home NDC 0121-1760 Mag-AL Liquid
Product NDC 0121-1760
11-digit product format 001211760
Labeler code 0121
Product ID 0121-1760_23f8e329-625d-1e98-e063-6394a90a7df2
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Hydroxide and Magnesium Hydroxide
Dosage form SUSPENSION
Route ORAL
Labeler PAI Holdings, LLC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-01-14
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE
Active strength 200; 200 mg/5mL; mg/5mL
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 Mag-AL Liquid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 200 mg/5mL MAGNESIUM HYDROXIDE 200 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup 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 243463 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 0121-1760-30 Mag-AL Liquid 10 in 1 CASE SUSPENSION 10 7 0121-1760-30 Mag-AL Liquid 10 in 1 TRAY SUSPENSION 10 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Aluminum Hydroxide ACTIVE INGREDIENT 5QB0T2IUN0 MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Magnesium Hydroxide ACTIVE INGREDIENT NBZ3QY004S MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Aluminum Hydroxide ACTIVE MOIETY 5QB0T2IUN0 MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Hydroxide Ion ACTIVE MOIETY 9159UV381P MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Butylparaben INACTIVE INGREDIENT 3QPI1U3FV8 MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Cyclomethicone 4 INACTIVE INGREDIENT CZ227117JE MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Hypromellose 2910 (4000 MPA.S) INACTIVE INGREDIENT RN3152OP35 MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Peppermint Oil INACTIVE INGREDIENT AV092KU4JH MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Propylparaben INACTIVE INGREDIENT Z8IX2SC1OH MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Saccharin Sodium INACTIVE INGREDIENT SB8ZUX40TY MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Sorbitol INACTIVE INGREDIENT 506T60A25R MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1 Water INACTIVE INGREDIENT 059QF0KO0R MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0121-1760 MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PAI HOLDINGS, LLC] 7 Current NDC, Legacy NDC, 2 package rows 20241010_b1f2d137-f5f7-4800-a1df-ef5d25544bc9.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 14 of 34 · 675 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Equate Ultra Stregth Antacid CALCIUM CARBONATE Wal-Mart Stores, Inc. cdfe5c95-3f90-4620-a618-18bac0471c3e 2025-12-03 Warnings Exact identifier application number: M001 Walgreens Fast Acting Heartburn Relief Extra Strength ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE WALGREEN CO. 6eae97f3-a174-4cbc-badc-777475d2f7af 2025-11-26 Warnings Exact identifier application number: M001 Antacid Regular Strength ANTACID WALGREEN CO. ce5eef7f-497d-4c88-be6a-17eeb6e07f5b 2025-11-25 Warnings Exact identifier application number: M001 Antacid Extra Strength ANTACID WALGREEN CO. 2981c5f7-121a-4030-86b1-559061030e7a 2025-11-25 Warnings Exact identifier application number: M001 Antacid Extra Strength ANTACID CALCIUM CARBONATE WALGREEN CO. 14baa410-6ce3-4ddb-aac7-e2172d1506c4 2025-11-25 Warnings Exact identifier application number: M001 Antacid Extra Strength ANTACID WALGREEN CO. aa797e94-6560-41c9-8c71-458a1086e841 2025-11-25 Warnings Exact identifier application number: M001 Extra Strength Antacid CALCIUM CARBONATE WALGREEN COMPANY d66ec376-9cac-4de5-aac8-7c6f9aa210ce 2025-11-25 Warnings Exact identifier application number: M001 Antacid Extra Strength Wintergreen ANTACID WALGREEN CO. ae2cd8fb-73e2-43f4-8aa9-f92b06e21a6d 2025-11-25 Warnings Exact identifier application number: M001 Antacid Ultra Strength ANTACID WALGREEN CO. 09ef90c3-1fc3-48be-8071-2fa387a46175 2025-11-25 Warnings Exact identifier application number: M001 Antacid Ultra Strength Assorted Fruits ANTACID WALGREEN CO. 6d6cecdc-646b-4c7b-b325-9423c29c57fc 2025-11-25 Warnings Exact identifier application number: M001 Antacid Ultra Strength Assorted Fruits ANTACID WALGREEN CO. e1b55f3a-c6d7-4374-acc7-134786a3765e 2025-11-25 Warnings Exact identifier application number: M001 ULTRA STRENGTH Antacid CALCIUM CARBONATE WALGREEN CO a4dcf7b9-d2c3-45d3-9410-fc4d55052a3c 2025-11-25 Warnings Exact identifier application number: M001 FAST ACTING Heartburn Relief ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE WALGREEN CO. 48c14005-811a-4868-b33e-934845504856 2025-11-25 Warnings Exact identifier application number: M001 Walgreens Childrens Saline Laxative MAGNESIUM HYDROXIDE WALGREEN CO. 3813ed22-cf68-4c16-9b61-c39828120079 2025-11-25 Warnings Exact identifier application number: M001 Ultra Strength Assorted Berries CALCIUM CARBONATE SAM'S WEST INC bc619258-7451-460c-9472-95678ea82d6e 2025-11-20 Warnings Exact identifier application number: M001 Gelusil ALUMINA, MAGNESIA, SIMETHICONE WellSpring Pharmaceutical Corporation 92fbeec1-1562-40f3-9734-41f133d494f9 2025-11-20 Warnings Exact identifier application number: M001 GERI-MOX ANTACID ANTIGAS ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE Geri-Care Pharmaceuticals, Corp 03358bc7-8819-4a05-bc13-27fbf486bd26 2025-11-20 Warnings Exact identifier application number: M001 Melox ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE Belmora LLC d41f0b26-5add-4045-9754-37d70d120d28 2025-11-20 Warnings Exact identifier application number: M001 Tums Chewy Bites Vanilla and Mint CALCIUM CARBONATE Haleon US Holdings LLC 2b9dd909-c850-3c21-e063-6394a90a15a8 2025-11-19 Warnings Exact identifier application number: M001 MAXIMUM STRENGTH ANTACID ANTIGAS ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE WALGREEN COMPANY 7cd8fdf4-f762-f936-e053-2a91aa0aa6ee 2025-11-19 Warnings Exact identifier application number: M001
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 0121-1760-30 00121176030 10 TRAY in 1 CASE (0121-1760-30) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE 10 tray 2004-01-14 0000-00-00 No No Current