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 25 of 34 · 675 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Calcium Carbonate 1250 mg CALCIUM CARBONATE CitraGen Pharmaceuticals, Inc. 766b3f3f-8bd1-281c-e053-2991aa0af54b 2025-01-30 Warnings Exact identifier application number: M001 Calcium Carbonate 10 gr (648 mg) CALCIUM CARBONATE CitraGen Pharmaceuticals, Inc. 723b940d-4f4b-f2e6-e053-2991aa0a8bcc 2025-01-30 Warnings Exact identifier application number: M001 Ultra Strength Antacid CALCIUM CARBONATE CVS 2bc4c71c-a9c5-17df-e063-6294a90ac88c 2025-01-27 Warnings Exact identifier application number: M001 Goodsense Ultra Strength Antacid CALCIUM CARBONATE Good Sense (Geiss, Destin & Dunn, Inc.) 492deace-7ea1-4fe3-a4c7-b2c6f195d68c 2025-01-20 Warnings Exact identifier application number: M001 Calcium Carbonate 10 gr (648 mg) (Antacid) CALCIUM CARBONATE 10GR (648 MG) Ulai Health LLC 641ae5b9-3bb6-41a1-ab12-367bf2fbcb0a 2025-01-20 Warnings Exact identifier application number: M001 GoodSense Extra Strength Antacid CALCIUM CARBONATE GoodSense 2fcdeb06-17de-49d8-97bb-8d31e1c0c61f 2025-01-20 Warnings Exact identifier application number: M001 HEB Extra Stregth Antacid CALCIUM CARBONATE H E B dcfe4c81-b6e0-4a9b-a521-f3ad0c0a8e48 2025-01-20 Warnings Exact identifier application number: M001 Aluminum Hydroxide, Magnesium Hydroxide and Simethicone ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE Everpharm LLC 2bda74cb-e77d-46bb-e063-6394a90af580 2025-01-16 Warnings Exact identifier application number: M001 Childrens Antacid CALCIUM CARBONATE CVS 1bf90c0c-b639-1c06-e063-6394a90ab85b 2025-01-16 Warnings Exact identifier application number: M001 Sodium Bicarbonate SODIUM BICARBONATE World Perfumes Inc a83544e4-ec09-1e95-e053-2995a90ab7b9 2025-01-15 Warnings Exact identifier application number: M001 Sodium Bicarbonate 10 gr SODIUM BICARBONATE Reliable 1 Laboratories LLC 321a772c-c44c-3d4e-e054-00144ff8d46c 2025-01-15 Warnings Exact identifier application number: M001 Calcium Carbonate 500 mg CALCIUM CARBONATE Reliable 1 Laboratories LLC 322f1b54-abe9-11a7-e054-00144ff8d46c 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a27a71-b7b2-12aa-e063-6294a90a312f 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a7720f-1e74-7578-e063-6394a90a5eae 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a78060-7f0d-c4bd-e063-6294a90ae152 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a78a5c-e3b5-f362-e063-6394a90a0807 2025-01-15 Warnings Exact identifier application number: M001 Rolaids Extra Strength Mint CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE Chattem, Inc. 604d79f3-cdfa-45e2-8c20-fa6e0ff09b2e 2025-01-15 Warnings Exact identifier application number: M001 Extra Strength Smooth Antacid CALCIUM CARBONATE H E B 19a3221f-e0c1-c47a-e063-6394a90a1f01 2025-01-14 Warnings Exact identifier application number: M001 Childrens Stomach Relief Antacid CALCIUM CARBONATE H E B 18fae1aa-1001-8035-e063-6394a90adc66 2025-01-14 Warnings Exact identifier application number: M001 Calcium Carbonate 10 gr (648 mg) (Antacid) CALCIUM CARBONATE 10GR (648 MG) Aphena Pharma Solutions - Tennessee, LLC ac839363-94fd-4c60-b5b6-70e4488ce1dd 2025-01-09 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