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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
b1f2d137-f5f7-4800-a1df-ef5d25544bc9	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6e3c022f-0786-43f1-8857-edff89d5153f	Product name	1	20260309
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
efd58652-cb8f-4018-91ca-4b0eb2ff729f	Product name	7	20240226
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62	Product name	3	20210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
e7e58cd3-cacb-49df-8d34-1ee335614abb	Product name	1	20150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0121-1760-30	ML - Milliliter	0121-1760	a959079c-4307-4f87-abd6-eb39a2359c8b	1	2014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
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 31 of 34 · 667 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tums Chewy Bites Mixed Fruit	CALCIUM CARBONATE	Haleon US Holdings LLC	d341b832-edcf-4cb2-96e1-c303b030c59a	2024-03-02	Warnings	Exact identifier application number: M001
Tums Chewy Bites	CALCIUM CARBONATE	Haleon US Holdings LLC	5090f60f-fa98-470b-bafd-bb64e6b28fcc	2024-03-02	Warnings	Exact identifier application number: M001
Tums Chewy Bites	CALCIUM CARBONATE	Haleon US Holdings LLC	453ceee1-414b-4f4c-8408-eb540a79ca05	2024-03-02	Warnings	Exact identifier application number: M001
Tums Chewy Bites Berry Shake	CALCIUM CARBONATE	Haleon US Holdings LLC	9043983c-7ee4-4971-8885-36f814bb570f	2024-03-02	Warnings	Exact identifier application number: M001
Tums Chewy Delights	CALCIUM CARBONATE	Haleon US Holdings LLC	189850d0-6f06-45bd-bd7e-9063ee580d0b	2024-03-02	Warnings	Exact identifier application number: M001
Sodium Bicarbonate	SODIUM BICARBONATE	Bryant Ranch Prepack	4493d7c5-f2c3-416e-a5c1-35398fc7f61d	2024-02-29	Boxed warning, Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID AND ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	STRATEGIC SOURCING SERVICES LLC	fe04c244-d9b8-2800-e053-6294a90aeedc	2024-02-06	Warnings	Exact identifier application number: M001
Mylanta Classic	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE	Infirst Healthcare Inc.	10a4cf29-39ed-87c3-e063-6394a90a4973	2024-02-05	Warnings	Exact identifier application number: M001
Mylanta Vanilla Caramel	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE	Infirst Healthcare Inc.	10a66d74-74b4-3f8d-e063-6394a90a7f00	2024-02-05	Warnings	Exact identifier application number: M001
Mylanta Maximum Strength Vanilla Caramel Flavor	ANTACID AND ANTI GAS ALUMINUM HYDROXIDE MAGNESIUM HYDROXIDE AND SIMETHICONE	Infirst Healthcare Inc.	ace5cae4-3a78-41c3-987d-59ce22dca2ac	2024-01-01	Warnings	Exact identifier application number: M001
Mylanta Coat and Cool	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE	INFIRST HEALTHCARE INC.	b6571f7f-e1ea-4034-a46c-4de1d01beec3	2024-01-01	Warnings	Exact identifier application number: M001
Sodium Bicarbonate	SODIUM BICARBONATE	Pharma Nobis, LLC	e42f674b-1a70-6a3c-e053-2995a90afa72	2023-12-22	Warnings	Exact identifier application number: M001
Premier Value Milk of Magnesia	MAGNESIUM HYDROXIDE	Pharmacy Value Alliance, LLC	c3cdaa2b-db34-872d-e053-2995a90a3826	2023-12-20	Warnings	Exact identifier application number: M001
Calcium Carbonate	CALCIUM CARBONATE	Humco Holding Group, Inc.	8b207b49-d3fd-4108-b611-dca27c9dc78a	2023-12-15	Warnings	Exact identifier application number: M001
Humco Dewees Carminative	MAGNESIUM CARBONATE	Humco Holding Group, inc.	163bceeb-ca74-413e-88b9-5c7bc9bbeb0d	2023-12-15	Warnings	Exact identifier application number: M001
Humco Milk of Magnesia	MAGNESIUM HYDROXIDE	Humco Holding Group, Inc.	b6c90fb4-2673-7e29-e053-2995a90ae9e1	2023-12-15	Warnings	Exact identifier application number: M001
Medis Sodium Bicarbonate	SODIUM BICARBONATE	Humco Holding Group, Inc	5da32469-58fc-14b1-e053-2a91aa0a74c4	2023-12-15	Warnings	Exact identifier application number: M001
Mylanta One Antacid/Anti-Gas	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, DIMETHICONE	Infirst Healthcare Inc.	aa694e0d-7891-4870-8106-dd57f1e29fb4	2023-12-11	Warnings	Exact identifier application number: M001
Mylanta One Antacid/Anti-Gas	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, DIMETHICONE	Infirst Healthcare Inc.	ed1b03f0-fabc-4c1c-8e6d-9f15c380300c	2023-12-11	Warnings	Exact identifier application number: M001
Inon Ace	MAGNESIUM ALUMINOSILICATE, MAGNESIUM HYDROXIDE	Sato Pharmaceutical Co., Ltd.	a6e4475c-dfac-493c-b98a-21473e3b59d5	2023-12-06	Warnings	Exact identifier application number: M001

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5QB0T2IUN0	ALUMINUM HYDROXIDE	21645-51-2	ALUMINUM HYDROXIDE
NBZ3QY004S	MAGNESIUM HYDROXIDE	1309-42-8	MAGNESIUM HYDROXIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
243463	aluminum hydroxide 200 MG / magnesium hydroxide 200 MG in 5 mL Oral Suspension	PSN	b1f2d137-f5f7-4800-a1df-ef5d25544bc9	7
243463	aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML Oral Suspension	SCD	b1f2d137-f5f7-4800-a1df-ef5d25544bc9	7
243463	aluminum hydroxide 1200 MG / magnesium hydroxide 1200 MG per 30 ML Oral Suspension	SY	b1f2d137-f5f7-4800-a1df-ef5d25544bc9	7
243463	aluminum hydroxide 200 MG / milk of magnesia 200 MG per 5 ML Oral Suspension	SY	b1f2d137-f5f7-4800-a1df-ef5d25544bc9	7

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Mag-AL Liquid	PAI Holdings, LLC \| PAI Holdings, LLC dba Pharmaceutical Associates, Inc.	2024-10-08	HUMAN OTC DRUG LABEL	7
Mag-al Liquid	A-S Medication Solutions	2021-03-01	HUMAN OTC DRUG LABEL	6