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

Additional Listing Data#

Finished product
Yes
Brand name base
Mag-AL Liquid
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALUMINUM HYDROXIDE200 mg/5mL
MAGNESIUM HYDROXIDE200 mg/5mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5QB0T2IUN0, NBZ3QY004S
Rxcui243463

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0121-1760-30Mag-AL Liquid10 in 1 CASESUSPENSION107
0121-1760-30Mag-AL Liquid10 in 1 TRAYSUSPENSION107

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0121-1760-30ML - Milliliter0121-1760a959079c-4307-4f87-abd6-eb39a2359c8b12014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Aluminum HydroxideACTIVE INGREDIENT5QB0T2IUN0MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Magnesium HydroxideACTIVE INGREDIENTNBZ3QY004SMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Aluminum HydroxideACTIVE MOIETY5QB0T2IUN0MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Hydroxide IonACTIVE MOIETY9159UV381PMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
ButylparabenINACTIVE INGREDIENT3QPI1U3FV8MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Cyclomethicone 4INACTIVE INGREDIENTCZ227117JEMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Hypromellose 2910 (4000 MPA.S)INACTIVE INGREDIENTRN3152OP35MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Peppermint OilINACTIVE INGREDIENTAV092KU4JHMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
PropylparabenINACTIVE INGREDIENTZ8IX2SC1OHMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
Saccharin SodiumINACTIVE INGREDIENTSB8ZUX40TYMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
SorbitolINACTIVE INGREDIENT506T60A25RMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RMAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PHARMACEUTICAL ASSOCIATES, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0121-1760MAG-AL LIQUID (ALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDE) SUSPENSION [PAI HOLDINGS, LLC]7Current NDC, Legacy NDC, 2 package rows20241010_b1f2d137-f5f7-4800-a1df-ef5d25544bc9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
243463aluminum hydroxide 200 MG / magnesium hydroxide 200 MG in 5 mL Oral SuspensionPSNb1f2d137-f5f7-4800-a1df-ef5d25544bc97
243463aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML Oral SuspensionSCDb1f2d137-f5f7-4800-a1df-ef5d25544bc97
243463aluminum hydroxide 1200 MG / magnesium hydroxide 1200 MG per 30 ML Oral SuspensionSYb1f2d137-f5f7-4800-a1df-ef5d25544bc97
243463aluminum hydroxide 200 MG / milk of magnesia 200 MG per 5 ML Oral SuspensionSYb1f2d137-f5f7-4800-a1df-ef5d25544bc97

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0121-1760-300012117603010 TRAY in 1 CASE (0121-1760-30) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE10 tray2004-01-140000-00-00NoNoCurrent