MAG-AL LIQUID- aluminum hydroxide and magnesium hydroxide suspension 
PAI Holdings, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Mag-AL Liquid

Drug Facts

Active ingredients (in each 5 mL = 1 teaspoonful)Purpose
Aluminum hydroxide (equiv. to dried gel, USP) 200 mgAntacid
Magnesium hydroxide 200 mgAntacid

Uses

for the relief of:

Warnings

Do not take more than 16 teaspoonfuls in a 24-hour period or use the maximum dosage for more than 2 weeks except under the advice and supervision of a physician.

Ask a doctor before use if you have

  • kidney disease
  • a magnesium-restricted diet

Ask a doctor or pharmacist before use if you are

  • presently taking a prescription drug. Antacids may interact with certain prescription drugs.

Stop use and ask a doctor if

  • symptoms last more than 2 weeks.

Keep out of reach of children.

Directions

adults and children 12 years and oldertake 2 to 4 teaspoonfuls four times a day or as directed by a physician
children under 12 yearsconsult a physician

Other information

NDC 0121-1760-30:30 mL unit dose cup, in a tray of ten cups.

Inactive ingredients

Antifoam af emulsion, butylparaben, hydroxypropyl methylcellulose, flavoring, propylene glycol, propylparaben, purified water, sodium saccharin, and sorbitol solution.

Questions or comments?

Call 1-800-845-8210

MANUFACTURED BY

Pharmaceutical
Associates, Inc.

Greenville, SC 29605

R07/21

PRINCIPAL DISPLAY PANEL - 30 mL Dose Cup Tray Label

Delivers 30 ML

NDC 0121-1760-30

MAG-AL Liquid

Each 30 mL contains:

Magnesium Hydroxide 1200 mg

Aluminum Hydroxide 1200 mg

SHAKE WELL

Package Not Child-Resistant

PRINCIPAL DISPLAY PANEL - 30 mL Dose Cup Tray Label
MAG-AL LIQUID 
aluminum hydroxide and magnesium hydroxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0121-1760
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE200 mg  in 5 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE200 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SORBITOL (UNII: 506T60A25R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
CYCLOMETHICONE 4 (UNII: CZ227117JE)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0121-1760-3010 in 1 CASE01/14/2004
110 in 1 TRAY
130 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33101/14/2004
Labeler - PAI Holdings, LLC (044940096)
Establishment
NameAddressID/FEIBusiness Operations
PAI Holdings, LLC dba Pharmaceutical Associates, Inc.097630693manufacture(0121-1760)

Revised: 3/2023
Document Id: e499949c-ef7f-4dd3-927d-b069e0625e82
Set id: b1f2d137-f5f7-4800-a1df-ef5d25544bc9
Version: 6
Effective Time: 20230302
 
PAI Holdings, LLC