MAG-AL PLUS XS- aluminum hydroxide, magnesium hydroxide, and dimethicone suspension 
PAI Holdings, LLC

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Mag-AL Plus XS

Drug Facts

Active ingredients (in each 5 mL = 1 teaspoonful)Purpose
Aluminum hydroxide (equiv. to dried gel, USP) 400 mgAntacid
Magnesium hydroxide 400 mgAntacid
Simethicone 40 mgAntigas

Uses for the relief of:

Warnings

Do not take more than 8 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 two times a day or as directed by a physician
children under 12 yearsconsult a physician

Other information

NDC 0121-1762-30: 30 mL unit dose cup. Case contains 100 unit dose cups of 30 mL packaged in 10 trays of 10 unit dose cups each.

*Maalox is a registered trademark of Novartis Consumer Health, Inc.

Inactive ingredients

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
www.paipharma.com

PRINCIPAL DISPLAY PANEL - 30 mL Cup Tray Label

Delivers 30 mL

NDC 0121-1762-30

MAG-AL PLUS XS

Each 30 mL contains:

Magnesium Hydroxide 2400 mg
Aluminum Hydroxide 2400 mg
Simethicone 240 mg

SHAKE WELL

Package Not Child-Resistant

Pharmaceutical Associates, Inc.
Greenville, SC 29605

See Insert

PRINCIPAL DISPLAY PANEL - 30 mL Cup Tray Label
MAG-AL PLUS  XS
aluminum hydroxide, magnesium hydroxide, and dimethicone suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0121-1762
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE400 mg  in 5 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE400 mg  in 5 mL
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE40 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
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0121-1762-3010 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 DrugM00201/14/2004
Labeler - PAI Holdings, LLC (044940096)
Establishment
NameAddressID/FEIBusiness Operations
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma097630693manufacture(0121-1762)

Revised: 8/2022
Document Id: 26a1e1ff-f122-4a93-bd12-038ba262677b
Set id: db0c47ab-5296-4195-9fa6-2e338b665094
Version: 7
Effective Time: 20220809
 
PAI Holdings, LLC