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

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Mag-AL Plus

Drug Facts

Active ingredients (in each 5 mL = 1 teaspoonful)Purpose
Aluminum hydroxide (equiv. to dried gel, USP) 200 mgAntacid
Magnesium hydroxide 200 mgAntacid
Simethicone 20 mgAntigas

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 0121-1761-30:30 mL unit dose cup. Case contains 100 unit dose cups of 30 mL packaged in 10 trays of 10 unit dose cups each.

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

PRINCIPAL DISPLAY PANEL - 30 mL Unit-Dose Cup Tray Label

Delivers 30 mL

NDC 0121-1761-30

MAG-AL PLUS

Each 30 mL contains:

Aluminum Hydroxide  1200 mg

Magnesium Hydroxide  1200 mg

Simethicone  120 mg

SHAKE WELL

USUAL DOSAGE: See attached Drug Facts

Package Not Child-Resistant

Pharmaceutical Associates, Inc.
Greenville, SC 29605

SEE INSERT

PRINCIPAL DISPLAY PANEL - 30 mL Unit-Dose Cup Tray Label
MAG-AL PLUS 
aluminum hydroxide, magnesium hydroxide, and simethicone suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0121-1761
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
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE20 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)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0121-1761-3010 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 DrugM00101/14/2004
Labeler - PAI Holdings, LLC (044940096)
Establishment
NameAddressID/FEIBusiness Operations
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma097630693manufacture(0121-1761)

Revised: 12/2022
Document Id: 0ea0464a-35c2-48c9-88c0-d598cbd887c3
Set id: 896ab07a-1b40-43ab-8589-3be86b1c4198
Version: 8
Effective Time: 20221222
 
PAI Holdings, LLC