Mag-al Liquid by A-S Medication Solutions Mag-al Liquid

Mag-al Liquid by

Drug Labeling and Warnings

Mag-al Liquid by is a Otc medication manufactured, distributed, or labeled by A-S Medication Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MAG-AL LIQUID- aluminum hydroxide and magnesium hydroxide suspension 
A-S Medication Solutions

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 mg	Antacid
Magnesium hydroxide 200 mg	Antacid

Uses

for the relief of:

• acid indigestion
• heartburn
• sour stomach
• upset stomach due to these symptoms

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

• shake well before using
• do not take more than 16 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 weeks

• adults and children 12 years and older: take 2 to 4 teaspoonfuls four times a day or as directed by a physician
• children under 12 years: consult a physician

Other information

• each 5 mL contains: magnesium 83 mg, sodium 1.34 mg
• does not meet USP requirements for preservative effectiveness
• store at controlled room temperature 20° - 25°C (68° - 77°F)
• protect from freezing
• White colored, peppermint flavored liquid supplied in the following oral dosage form:

• NDC: 0121-1760-30: 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

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

R05/19

HOW SUPPLIED

Product: 50090-2802

Storage

store at controlled room temperature 20° - 25°C (68° - 77°F) protect from freezing

Aluminum Hydroxide and Magnesium Hydroxide

MAG-AL LIQUID 
aluminum hydroxide and magnesium hydroxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50090-2802(NDC: 0121-1760)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)	ALUMINUM HYDROXIDE	200 mg  in 5 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P)	MAGNESIUM HYDROXIDE	200 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color	white	Score
Shape		Size
Flavor	PEPPERMINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50090-2802-0	10 in 1 CASE	01/20/2017	02/28/2019
1		10 mL in 1 TRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	01/14/2004	02/28/2019

Labeler - A-S Medication Solutions (830016429)

Establishment
Name	Address	ID/FEI	Business Operations
A-S Medication Solutions		830016429	RELABEL(50090-2802)

Revised: 1/2020

Document Id: 2ecdc08e-b806-46bd-9120-a0eb6050b8a5

34390-5

Set id: 5fe0fe0b-db08-40a4-9bbf-90b919374320

Version: 5

Effective Time: 20200118

 

A-S Medication Solutions