Mi-Acid Double Strength Antacid Tablets

Mi Acid by

Drug Labeling and Warnings

Mi Acid by is a Otc medication manufactured, distributed, or labeled by Major Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MI ACID- calcium carbonate, magnesium hydroxide tablet, chewable 
Major Pharmaceuticals

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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Mi-Acid Double Strength Antacid Tablets

Active ingredients (in each tablet)

Calcium carbonate 700 mg

Magnesium hydroxide 300 mg

Purpose

Antacid

Antacid

Uses

• relieves:
• acid indigestion
• heartburn
• sour stomach
• upset stomach associated with these symptoms

Enter section text here

Warnings

Ask a doctor before use if you have

• kidney disease
• a magnesium-restricted diet
  

Ask a doctor or pharmacist before use if

you are

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

Do not take more than 8 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

Keep out of reach of children. In case of overdose get a medical help or contact a Poison Control Center immediately.

• chew 2 to 4 tablets thoroughly as needed between meals and at bedtime or as directed by a doctor.
  

Other information

• each tablet contains: calcium 280 mg and magnesium 125 mg
• do not use if printed seal under cap is torn or missing.
• store at room temperature
• keep tightly closed and dry
  

corn starch, D&C yellow no. 10 lake, FD&C blue no. 1 lake, flavor, magnesium stearate, maltodextrin, sorbitol, sugar

PDP

Mi-AcidTM

Double Strength Antacid Tablets

Calcium Rich Antacid

Cool Mint Flavor

70 Chewable Tablets

Compare to the Active ingredients in Mylanta® Double Strength

MI ACID 
calcium carbonate, magnesium hydroxide tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0904-5115
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	700 mg
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P)	MAGNESIUM HYDROXIDE	300 mg

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SORBITOL (UNII: 506T60A25R)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	green	Score	no score
Shape	ROUND	Size	16mm
Flavor	MINT (Cool Mint)	Imprint Code	GDC111
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0904-5115-71	70 in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2003	12/19/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	01/03/2003	12/19/2019

Labeler - Major Pharmaceuticals (191427277)

Revised: 12/2019

Document Id: 4427dd06-2215-414f-9bd1-dd2557d5e539

34390-5

Set id: 71b7f8d6-9642-4696-9d7a-84fc8668423e

Version: 3

Effective Time: 20191219