MI-ACID GAS RELIEF- simethicone tablet, chewable

Mi-Acid Gas Relief by

Drug Labeling and Warnings

Mi-Acid Gas Relief by is a Otc medication manufactured, distributed, or labeled by ATLANTIC BIOLOGICALS CORP.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Simethicone 80 mg

Purpose

Antigas

KEEP OUT OF REACH OF CHILDREN

Uses

relieves:

• pressure
• bloating
• symptoms referred to as gas
  

Warnings

Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center immediately.

Directions

• chew 2 to 4 tablets thoroughly as needed after meals and at bedtime.
• do not exceed 6 tablets per day unless directed by a physician.
  

Other information

• do not use if inner seal is broken.
• store at room temperature
• avoid high humidity and excessive heat, above 400C (1040F)
  

Inactive ingredients

compressible sugar, dextrose, flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, sorbitol

Questions or comments?

Call (800) 616-2471

DISTRIBUTED BY:

ATLANTIC BIOLOGICALS CORP.

MIAMI, FL 33179

PDP

NDC: 17856-5068-2

Mi-Acid Gas Relief

Relieves Gas Pain, Pressure and Bloating

Simethicone 80 mg/Antiflatulent

100 Chewable Tablets

INGREDIENTS AND APPEARANCE

MI-ACID GAS RELIEF 
simethicone tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17856-5068(NDC:0904-5068)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	80 mg

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	13mm
Flavor	PEPPERMINT	Imprint Code	GDC103
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17856-5068-2	1 in 1 POUCH; Type 0: Not a Combination Product	07/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part332	03/02/2011

Labeler - ATLANTIC BIOLOGICALS CORP. (047437707)

Establishment
Name	Address	ID/FEI	Business Operations
ATLANTIC BIOLOGICALS CORP.		047437707	relabel(17856-5068) , repack(17856-5068)