MYLANTA GAS  MAXIMUM STRENGTH- dimethicone tablet, chewable 
McNeil Consumer Pharmaceuticals Co.

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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Mylanta®
Gas

Drug Facts

Active ingredient (in each tablet)

Simethicone 125 mg

Purpose

Antigas

Use

  • relieves bloating, pressure, and discomfort of gas which can be caused by certain foods (such as beans, bran, and broccoli) or air swallowing

Warnings

Keep out of reach of children.

Directions

  • thoroughly chew 1-2 tablets as needed after meals and at bedtime
  • do not exceed 4 tablets per day unless directed by a physician

Other information

  • each tablet contains: calcium 66 mg
  • store between 20-25°C (68-77°F). Avoid high humidity.
  • do not use if carton or any blister unit is open or broken

Inactive ingredients

D&C red no. 7 calcium lake, dextrates, flavors, magnesium stearate, modified starch, silicon dioxide, tribasic calcium phosphate

Questions or comments?

call 1-800-469-5268 (toll-free) or 215-273-8755 (collect)

PRINCIPAL DISPLAY PANEL

NDC 16837-861-24

Mylanta®
Gas

SIMETHICONE • ANTI-GAS

MAXIMUM
STRENGTH

Fast Acting

  • Pressure
  • Bloating
  • Discomfort

CHERRY
Chewable Tablets

24 TABLETS-125 mg each

Principal Display Panel
MYLANTA GAS   MAXIMUM STRENGTH
dimethicone tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16837-861
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O) Dimethicone125 mg
Inactive Ingredients
Ingredient NameStrength
DEXTRATES (UNII: G263MI44RU)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
Product Characteristics
ColorPINKScore2 pieces
ShapeROUNDSize16mm
FlavorCHERRYImprint Code MYL;GAS;125
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:16837-861-244 in 1 CARTON
16 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33206/01/199606/30/2015
Labeler - McNeil Consumer Pharmaceuticals Co. (160159638)

Revised: 4/2015
 
McNeil Consumer Pharmaceuticals Co.