Label: MYLANTA GAS MINIS ASSORTED FRUIT FLAVOR- simethicone tablet, chewable
- NDC Code(s): 62372-801-03, 62372-801-50, 62372-801-60
- Packager: Infirst Healthcare Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 4, 2023
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- Drug Facts
- Active ingredient (in each 3 tablet dose)
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
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Mylanta ®
GAS Minis
- Fast relief of the bloating , pressure, and discomfort of gas
- Extra Strength, with the #1 selling medicine for gas relief
- Great tasting ,chewable mini-tablets in an on-the-go pack
- Also available in great tasting Arctic Mint & Cherry
TAMPER EVIDENT: DO NOT USE MYLANTA GAS MINI-TABLETS IF THE BREAKAWAY BAND ON TOP OF CONTAINER IS BROKEN OR MISSING.
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Mylanta is a registered trademark of McNeil Consumer Pharmaceuticals Co.
Patent pending
infirst +
HEALTHCARE
Manufactured for:
Infirst Healthcare Inc.
Westport, CT 06880
©2016 Infirst Healthcare Inc.
Mylanta.com
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INGREDIENTS AND APPEARANCE
MYLANTA GAS MINIS ASSORTED FRUIT FLAVOR
simethicone tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62372-801 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 125 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) D&C RED NO. 27 (UNII: 2LRS185U6K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P) ISOMALT (UNII: S870P55O2W) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SUCRALOSE (UNII: 96K6UQ3ZD4) SUCROSE (UNII: C151H8M554) TRICALCIUM PHOSPHATE (UNII: K4C08XP666) Product Characteristics Color pink (LIGHT) , orange, purple Score no score Shape OVAL (OBLONG) Size 12mm Flavor FRUIT (ASSORTED) Imprint Code MYLG Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62372-801-50 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/21/2016 06/01/2023 2 NDC:62372-801-60 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/21/2016 3 NDC:62372-801-03 3 in 1 POUCH; Type 0: Not a Combination Product 10/04/2019 06/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M002 03/21/2016 Labeler - Infirst Healthcare Inc. (079159739)