Label: MYLANTA NEW TONIGHT SOOTHING HONEY CHAMOMILE- calcium carbonate,magnesium hydroxide and simethicone suspension
- NDC Code(s): 62372-510-10, 62372-510-12
- Packager: Infirst Healthcare Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients (in each 10 mL dose)
- Purpose
- Uses
- Warnings
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Directions
- shake well before use
- measure with dosing cup provided
- adults and children 12 years and over: 10 mL-20 mL (1-2 doses) between meals, at bedtime or as directed by a doctor
- do not take more than 60 mL (6 doses) in any 24- hour period
- do not use the maximum dosage for more than 2 weeks
- children under 12 years: ask a doctor
- mL= milliliter
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
MYLANTA ®
LIQUID Tonight
ANTACID + ANTI-GAS
FAST RELIEF OF HEARTBURN AFTER DINNER
Soothing Honey Chamomile Flavor
12 FL OZ (355mL)
Mylanta Tonight, with its soothing honey- chamomile flavor, is perfect for fast heartburn relief in the evening-the time of day when adults suffer heartburn and acid indigestion the most.
Mylanta Tonight is also non–drowsy, so you can use it any time of the day. The great-tasting, soothing liquid, with extra coating power, helps make after-dinner heartburn feel better fast.
- Calcium-rich formula
- Paraben-free
- Smooth, creamy taste
Active ingredients: Calcium carbonate, Magnesium hydroxide, Simethicone
TAMPER-EVIDENT: DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING
Mylanta is a registered trademark of McNeil Consumer Pharmaceuticals Co.infirst +
HEALTHCARE
Manufactured for:
Infirst Healthcare Inc.
Westport, CT 06880
©2017 Infirst Healthcare Inc.
Mylanta.com
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INGREDIENTS AND APPEARANCE
MYLANTA NEW TONIGHT SOOTHING HONEY CHAMOMILE
calcium carbonate,magnesium hydroxide and simethicone suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62372-510 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 800 mg in 10 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE 270 mg in 10 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg in 10 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) GLYCERIN (UNII: PDC6A3C0OX) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) WATER (UNII: 059QF0KO0R) SODIUM CARBONATE (UNII: 45P3261C7T) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) SUCROSE (UNII: C151H8M554) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color white (OFF WHITE) Score Shape Size Flavor HONEY (CHAMOMILE) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62372-510-12 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/21/2016 2 NDC:62372-510-10 295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 03/21/2016 Labeler - Infirst Healthcare Inc. (079159739)