Label: MYLANTA CLASSIC- calcium carbonate, magnesium hydroxide, simethicone liquid
- NDC Code(s): 62372-501-12
- Packager: Infirst Healthcare Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 5, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purposes
- 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) as needed, 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?
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INGREDIENTS AND APPEARANCE
MYLANTA CLASSIC
calcium carbonate, magnesium hydroxide, simethicone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62372-501 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 800 mg in 10 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg in 10 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE 270 mg in 10 mL Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) BENZYL ALCOHOL (UNII: LKG8494WBH) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H) PEG-8 STEARATE (UNII: 2P9L47VI5E) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBIC ACID (UNII: X045WJ989B) SUCRALOSE (UNII: 96K6UQ3ZD4) POLYSORBATE 65 (UNII: 14BGY2Y3MJ) EDETATE DISODIUM (UNII: 7FLD91C86K) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color white Score Shape Size Flavor LEMON (Mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62372-501-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 01/31/2024 Labeler - Infirst Healthcare Inc. (079159739)