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Brand-name over-the-counter medicine

Mylanta

Generic names: Calcium carbonate, dimethicone and magnesium hydroxide · Dimethicone · Aluminum hydroxide, dimethicone and magnesium hydroxide

Company: Infirst Healthcare Inc.

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Read the label on your package, and ask a pharmacist if you are not sure a medicine is right for you or your child.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Mylanta?
Mylanta is a brand name of Calcium carbonate, dimethicone and magnesium hydroxide, Dimethicone and Aluminum hydroxide, dimethicone and magnesium hydroxide, an over-the-counter medicine. The FDA NDC Directory lists 9 Mylanta products in 6 strengths and forms.
Who makes Mylanta?
Infirst Healthcare Inc. lists 8 of the 9 Mylanta products in the FDA NDC Directory.
Is there a generic or store brand of Mylanta?
Yes. The FDA NDC Directory lists 93 other products with the same active ingredients, strength and form as a Mylanta product, 93 of them generic or store brands. Ask your pharmacist whether one is right for you.
Has Mylanta been recalled?
No recall linked to Mylanta products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Mylanta is

Each Mylanta product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Calcium carbonate, dimethicone and magnesium hydroxide · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
calcium carbonate 1000 mg · dimethicone 80 mg · magnesium hydroxide 270 mg
tablet, chewable (oral)
Mylanta One Antacid/Anti-Gas None listed DailyMed
calcium carbonate 1200 mg/10 mL · dimethicone 80 mg/10 mL · magnesium hydroxide 270 mg/10 mL
liquid (oral)
Mylanta Coat and Cool None listed DailyMed
calcium carbonate 800 mg/10 mL · dimethicone 80 mg/10 mL · magnesium hydroxide 270 mg/10 mL
liquid (oral)
Mylanta Classic, Mylanta Vanilla Caramel 5 products, 3 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Calcium carbonate, dimethicone and magnesium hydroxide →

Dimethicone · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
dimethicone 125 mg
capsule, liquid filled (oral)
Mylanta Gas 45 products, 37 companies DailyMed
dimethicone 125 mg
tablet, chewable (oral)
Mylanta Gas Minis Assorted Fruit Flavor, Mylanta Gas Minis Mint Flavor 35 products, 31 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Dimethicone →

Aluminum hydroxide, dimethicone and magnesium hydroxide · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
aluminum hydroxide 800 mg/10 mL · dimethicone 80 mg/10 mL · magnesium hydroxide 800 mg/10 mL
suspension (oral)
Mylanta Maximum Strength Classic Flavor 8 products, 6 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Aluminum hydroxide, dimethicone and magnesium hydroxide →

FDA approval

Mylanta products are sold under an FDA over-the-counter monograph: rules that set the allowed active ingredients, strengths and label wording, so these products do not need an individual FDA approval.

Companies that list Mylanta

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Mylanta products.

  • Infirst Healthcare Inc.8 products
  • Infirst Healthcare1 product

Recalls

No recall linked to Mylanta products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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