Data / Drug companies / Calcium carbonate, magnesium hydroxide and simethicone
Calcium carbonate, magnesium hydroxide and simethicone: 4 companies and 4 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Calcium carbonate, magnesium hydroxide and simethicone is listed in the FDA National Drug Code Directory by 4 companies, with 4 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are suspension; tablet, chewable, and the newest product started marketing on September 21, 2026.
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- Companies listing it
- 4
- Products
- 4
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Oral
- Brand names
- DG Health Liquid Antacid Plus Anti Gas, Kroger Liquid Antacid Plus Anti Gas, Rolaids Multi-Symptom Advanced Antacid Plus Anti-gas Wild Berry, Walgreen Liquid Antacid
- openFDA record search
- api.fda.gov
Companies that list calcium carbonate, magnesium hydroxide and simethicone
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Dolgencorp, Inc. (dollar General & Rexall) | 1 | suspension | Over the counter monograph drugs | March 17, 2025 |
| Kroger Company | 1 | suspension | Over the counter monograph drugs | September 21, 2026 |
| The Procter & Gamble Manufacturing Company | 1 | tablet, chewable | Over the counter monograph drugs | January 1, 2024 |
| Walgreen Company | 1 | suspension | Over the counter monograph drugs | October 1, 2024 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Suspension | 3 | 75% |
| Tablet, chewable | 1 | 25% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 4 | 100% |
Pharmacologic classes
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.