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ANTACID AND ANTIGAS

NDC 57896-662 · Geri-Care Pharmaceuticals, Corp

Generic namecalcium carbonate, magnesium hydroxide, simethicone
Dosage formLIQUID
RouteORAL
Active ingredient(s)CALCIUM CARBONATE, DIMETHICONE, MAGNESIUM HYDROXIDE
Strength800; 80; 270 mg/10mL; mg/10mL; mg/10mL
Pharmacologic classBlood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

57896-662-12 — 355 mL in 1 BOTTLE (57896-662-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

57896-615 — magnesium hydroxide, 57896-619 — aluminum hydroxide, magnesium hydroxide, dimethicone, 57896-624 — calcium carbonate, magnesium hydroxide, 57896-629 — aluminum hydroxide, magnesium hydroxide, dimethicone, 57896-638 — aluminum hydroxide, magnesium hydroxide, dimethicone, 57896-639 — aluminum hydroxide, magnesium hydroxide, dimethicone, 57896-647 — magnesium hydroxide, 57896-648 — magnesium hydroxide, 57896-649 — magnesium hydroxide, 57896-655 — calcium carbonate, magnesium hydroxide, simethicone, 57896-664 — aluminum hydroxide, magnesium hydroxide, dimethicone, 57896-666 — calcium carbonate, magnesium hydroxide, simethicone, 57896-694 — Simethicone, 57896-763 — calcium carbonate, 57896-791 — Simethicone, 57896-798 — Simethicone, 58228-0091 — Calcium Carbonate, 58602-815 — Loperamide Hydrochloride and Simethicone, 58602-868 — Loperamide Hydrochloride and Simethicone, 58602-869 — Loperamide Hydrochloride and Simethicone, +1295 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels