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Supreme Antacid

NDC 37808-614 · H E B

Generic namecalcium carbonate, magnesium hydroxide
Dosage formLIQUID
RouteORAL
Active ingredient(s)MAGNESIUM HYDROXIDE, CALCIUM CARBONATE
Strength800; 270 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], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

37808-614-05 — 355 mL in 1 BOTTLE (37808-614-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37808-136 — Calcium carbonate, 37808-137 — Calcium carbonate, 37808-203 — Calcium Carbonate, 37808-212 — Antacid Tablets, 37808-341 — Calcium carbonate, 37808-406 — calcium carbonate, 37808-493 — Calcium Carbonate, 37808-494 — Calcium Carbonate, 37808-503 — famotidine, calcium carbonate and magnesium hydroxide, 37808-554 — aluminum hydroxide, magnesium hydroxide, simethicone, 37808-638 — Calcium carbonate, 37808-889 — magnesium hydroxide, 37808-901 — magnesium hydroxide, 37808-936 — Calcium carbonate, 37808-938 — Calcium carbonate, 37835-115 — Calcium carbonate, 37835-126 — Calcium carbonate, 37835-127 — Calcium carbonate, 37835-171 — Calcium carbonate, 37835-184 — Calcium carbonate, +856 more

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