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TUMS

NDC 0135-1000 · Haleon US Holdings LLC

Generic namecalcium carbonate
Dosage formTABLET
RouteORAL
Active ingredient(s)CALCIUM CARBONATE
Strength750 mg/1
Pharmacologic classBlood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
Marketing categoryOTC MONOGRAPH DRUG

Packages

0135-1000-01 — 70 TABLET in 1 BOTTLE (0135-1000-01)

0135-1000-02 — 96 TABLET in 1 BOTTLE (0135-1000-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0135-0606 — calcium carbonate, 0135-0611 — calcium carbonate, 0135-0618 — calcium carbonate, 0135-0623 — Calcium Carbonate, 0135-0624 — calcium carbonate and simethicone, 0135-0630 — calcium carbonate, 0135-0631 — calcium carbonate, 0135-0633 — calcium carbonate, 0135-0641 — calcium carbonate, 0135-0642 — calcium carbonate, 0135-1001 — calcium carbonate, 0135-1002 — calcium carbonate, 0135-1326 — calcium carbonate, 0135-1328 — calcium carbonate, 0135-5970 — calcium carbonate, 0280-0001 — Calcium Carbonate, 0280-0002 — calcium carbonate, 0280-0042 — Calcium carbonate, 0280-0051 — calcium carbonate and dimethicone, 0280-0058 — Calcium Carbonate, +648 more

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