United States · FDA National Drug Code directory
TUMS
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0135-1001_12c439c4-d4ad-fb8e-e063-6394a90aabd8
- Product NDC
- 0135-1001
- Form
- TABLET
- Composition / generic term
- calcium carbonate
- Labeler
- Haleon US Holdings LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20211008
- Source listing expiry
- 20261231
Source-listed ingredients
- CALCIUM CARBONATE — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 70 TABLET in 1 BOTTLE (0135-1001-01) · 0135-1001-01
- 96 TABLET in 1 BOTTLE (0135-1001-02) · 0135-1001-02
- 330 TABLET in 1 BOTTLE (0135-1001-03) · 0135-1001-03
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →