United States · FDA National Drug Code directory
TUMS ULTRA
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
- 0135-0180_5607f6ca-b124-ff93-e063-6394a90a6de3
- Product NDC
- 0135-0180
- Form
- TABLET, CHEWABLE
- Composition / generic term
- calcium carbonate
- Labeler
- Haleon US Holdings LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20100212
- Source listing expiry
- 20271231
Source-listed ingredients
- CALCIUM CARBONATE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 86 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-01) · 0135-0180-01
- 72 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-02) · 0135-0180-02
- 160 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-14) · 0135-0180-14
Source and coverage
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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.
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