Tums
- Product NDC
- 0135-1327
- 11-digit product format
- 001351327
- Labeler code
- 0135
- Product ID
- 0135-1327_5aac471f-ca41-1ed3-e063-6394a90ae8bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-18
- Substance
- CALCIUM CARBONATE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tums
- Brand name suffix
- Chewy Bites Cherries and Watermelon
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CALCIUM CARBONATE | 750 mg/1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 0135-1327-60 | 00135132760 | 60 TABLET, CHEWABLE in 1 BOTTLE (0135-1327-60) | 2026-09-18 | No | No | Current |