TUMS
- Product NDC
- 0135-0221
- 11-digit product format
- 001350221
- Labeler code
- 0135
- Product ID
- 0135-0221_4e6d1e5b-2025-907d-e063-6294a90abe8c
- 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
- 2026-04-01
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| H0G9379FGK | CALCIUM CARBONATE | 471-34-1 | CALCIUM CARBONATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0135-0221-01 | 00135022101 | 236 TABLET, CHEWABLE in 1 BOTTLE (0135-0221-01) | 2026-04-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | Haleon US Holdings LLC | 2026-04-01 | HUMAN OTC DRUG LABEL | 21 |