Tums
- Product NDC
- 0135-0553
- 11-digit product format
- 001350553
- Labeler code
- 0135
- Product ID
- 0135-0553_80b36d79-a112-426a-ae40-5c4371258157
- 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
- 2023-03-01
- Substance
- CALCIUM CARBONATE
- Active strength
- 1000 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tums
- Brand name suffix
- Ultra
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM CARBONATE | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H0G9379FGK |
| Rxcui | 308892, 1044524 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0135-0553-01 | TumsUltra | 72 in 1 BOTTLE | TABLET, CHEWABLE | 72 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0135-0553 | TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC] | 4 | Current NDC, 1 package rows | 20250228_c544120f-15f0-48b5-88b2-d4820f180f50.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0135-0553-01 | 00135055301 | 72 TABLET, CHEWABLE in 1 BOTTLE (0135-0553-01) | 2023-03-01 | No | No | Historical |