CVS Ultra Strength
- Product NDC
- 51316-031
- 11-digit product format
- 513160031
- Labeler code
- 51316
- Product ID
- 51316-031_4520d1c5-2b89-6314-e063-6294a90a661b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antacid Tablets
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- CVS
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-08-06
- Substance
- CALCIUM CARBONATE
- Active strength
- 1000 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CVS Ultra Strength
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51316-031-72 | CVS Ultra Strength | 72 in 1 BOTTLE | TABLET, CHEWABLE | 72 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51316-031 | CVS ULTRA STRENGTH (ANTACID TABLETS) TABLET, CHEWABLE [CVS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240817_6108271a-4336-4f90-9765-9c3aea109488.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51316-031-72 | 51316003172 | 72 TABLET, CHEWABLE in 1 BOTTLE (51316-031-72) | 2021-08-06 | 0000-00-00 | No | No | Current |