Ultra Strength
- Product NDC
- 21130-031
- 11-digit product format
- 211300031
- Labeler code
- 21130
- Product ID
- 21130-031_424a162b-7e6b-5083-e063-6294a90ae5af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antacid Tablets
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- SAFEWAY
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-10-05
- 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
- 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 |
|---|
| 21130-031-72 | Ultra Strength | 72 in 1 BOTTLE | TABLET, CHEWABLE | 72 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-031 | ULTRA STRENGTH (ANTACID TABLETS) TABLET, CHEWABLE [SAFEWAY] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241102_4c6cdd81-5145-4a1f-888f-85cf5d856c39.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 |
|---|
| 21130-031-72 | 21130003172 | 72 TABLET, CHEWABLE in 1 BOTTLE (21130-031-72) | 2020-10-05 | 0000-00-00 | No | No | Current |