Rite Aid Ultra Strength
- Product NDC
- 11822-0312
- 11-digit product format
- 118220312
- Labeler code
- 11822
- Product ID
- 11822-0312_edbe4b75-e830-4e09-bb65-bb343c533280
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- RITE AID CORPORATION
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-03-13
- 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
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 |
|---|
| 11822-0312-7 | 11822031207 | 72 TABLET, CHEWABLE in 1 BOTTLE (11822-0312-7) | 2019-03-13 | No | No | Historical |