Home NDC 11822-0312 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 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Rite Aid Ultra Strength
Brand name suffix Peppermint Flavor
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1000 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308892 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11822-0312-7 Rite Aid Ultra StrengthPeppermint Flavor 72 in 1 BOTTLE TABLET, CHEWABLE 72 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-0312 RITE AID ULTRA STRENGTH PEPPERMINT FLAVOR (CALCIUM CARBONATE) TABLET, CHEWABLE [RITE AID CORPORATION] 7 Current NDC, Legacy NDC, 1 package rows 20241101_4e963099-fd7f-4862-9f9c-9f1fb963779e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 8 of 34 · 678 matching rows.
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 11822-0312-7 11822031207 72 TABLET, CHEWABLE in 1 BOTTLE (11822-0312-7) 2019-03-13 0000-00-00 No No Current