Home NDC 11822-1050 Rite Aid Extra Strength
Product NDC 11822-1050
11-digit product format 118221050
Labeler code 11822
Product ID 11822-1050_080fa9e6-b54a-4e61-81dd-fa36e1f303b5
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Hydroxide and Magnesium Carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler RITE AID CORPORATION
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-12-13
Substance ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
Active strength 160; 105 mg/1; mg/1
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 Extra Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 160 mg/1 MAGNESIUM CARBONATE 105 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup 0E53J927NA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308072 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11822-1050-0 Rite Aid Extra Strength 100 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-1050 RITE AID EXTRA STRENGTH (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) TABLET, CHEWABLE [RITE AID CORPORATION] 3 Current NDC, Legacy NDC, 1 package rows 20241101_d2f8dcc2-8833-4426-9c12-1a6087145122.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 10 of 34 · 675 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 11822-1050-0 11822105000 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11822-1050-0) 2022-12-13 0000-00-00 No No Current