Home NDC 11822-2910 Stomach Relief
Product NDC 11822-2910
11-digit product format 118222910
Labeler code 11822
Product ID 11822-2910_0dbc9d1a-f77d-4ad8-8838-30190aa0a71e
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form LIQUID
Route ORAL
Labeler Rite Aid Corporation
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-12-27
Marketing end 2026-12-27
Substance BISMUTH SUBSALICYLATE
Active strength 525 mg/30mL
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
NDC exclude flag No
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 Stomach Relief
Brand name suffix Regular Strength Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 525 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 62TEY51RR1 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308762 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11822-2910-7 Stomach ReliefRegular Strength 473 mL in 1 BOTTLE, PLASTIC LIQUID 473 6 11822-2910-8 Stomach ReliefRegular Strength 237 mL in 1 BOTTLE, PLASTIC LIQUID 237 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-2910 STOMACH RELIEF REGULAR STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [RITE AID CORPORATION] 5 Current NDC, Legacy NDC, 2 package rows 20240514_e9f5b3c3-9585-448d-8134-2214b5d78db0.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 1 of 12 · 223 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11822-2910-7 11822291007 473 mL in 1 BOTTLE, PLASTIC (11822-2910-7) 473 ml 2019-12-27 2026-12-27 No No Current 11822-2910-8 11822291008 237 mL in 1 BOTTLE, PLASTIC (11822-2910-8) 237 ml 2019-12-27 2026-12-27 No No Current