Home NDC 21130-624-16 Stomach Relief
Product NDC 21130-624
Requested package NDC 21130-624-16
11-digit product format 211300624
Labeler code 21130
Product ID 21130-624_b797fd83-e9b6-43c2-9b78-b97767c341d1
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form LIQUID
Route ORAL
Labeler Safeway, Inc.
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-11-29
Substance BISMUTH SUBSALICYLATE
Active strength 525 mg/30mL
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
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 Stomach Relief
Brand name suffix Regular Strength
Listing expiration 2027-12-31 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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21130-624-08 Stomach ReliefRegular Strength 237 mL in 1 BOTTLE, PLASTIC LIQUID 237 3 21130-624-12 Stomach ReliefRegular Strength 355 mL in 1 BOTTLE, PLASTIC LIQUID 355 3 21130-624-16 Stomach ReliefRegular Strength 473 mL in 1 BOTTLE, PLASTIC LIQUID 473 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-624 STOMACH RELIEF REGULAR STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [SAFEWAY, INC.] 3 Current NDC, Legacy NDC, 3 package rows 20240516_2bde4e41-ffbd-4d9d-ae00-e39a5c7264b3.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 21130-624-16 21130062416 473 mL in 1 BOTTLE, PLASTIC (21130-624-16) 473 ml 2019-11-29 0000-00-00 No No Current