Home NDC 21130-125 Digestive Relief
Product NDC 21130-125
11-digit product format 211300125
Labeler code 21130
Product ID 21130-125_424aa911-6748-010b-e063-6394a90a7ae7
Type HUMAN OTC DRUG
Nonproprietary name Bismuth Subsalicylate
Dosage form TABLET, FILM COATED
Route ORAL
Labeler SAFEWAY
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-10-05
Substance BISMUTH SUBSALICYLATE
Active strength 262 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
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 Digestive Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 262 mg/1
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 308760 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 21130-125-40 Digestive Relief 40 in 1 BOTTLE TABLET, FILM COATED 40 6 21130-125-40 Digestive Relief 1 in 1 CARTON TABLET, FILM COATED 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-125 DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) TABLET, FILM COATED [SAFEWAY] 5 Current NDC, Legacy NDC, 2 package rows 20241105_5538d56a-b258-4260-b51b-f5131bd76885.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 21130-125-40 21130012540 1 BOTTLE in 1 CARTON (21130-125-40) / 40 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2020-10-05 0000-00-00 No No Current