Home NDC 30142-138 Ultra Strength digestive relief
Product NDC 30142-138
11-digit product format 301420138
Labeler code 30142
Product ID 30142-138_3b873634-dbad-e0bc-e063-6294a90a5f74
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form TABLET
Route ORAL
Labeler THE KROGER CO.
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-11-18
Substance BISMUTH SUBSALICYLATE
Active strength 525 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 Ultra Strength digestive relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 525 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 1998447 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 30142-138-24 Ultra Strength digestive relief 1 in 1 CARTON TABLET 1 7 30142-138-24 Ultra Strength digestive relief 24 in 1 BOTTLE TABLET 24 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30142-138 ULTRA STRENGTH DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) TABLET [THE KROGER CO.] 6 Current NDC, Legacy NDC, 2 package rows 20240731_5e288108-1578-4379-a3d6-44b447187643.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 30142-138-24 30142013824 1 BOTTLE in 1 CARTON (30142-138-24) / 24 TABLET in 1 BOTTLE 1 bottle 2019-11-18 0000-00-00 No No Current