Home NDC 70000-0044-2 Stomach Relief
Product NDC 70000-0044
Requested package NDC 70000-0044-2
11-digit product format 700000044
Labeler code 70000
Product ID 70000-0044_27ce7152-b2ea-4053-8cc6-2dd3e28b3be2
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form LIQUID
Route ORAL
Labeler Cardinal Health (Leader) 70000
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-02-25
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 70000-0044 70000-0044-2 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 70000-0044 70000-0044-2 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 Original 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 70000-0044-1 Stomach ReliefOriginal Strength 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 8 70000-0044-2 Stomach ReliefOriginal Strength 237 mL in 1 BOTTLE, PLASTIC LIQUID 237 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0044 STOMACH RELIEF ORIGINAL STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [CARDINAL HEALTH (LEADER) 70000] 4 Current NDC, Legacy NDC, 2 package rows 20240824_f1cbacb3-824b-4089-9da1-c4cf4bd27b99.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 70000-0044-2 70000004402 237 mL in 1 BOTTLE, PLASTIC (70000-0044-2) 237 ml 2020-02-25 0000-00-00 No No Current