Home NDC 55910-204-30 Regular Strength Stomach Relief
Product NDC 55910-204
Requested package NDC 55910-204-30
11-digit product format 559100204
Labeler code 55910
Product ID 55910-204_2dc59956-7688-8fed-e063-6394a90af957
Type HUMAN OTC DRUG
Nonproprietary name Bismuth Subsalicylate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler DOLGENCORP, INC.
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-09-18
Substance BISMUTH SUBSALICYLATE
Active strength 262 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
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 · 3 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 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 55910-204 55910-204-30 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 55910-204 55910-204-30 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 55910-204 55910-204-30 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Regular Strength Stomach 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 308761 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 55910-204-30 Regular Strength Stomach Relief 5 in 1 CARTON TABLET, CHEWABLE 5 3 55910-204-30 Regular Strength Stomach Relief 6 in 1 CELLO PACK TABLET, CHEWABLE 6 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-204 REGULAR STRENGTH STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP, INC.] 3 Current NDC, 2 package rows 20250212_f2ec112f-213c-8a23-e053-2995a90a5f3f.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 · 228 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 55910-204-30 55910020430 5 CELLO PACK in 1 CARTON (55910-204-30) / 6 TABLET, CHEWABLE in 1 CELLO PACK 5 cello pack 2023-09-18 No No Current