Home NDC 37000-537 Pepto Bismol
Product NDC 37000-537
11-digit product format 370000537
Labeler code 37000
Product ID 37000-537_e4f32d6f-5f88-f7a8-e053-2995a90a4fee
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler The Procter & Gamble Manufacturing Company
Application M008
Marketing category OTC MONOGRAPH FINAL
Marketing start 2018-03-01
Marketing end 0000-00-00
Substance BISMUTH SUBSALICYLATE
Active strength 262 mg/1
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 37000-537-12 Pepto BismolDiarrhea Liquicaps 1 in 1 CARTON CAPSULE, LIQUID FILLED 1 10 37000-537-12 Pepto BismolDiarrhea Liquicaps 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 10 37000-537-24 Pepto BismolDiarrhea Liquicaps 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 10 37000-537-24 Pepto BismolDiarrhea Liquicaps 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 10 37000-537-48 Pepto BismolDiarrhea Liquicaps 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 10 37000-537-48 Pepto BismolDiarrhea Liquicaps 4 in 1 CARTON CAPSULE, LIQUID FILLED 4 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37000-537 PEPTO BISMOL DIARRHEA LIQUICAPS (BISMUTH SUBSALICYLATE) CAPSULE, LIQUID FILLED [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 10 Legacy NDC, 6 package rows 20231129_851997d7-cb82-17bf-e053-2a91aa0ab78b.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 4 of 10 · 198 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 37000-537-12 37000053712 1 BLISTER PACK in 1 CARTON (37000-537-12) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 1 blister pack 2019-03-01 0000-00-00 No No Current 37000-537-24 37000053724 2 BLISTER PACK in 1 CARTON (37000-537-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 2 blister pack 2019-03-01 0000-00-00 No No Current 37000-537-48 37000053748 4 BLISTER PACK in 1 CARTON (37000-537-48) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 4 blister pack 2019-03-01 0000-00-00 No No Current