Home NDC 67751-155-01 Pepto Bismol
Product NDC 67751-155
Requested package NDC 67751-155-01
11-digit product format 677510155
Labeler code 67751
Product ID 67751-155_4efb4585-b90f-f303-e063-6294a90a4ba6
Type HUMAN OTC DRUG
Nonproprietary name BISMUTH SUBSALICYLATE
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Navajo Manufacturing Company Inc.
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-09-20
Substance BISMUTH SUBSALICYLATE
Active strength 262 mg/1
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 · 1 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 2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 67751-155 67751-155-01 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 Pepto Bismol
Listing expiration 2027-12-31 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 211151 Internal RxNorm lookup 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 67751-155-01 Pepto Bismol 1 in 1 CARTON TABLET, CHEWABLE 1 4 67751-155-01 Pepto Bismol 2 in 1 POUCH TABLET, CHEWABLE 2 4 67751-155-02 Pepto Bismol 1 in 1 CARTON TABLET, CHEWABLE 1 4 67751-155-02 Pepto Bismol 4 in 1 POUCH TABLET, CHEWABLE 4 4 67751-155-06 Pepto Bismol 2 in 1 POUCH TABLET, CHEWABLE 2 4 67751-155-06 Pepto Bismol 3 in 1 CARTON TABLET, CHEWABLE 3 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67751-155 PEPTO BISMOL (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [NAVAJO MANUFACTURING COMPANY INC.] 3 Current NDC, Legacy NDC, 6 package rows 20240417_033bccc6-6e81-487f-91fe-9d7cc465e1b2.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 67751-155-01 67751015501 1 POUCH in 1 CARTON (67751-155-01) / 2 TABLET, CHEWABLE in 1 POUCH 1 pouch 2016-09-20 0000-00-00 No No Current