Home NDC 73598-1232 PEPT-ACHE
Product NDC 73598-1232
11-digit product format 735981232
Labeler code 73598
Product ID 73598-1232_d994e7c7-adc5-4ab7-a89a-318ea09b2bb1
Type HUMAN OTC DRUG
Nonproprietary name BISMUTH SUBSALICYLATE
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler JHK Inc dba American Safety & First Aid
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2000-02-02
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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 73598-1232-1 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 73598-1232-1 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 PEPT-ACHE
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 73598-1232-1 PEPT-ACHE 1 in 1 PACKET TABLET, CHEWABLE 1 2 73598-1232-1 PEPT-ACHE 36 in 1 BOX TABLET, CHEWABLE 36 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73598-1232 PEPT-ACHE (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [JHK INC DBA AMERICAN SAFETY & FIRST AID] 2 Current NDC, Legacy NDC, 2 package rows 20240522_894c1912-cd24-4ddf-b7e7-dae9dd64b280.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 73598-1232-1 73598123201 36 PACKET in 1 BOX (73598-1232-1) / 1 TABLET, CHEWABLE in 1 PACKET 36 packet 2000-02-02 0000-00-00 No No Current