Home NDC 73598-1372 Extra Strength Pain Reliever
Product NDC 73598-1372
11-digit product format 735981372
Labeler code 73598
Product ID 73598-1372_82d54d28-2fd1-44f4-ae89-5f23b79a37bd
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOPHEN, ASPIRIN, and CAFFEINE
Dosage form CAPSULE, COATED
Route ORAL
Labeler JHK Inc dba American Safety & First Aid
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2000-02-02
Substance ACETAMINOPHEN; ASPIRIN; CAFFEINE
Active strength 250; 250; 65 mg/1; mg/1; mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
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 · 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 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 73598-1372 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 73598-1372 73598-1372-1 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Extra Strength Pain Reliever
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 250 mg/1 ASPIRIN 250 mg/1 CAFFEINE 65 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup R16CO5Y76E Internal UNII lookup 3G6A5W338E Internal UNII 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 73598-1372-1 Extra Strength Pain Reliever 2 in 1 DOSE PACK CAPSULE, COATED 2 2 73598-1372-1 Extra Strength Pain Reliever 25 in 1 BOX CAPSULE, COATED 25 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73598-1372 EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) CAPSULE, COATED [JHK INC DBA AMERICAN SAFETY & FIRST AID] 2 Current NDC, Legacy NDC, 2 package rows 20240426_87c5ad71-0448-4e0f-acee-bf9a1d38675e.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 84 · 1,678 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 73598-1372-1 73598137201 25 DOSE PACK in 1 BOX (73598-1372-1) / 2 CAPSULE, COATED in 1 DOSE PACK 25 dose pack 2000-02-02 0000-00-00 No No Current