Home NDC 73408-923 Thompson Cramp Relief
Product NDC 73408-923
11-digit product format 734080923
Labeler code 73408
Product ID 73408-923_47dff652-8219-2e89-e063-6294a90aad1f
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Pamabrom, Pyrilamine maleate
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Thompson Safety
Application M027
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-26
Substance ACETAMINOPHEN; PAMABROM; PYRILAMINE MALEATE
Active strength 500; 25; 15 mg/1; mg/1; mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 Thompson Cramp Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 PAMABROM 25 mg/1 PYRILAMINE MALEATE 15 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 UA8U0KJM72 Internal UNII lookup R35D29L3ZA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1052637 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73408-923-80 Thompson Cramp Relief 2 in 1 PACKET TABLET, FILM COATED 2 3 73408-923-80 Thompson Cramp Relief 40 in 1 BOX TABLET, FILM COATED 40 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73408-923 THOMPSON CRAMP RELIEF (ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE) TABLET, FILM COATED [THOMPSON SAFETY] 2 Current NDC, Legacy NDC, 2 package rows 20240117_e82f607d-05b1-2c50-e053-2995a90a607e.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 3 of 3 · 45 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Diurex Ultra CAFFEINE Kobayashi Healthcare International, Inc. 9a035265-40c6-43f5-8de6-6bece8449840 2025-04-14 Warnings Exact identifier application number: M027 Diurex Max PAMABROM Kobayashi Healthcare International, Inc. 37dfece3-d570-4ab2-ba95-af6eb1f3acd4 2025-04-11 Warnings Exact identifier application number: M027 Midol Complete ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE Bayer HealthCare LLC. ce9e6acb-a38b-4c9b-a7e8-3e1c2a49a324 2025-04-10 Warnings Exact identifier application number: M027 Diurex Water Pills CAFFEINE, MAGNESIUM SALICYLATE Kobayashi Healthcare International, Inc. e02a39f9-1c8c-4d38-b394-3f5b7062932c 2025-04-10 Warnings Exact identifier application number: M027 Cramp Tabs ACETAMINOPHEN, PAMABROM, AND PYRILAMINE MALEATE JHK DBA American Safety & First Aid c090807d-03b7-42d4-be41-f6240a3b330f 2024-10-04 Warnings Exact identifier application number: M027
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 73408-923-80 73408092380 40 PACKET in 1 BOX (73408-923-80) / 2 TABLET, FILM COATED in 1 PACKET 40 packet 2022-09-26 0000-00-00 No No Current