Home NDC 0067-8148-01 Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever
Product NDC 0067-8148
Requested package NDC 0067-8148-01
11-digit product format 000678148
Labeler code 0067
Product ID 0067-8148_4b80de14-ddcc-e314-e063-6394a90aaa0f
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Aspirin (NSAID), Caffeine, and Diphenhydramine Citrate
Dosage form KIT
Labeler Haleon US Holdings LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-05-01
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 2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 0067-8148 0067-8148-01 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…
Additional Listing Data#
Finished product Yes
Brand name base Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever
Listing expiration 2027-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 6 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 209468 Internal RxNorm lookup 308297 Internal RxNorm lookup 1593110 Internal RxNorm lookup 1593116 Internal RxNorm lookup 2047427 Internal RxNorm lookup 2047428 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 0067-2000-91 Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever 100 in 1 BOTTLE TABLET, FILM COATED 100 250 mg 6 0067-2000-91 Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever 1 in 1 CARTON TABLET, FILM COATED 65 mg 6 0067-2056-24 Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever 24 in 1 BOTTLE TABLET, COATED 24 250 mg 6 0067-2056-24 Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever 1 in 1 CARTON TABLET, COATED 38 mg 6 0067-8148-01 Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever 1 in 1 PACKAGE, COMBINATION KIT 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0067-8148 EXCEDRIN PM TRIPLE ACTION CAPLETS AND EXCEDRIN EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN, ASPIRIN (NSAID), CAFFEINE, AND DIPHENHYDRAMINE CITRATE) KIT [HALEON US HOLDINGS LLC] 5 Current NDC, Legacy NDC, 5 package rows 20240316_444fa225-c204-45d1-b3b3-aa5650ee5d07.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.
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 0067-8148-01 00067814801 1 KIT in 1 PACKAGE, COMBINATION (0067-8148-01) * 1 BOTTLE in 1 CARTON (0067-2056-24) / 24 TABLET, COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-2000-91) / 100 TABLET, FILM COATED in 1 BOTTLE 1 kit 2018-05-01 0000-00-00 No No Current