excedrin pm triple action caplets and excedrin extra strength pain reliever

Generic: acetaminophen, aspirin (nsaid), caffeine, and diphenhydramine citrate

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name excedrin pm triple action caplets and excedrin extra strength pain reliever
Generic Name acetaminophen, aspirin (nsaid), caffeine, and diphenhydramine citrate
Labeler haleon us holdings llc
Dosage Form KIT
Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-8148
Product ID 0067-8148_4b80de14-ddcc-e314-e063-6394a90aaa0f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2018-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00678148
Hyphenated Format 0067-8148

Supplemental Identifiers

RxCUI
209468 308297 1593110 1593116 2047427 2047428

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name excedrin pm triple action caplets and excedrin extra strength pain reliever (source: ndc)
Generic Name acetaminophen, aspirin (nsaid), caffeine, and diphenhydramine citrate (source: ndc)
Application Number M013 (source: ndc)

Resolved Composition

Strengths
  • 250 mg
  • 38 mg
  • 65 mg
source: label
Packaging
  • 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
source: ndc

Packages (1)

0067-8148-01 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

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "4b80de14-ddcc-e314-e063-6394a90aaa0f", "openfda": {"rxcui": ["209468", "308297", "1593110", "1593116", "2047427", "2047428"], "spl_set_id": ["444fa225-c204-45d1-b3b3-aa5650ee5d07"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "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", "package_ndc": "0067-8148-01", "marketing_start_date": "20180501"}], "brand_name": "Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever", "product_id": "0067-8148_4b80de14-ddcc-e314-e063-6394a90aaa0f", "dosage_form": "KIT", "product_ndc": "0067-8148", "generic_name": "Acetaminophen, Aspirin (NSAID), Caffeine, and Diphenhydramine Citrate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever", "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180501", "listing_expiration_date": "20271231"}