excedrin pm triple action caplets and excedrin tension headache

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 tension headache
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 0067-8147
Product ID 0067-8147_5b0f5eff-6fa1-4334-a51c-fd79e54e209b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2017-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00678147
Hyphenated Format 0067-8147

Supplemental Identifiers

RxCUI
307686 404172 1593110 1593116

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 tension headache (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
  • 500 mg
  • 65 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE, COMBINATION (0067-8147-01) * 1 BOTTLE in 1 CARTON (0067-2056-24) / 24 TABLET, COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-8139-02) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

0067-8147-01 1 KIT in 1 PACKAGE, COMBINATION (0067-8147-01) * 1 BOTTLE in 1 CARTON (0067-2056-24) / 24 TABLET, COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-8139-02) / 100 TABLET, FILM COATED in 1 BOTTLE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Excedrin PM Triple Action Caplets and Excedrin Tension Headache ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "5b0f5eff-6fa1-4334-a51c-fd79e54e209b", "openfda": {"rxcui": ["307686", "404172", "1593110", "1593116"], "spl_set_id": ["978a9d27-6d41-42cb-a193-11314923d2ac"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0067-8147-01)  *  1 BOTTLE in 1 CARTON (0067-2056-24)  / 24 TABLET, COATED in 1 BOTTLE *  1 BOTTLE in 1 CARTON (0067-8139-02)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-8147-01", "marketing_start_date": "20170601"}], "brand_name": "Excedrin PM Triple Action Caplets and Excedrin Tension Headache", "product_id": "0067-8147_5b0f5eff-6fa1-4334-a51c-fd79e54e209b", "dosage_form": "KIT", "product_ndc": "0067-8147", "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 Tension Headache", "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170601", "listing_expiration_date": "20261231"}