Home NDC 66715-9810 Excedrin Extra Strength
Product NDC 66715-9810
11-digit product format 667159810
Labeler code 66715
Product ID 66715-9810_458c59d3-e231-99ac-e063-6394a90ac131
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Aspirin, and Caffeine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Lil Drug Store Products, Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-05-10
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 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 Excedrin Extra Strength
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 3G6A5W338E Internal UNII lookup R16CO5Y76E Internal UNII lookup 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 209468 Internal RxNorm lookup 308297 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66715-9810-2 Excedrin Extra Strength 2 in 1 POUCH TABLET, FILM COATED 2 10 66715-9810-2 Excedrin Extra Strength 2 in 1 CARTON TABLET, FILM COATED 2 10 66715-9810-3 Excedrin Extra Strength 3 in 1 CARTON TABLET, FILM COATED 3 10 66715-9810-3 Excedrin Extra Strength 2 in 1 POUCH TABLET, FILM COATED 2 10 66715-9810-7 Excedrin Extra Strength 25 in 1 BOX, UNIT-DOSE TABLET, FILM COATED 25 10 66715-9810-7 Excedrin Extra Strength 2 in 1 POUCH TABLET, FILM COATED 2 10 66715-9810-8 Excedrin Extra Strength 30 in 1 CARTON TABLET, FILM COATED 30 10 66715-9810-8 Excedrin Extra Strength 2 in 1 POUCH TABLET, FILM COATED 2 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66715-9810 EXCEDRIN EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) TABLET, FILM COATED EXCEDRIN EXTRA STRENGTH, TRAVEL BASIX (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) TABLET, FILM COATED EXCEDRIN EXTRA STRENGTH, CVP HEALTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) TABLET, FILM COATED [LIL DRUG STORE PRODUCTS, INC] 9 Current NDC, Legacy NDC, 8 package rows 20241127_7f0f8b3c-c226-4a3a-af46-a708f345e4f5.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 37 of 79 · 1,570 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain Relief PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE TopCo Associates LLC 3b672ec7-8658-4b43-a79d-094ac8bc6904 2025-09-29 Warnings Exact identifier application number: M013 kirkland signature acetaminophen adult extra strength ACETAMINOPHEN Costco Wholesale Company a9979167-1a82-47d7-9602-2865f9bdd628 2025-09-27 Warnings Exact identifier application number: M013 First Aid Direct Chewable Aspirin ASPIRIN Cintas Corp ff6960f6-9f55-4f32-9ab5-9187724531e9 2025-09-25 Warnings Exact identifier application number: M013 Bayer Rapid Relief Body Pain ASPIRIN/CAFFEINE ORAL POWDER Bayer HealthCare LLC. 3fa1ec07-d1a6-226b-e063-6394a90a3213 2025-09-25 Warnings Exact identifier application number: M013 Xpect Chewable Aspirin ASPIRIN Cintas Corporation bddce374-1d35-4685-987d-4a4cc9994155 2025-09-25 Warnings Exact identifier application number: M013 IBUPROFEN IBUPROFEN Kroger Company bbedfc37-913d-8046-e053-2995a90af68a 2025-09-24 Warnings Exact identifier application number: M013 Xpect Pain Away Extra Strength ACETAMINOPHEN ASPIRIN CAFFEINE Cintas Corporation 1269d069-afaf-4ca5-b369-f74249a348db 2025-09-24 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN Preferred Pharmaceuticals Inc. 29214eec-860c-43f0-83c6-9ed5a9f530af 2025-09-22 Warnings Exact identifier application number: M013 ASPIRIN ASPIRIN Kroger Company bbee8ee4-e09d-3ba6-e053-2a95a90af647 2025-09-19 Warnings Exact identifier application number: M013 careone acetaminophen ACETAMINOPHEN American Sales Company 4bb696f6-a47b-4da9-9224-9aeae3e152f3 2025-09-19 Warnings Exact identifier application number: M013 Childrens Pain Relief ACETAMINOPHEN Aurohealth LLC 49a740ec-8ed4-4c76-b2d0-c13651bafa5e 2025-09-18 Warnings Exact identifier application number: M013 Extra Strength Headache Relief ACETAMINOPHEN, ASPIRIN, AND CAFFEINE Advanced Rx LLC a7ed4c76-a5b5-44f7-866f-f43790e45c78 2025-09-18 Warnings Exact identifier application number: M013 acetaminophen ACETAMINOPHEN CVS Pharmacy fc2d4367-8884-4b76-aa3e-8c35be1ace49 2025-09-18 Warnings Exact identifier application number: M013 Aspirin Enteric Coated, Regular Strength ASPIRIN Walgreen Company 5e1484d3-5be1-40da-a3bf-fb19f7d27d45 2025-09-18 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC ab02080a-c903-4e4a-a9f3-2b8197ed2f2b 2025-09-17 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 79669930-f744-4bb1-8325-b75951489b64 2025-09-17 Warnings Exact identifier application number: M013 Pain Reliever PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL L.N.K. International, Inc. ff199db8-c7ea-4b6e-ad8b-3ceeca883d92 2025-09-15 Warnings Exact identifier application number: M013 Acetaminophen PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL FOODHOLD U.S.A., LLC fdd7ce80-d6be-41b9-affd-d024cf306b50 2025-09-12 Warnings Exact identifier application number: M013 Extra Strength Pain Reliever ACETAMINOPHEN INGLES MARKETS, INC. 3e89240b-0e27-fde4-e063-6394a90a779f 2025-09-11 Warnings Exact identifier application number: M013 Aspirin 81 mg Low Dose ASPIRIN HEB 926fe7b6-9607-469f-912f-4019891067a9 2025-09-10 Warnings Exact identifier application number: M013
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 66715-9810-2 66715981002 2 POUCH in 1 CARTON (66715-9810-2) / 2 TABLET, FILM COATED in 1 POUCH 2 pouch 2016-02-04 0000-00-00 No No Current 66715-9810-3 66715981003 3 POUCH in 1 CARTON (66715-9810-3) / 2 TABLET, FILM COATED in 1 POUCH 3 pouch 2017-05-12 0000-00-00 No No Current 66715-9810-7 66715981007 25 POUCH in 1 BOX, UNIT-DOSE (66715-9810-7) / 2 TABLET, FILM COATED in 1 POUCH 25 pouch 2022-04-19 2028-09-11 No No Historical 66715-9810-8 66715981008 30 POUCH in 1 CARTON (66715-9810-8) / 2 TABLET, FILM COATED in 1 POUCH 30 pouch 2022-04-19 No No Current