Excedrin
- Product NDC
- 0067-2001
- 11-digit product format
- 000672001
- Labeler code
- 0067
- Product ID
- 0067-2001_155eb367-99df-1f50-e063-6294a90a21d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Aspirin (NSAID), and Caffeine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-03-15
- 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
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.
| Dataset | Scope | Package NDC |
|---|---|---|
| excluded product | product | |
| excluded package | package | 0067-2001-09 |
| excluded package | package | 0067-2001-05 |
| excluded package | package | 0067-2001-07 |
| excluded package | package | 0067-2001-03 |
| excluded package | package | 0067-2001-04 |
| excluded package | package | 0067-2001-08 |
| excluded package | package | 0067-2001-02 |
| excluded package | package | 0067-2001-06 |
| excluded package | package | 0067-2001-01 |
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
- Brand name suffix
- Extra Strength Pain Reliever
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 250 mg/1 |
| ASPIRIN | 250 mg/1 |
| CAFFEINE | 65 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
| R16CO5Y76E | Internal UNII lookup |
| 3G6A5W338E | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0067-2001-01 | ExcedrinExtra Strength Pain Reliever | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 10 | |
| 0067-2001-02 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-02 | ExcedrinExtra Strength Pain Reliever | 24 in 1 BOTTLE | TABLET, FILM COATED | 24 | 10 | |
| 0067-2001-03 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-03 | ExcedrinExtra Strength Pain Reliever | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 10 | |
| 0067-2001-04 | ExcedrinExtra Strength Pain Reliever | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | 10 | |
| 0067-2001-04 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-05 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-05 | ExcedrinExtra Strength Pain Reliever | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 10 | |
| 0067-2001-06 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-06 | ExcedrinExtra Strength Pain Reliever | 125 in 1 BOTTLE | TABLET, FILM COATED | 125 | 10 | |
| 0067-2001-07 | ExcedrinExtra Strength Pain Reliever | 200 in 1 BOTTLE | TABLET, FILM COATED | 200 | 10 | |
| 0067-2001-07 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-08 | ExcedrinExtra Strength Pain Reliever | 300 in 1 BOTTLE | TABLET, FILM COATED | 300 | 10 | |
| 0067-2001-08 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-09 | ExcedrinExtra Strength Pain Reliever | 250 in 1 BOTTLE | TABLET, FILM COATED | 250 | 10 | |
| 0067-2001-09 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 10 | |
| 0067-2001-14 | ExcedrinExtra Strength Pain Reliever | 8 in 1 VIAL | TABLET, FILM COATED | 8 | 10 | |
| 0067-2001-14 | ExcedrinExtra Strength Pain Reliever | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0067-2001 | EXCEDRIN EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN, ASPIRIN (NSAID), AND CAFFEINE) TABLET, FILM COATED [HALEON US HOLDINGS LLC] | 10 | Current NDC, Legacy NDC, 19 package rows | 20240407_1b5ff867-5442-4cf8-bd1e-530093cc88f8.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Acetaminophen Diphenhydramine HCL | ACETAMINOPHEN DIPHENHYDRAMINE HCL | WALGREENS CO. | d92d97a8-0ee3-1206-e053-2a95a90a72a8 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | SAM'S WEST INC | 0c8e7095-0806-4501-e063-6394a90a89aa | 2025-12-19 | Warnings | M013 |
| Acetaminophen Diphenhydramine HCL | ACETAMINOPHEN DIPHENHYDRAMINE HCL | WALGREEN CO. | b3763182-2428-155a-e053-2995a90ab578 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | WALGREENS | e467b78e-9f23-5563-e053-2a95a90a586e | 2025-12-19 | Warnings | M013 |
| Acetaminophen Diphenhydramine HCL | ACETAMINOPHEN DIPHENHYDRAMINE HCL | Walgreens | fd7c3250-35d4-494a-e053-6394a90a2db5 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | CVS PHARMACY, INC | 1ddb8a2b-3081-3eda-e063-6294a90ab82b | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | CVS PHARMACY, INC | b1307d52-10e6-46e1-e053-2995a90a03b6 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | CVS PHARMACY, INC | c2c6d6a1-b492-506d-e053-2995a90aac23 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | FAMILY DOLLAR | f8383108-0970-9f1e-e053-6294a90ad38f | 2025-12-19 | Warnings | M013 |
| ACETAMINOPHEN 500 MG | ACETAMINOPHEN | NUVICARE LLC | 591ee107-e953-4982-b75f-13a0afd7c4ae | 2025-12-19 | Warnings | M013 |
| Nuvicare Headache Relief | ACETAMINOPHEN, ASPIRIN, CAFFEINE | NUVICARE LLC | 3ede0fb6-c089-4253-9878-2b01c39e9c87 | 2025-12-19 | Warnings | M013 |
| Aspirin Low Dose | ASPIRIN | NUVICARE LLC | 3a4aa3c7-b726-4303-8803-74196fa5637a | 2025-12-19 | Warnings | M013 |
| ACETAMINOPHEN 500 MG | ACETAMINOPHEN | NUVICARE LLC | 95edf7bd-b6a7-4be5-9ad7-8748e7c2d06e | 2025-12-19 | Warnings | M013 |
| Pain Relief PM | ACETAMINOPHEN, DIPHENHYDRAMINE | NUVICARE LLC | 32a5611b-9bf6-4850-a7ff-fa240da04f45 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | BETTER LIVING BRANDS LLC. | ac0e96d0-746e-fb42-e053-2a95a90a1957 | 2025-12-18 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | BETTER LIVING BRANDS LLC. | ac0e5dc0-96eb-47b2-e053-2995a90add0e | 2025-12-18 | Warnings | M013 |
| Acetaminophen Diphenhydramine HCl | ACETAMINOPHEN DIPHENHYDRAMINE HCL | BETTER LIVING BRANDS LLC. | ac0f8d5c-d200-1156-e053-2a95a90aece6 | 2025-12-18 | Warnings | M013 |
| Pain and Fever Childrens | ACETAMINOPHEN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | e55645ab-66f9-4160-8247-395bc5b02711 | 2025-12-18 | Warnings | M013 |
| Dolex Forte | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Pharmadel LLC | 3c2d90fc-130d-476c-e063-6294a90a8c15 | 2025-12-17 | Warnings | M013 |
| CareOne Childrens Acetaminophen | ACETAMINOPHEN | American Sales Company | 07bc6632-fabb-427d-81f3-c27c54caa6a0 | 2025-12-17 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308297 | acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet | PSN | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 209468 | EXCEDRIN 250 MG / 250 MG / 65 MG Oral Tablet | PSN | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 209468 | acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet [Excedrin] | SBD | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 308297 | acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet | SCD | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 308297 | APAP 250 MG / ASA 250 MG / caffeine 65 MG Oral Tablet | SY | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 209468 | APAP 250 MG / ASA 250 MG / Caffeine 65 MG Oral Tablet [Excedrin] | SY | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 209468 | Excedrin Extra Strength (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet | SY | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 209468 | Excedrin Menstrual Complete (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet | SY | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 209468 | Excedrin Migraine (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet | SY | 1b5ff867-5442-4cf8-bd1e-530093cc88f8 | 10 |
| 308297 | acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet | PSN | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 209468 | EXCEDRIN 250 MG / 250 MG / 65 MG Oral Tablet | PSN | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 209468 | acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet [Excedrin] | SBD | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 308297 | acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet | SCD | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 308297 | APAP 250 MG / ASA 250 MG / caffeine 65 MG Oral Tablet | SY | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 209468 | APAP 250 MG / ASA 250 MG / Caffeine 65 MG Oral Tablet [Excedrin] | SY | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 209468 | Excedrin Extra Strength (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet | SY | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 209468 | Excedrin Menstrual Complete (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet | SY | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
| 209468 | Excedrin Migraine (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet | SY | f7e572e9-82a7-2127-e053-6394a90ab01a | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0067-2001-01 | 00067200101 | 2 TABLET, FILM COATED in 1 POUCH (0067-2001-01) | 2021-01-31 | 0000-00-00 | No | No | Current | |
| 0067-2001-02 | 00067200102 | 1 BOTTLE in 1 CARTON (0067-2001-02) / 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-09-30 | 0000-00-00 | No | No | Current |
| 0067-2001-03 | 00067200103 | 1 BOTTLE in 1 CARTON (0067-2001-03) / 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-09-30 | 0000-00-00 | No | No | Current |
| 0067-2001-04 | 00067200104 | 1 BOTTLE in 1 CARTON (0067-2001-04) / 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-09-30 | 0000-00-00 | No | No | Current |
| 0067-2001-05 | 00067200105 | 1 BOTTLE in 1 CARTON (0067-2001-05) / 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-03-15 | 0000-00-00 | No | No | Current |
| 0067-2001-06 | 00067200106 | 1 BOTTLE in 1 CARTON (0067-2001-06) / 125 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-09-30 | 0000-00-00 | No | No | Current |
| 0067-2001-07 | 00067200107 | 1 BOTTLE in 1 CARTON (0067-2001-07) / 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-09-30 | 0000-00-00 | No | No | Current |
| 0067-2001-08 | 00067200108 | 1 BOTTLE in 1 CARTON (0067-2001-08) / 300 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-03-15 | 0000-00-00 | No | No | Current |
| 0067-2001-09 | 00067200109 | 1 BOTTLE in 1 CARTON (0067-2001-09) / 250 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-09-30 | 0000-00-00 | No | No | Current |
| 0067-2001-14 | 00067200114 | 1 VIAL in 1 BLISTER PACK (0067-2001-14) / 8 TABLET, FILM COATED in 1 VIAL | 1 vial | 2021-01-31 | No | No | Current |