NDC 85237-1868-01 - Excedrin Extra Strength Headache
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 85237-1868
- Requested NDC
- 85237-1868-01
- Package NDCs from labels
- 85237-1868-1, 85237-1868-2, 85237-1868-3, 85237-1868-6, 85237-1868-01
- Manufacturer
- Select Consumer Group
- Effective date
- 2026-10-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Excedrin Extra Strength Headache - Select Consumer Group | Select Consumer Group | 2026-10-24 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85237-1868-1 | ExcedrinExtra Strength Headache | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | 3 | |
| 85237-1868-1 | ExcedrinExtra Strength Headache | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 3 | |
| 85237-1868-2 | ExcedrinExtra Strength Headache | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 3 | |
| 85237-1868-2 | ExcedrinExtra Strength Headache | 2 in 1 BLISTER PACK | TABLET, FILM COATED | 2 | 3 | |
| 85237-1868-3 | ExcedrinExtra Strength Headache | 25 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 25 | 3 | |
| 85237-1868-3 | ExcedrinExtra Strength Headache | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 3 | |
| 85237-1868-6 | ExcedrinExtra Strength Headache | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 3 | |
| 85237-1868-6 | ExcedrinExtra Strength Headache | 50 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 50 | 3 |
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 |
|---|---|---|---|---|---|---|
| BUTALBITAL and ACETAMINOPHEN | BUTALBITAL AND ACETAMINOPHEN | QUAGEN PHARMACEUTICALS LLC | 1f0dbe62-6aea-4323-ad25-c2211f919253 | 2024-05-06 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| BUTALBITAL, ACETAMINOPHEN AND CAFFEINE | BUTALBITAL, ACETAMINOPHEN AND CAFFEINE | QUAGEN PHARMACEUTICALS LLC | 24813ec6-0111-4782-9182-a2b93501a2bc | 2024-05-06 | Boxed warning, Warnings, Adverse reactions | 3G6A5W338E 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | Baxter Healthcare Corporation | 0f67c1bd-915b-4681-88dd-22f5154a80b3 | 2024-05-06 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Basic Care Childrens Pain and Fever | ACETAMINOPHEN | Amazon.com Services LLC | bf8bed5d-7dd4-492c-98ac-c36ff8be8f41 | 2024-05-06 | Warnings | M013 362O9ITL9D |
| Basic Care Childrens Pain and Fever | ACETAMINOPHEN | Amazon.com Services LLC | 0c133707-a8b8-4105-82f3-e3855ec19617 | 2024-05-06 | Warnings | M013 362O9ITL9D |
| leader infants pain and fever | ACETAMINOPHEN | Cardinal Health 110, LLC. dba Leader | cfbb8553-f3ac-437d-8f63-caa93f257a77 | 2024-05-06 | Warnings | M013 362O9ITL9D |
| LOW DOSE ASPIRIN | ASPIRIN | Bryant Ranch Prepack | a272bf44-54df-448a-8bff-e31f9488b416 | 2024-05-06 | Warnings | M013 R16CO5Y76E |
| BUTALBITAL and ACETAMINOPHEN | BUTALBITAL AND ACETAMINOPHEN | QUAGEN PHARMACEUTICALS LLC | 2eb09253-7f59-401e-afbc-70bb9600fedf | 2024-05-06 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| good sense childrens pain and fever | ACETAMINOPHEN | L. Perrigo Company | ab96395c-a19e-40d6-b37e-7f988026fc95 | 2024-05-06 | Warnings | M013 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | WALGREEN CO. | c20d110a-ed5e-aed4-e053-2a95a90a4200 | 2024-05-06 | Warnings | 362O9ITL9D |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Kroger | 1014da86-3a0e-136f-e063-6294a90ac931 | 2024-05-04 | Warnings | 362O9ITL9D |
| Theraflu-D Flu Relief Max Strength plus Nasal Decongestant | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PSEUDOEPHEDRINE HCL | Haleon US Holdings LLC | e35cb719-9e7d-4b2b-81a4-29e147dd74fa | 2024-05-03 | Warnings | 362O9ITL9D |
| Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PSEUDOEPHEDRINE HCL | Haleon US Holdings LLC | 09e20842-2b75-43b9-ae5f-3515b35e655b | 2024-05-03 | Warnings | 362O9ITL9D |
| Cold and Flu Relief | ACETAMINOPHEN DEXTROMETHORPHAN HBR PHENYLEPHRINE HCL | Family Dollar (FAMILY WELLNESS) | f958d8ba-ede9-4b1a-8317-2404b68a9129 | 2024-05-03 | Warnings | 362O9ITL9D |
| Enviroclenz | BERBERIS VULGARIS, CARDUUS MARIANUS, CHELIDONIUM MAJUS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, STILLINGIA SYLVATICA, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE, GERMANIUM SESQUIOXIDE, PHYTOLACCA DECANDRA, ACETONE, AMMONIUM MURIATICUM, BENZINUM, PROPYLENE GLYCOL, SODIUM LAURYL SULFATE, SODIUM TRIPOLYPHOSPHATE, TEREBINTHINA, METHANOL, CHLORINUM, IRIDIUM METALLICUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM | Deseret Biologicals, Inc. | 92816bbe-96d6-45fc-9929-d3e6df394a33 | 2024-05-02 | Warnings | 6DC9Q167V3 368GB5141J |
| Night Time Cold and Flu Relief Multi Symptom | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | 07c7c0d9-f063-4efc-8a08-2a1bfa9ca84a | 2024-05-01 | Warnings | 362O9ITL9D |
| Night Time Cold and Flu Multi Symptom | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | dbfb8971-a122-4a97-a665-e3f0d494876e | 2024-05-01 | Warnings | 362O9ITL9D |
| Daytime Cold and Flu Non Drowsy | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | P & L Development, LLC | c08b150c-d821-466c-8521-f77535d6af1e | 2024-04-30 | Warnings | 362O9ITL9D |
| Good Sense pain and fever | ACETAMINOPHEN | L. Perrigo Company | 48833e6a-db42-42b8-aa75-07103a1482a2 | 2024-04-30 | Warnings | M013 362O9ITL9D |
| basic care infants pain and fever | ACETAMINOPHEN | Amazon.com Services LLC | aaa2b462-5ccf-43b0-9d71-71de74653a21 | 2024-04-29 | Warnings | M013 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.