Mejoral
- Product NDC
- 69729-154
- 11-digit product format
- 697290154
- Labeler code
- 69729
- Product ID
- 69729-154_30b68c1e-b60f-4e36-e063-6294a90a77dc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Caffeine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- OPMX LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-12-05
- Substance
- ACETAMINOPHEN; CAFFEINE
- Active strength
- 500; 65 mg/1; mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [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.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 69729-154-24 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 69729-154-24 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 69729-154-24 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 69729-154-24 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 69729-154-24 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
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
- Mejoral
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
| CAFFEINE | 65 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
| 3G6A5W338E | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 307686 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 0bccf571-fcb9-2dd5-e063-6294a90a5f16 | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69729-154-24 | 2025-03-19 | C162847 | 48780-1 | 2cef2736-763c-d83d-e063-dadaa90ab31f | Mejoral |
| 69729-154-24 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-763c-d83d-e063-dadaa90ab31f | Mejoral |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69729-154-24 | Mejoral | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 2 | |
| 69729-154-24 | Mejoral | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 2 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| MAXIMUM STRENGTH NON-ASPIRIN 100 | ACETAMINOPHEN | JHK Inc dba American Safety & First Aid | 1d3e9948-883e-4668-9bb8-d699a283b51a | 2025-12-16 | Warnings | M013 |
| TYLENOL EXTRA STRENGTH, TRAVEL BASIX | ACETAMINOPHEN | Lil' Drug Store Products, Inc. | fa951d50-b79c-4161-8c81-fcf386b0964e | 2025-12-15 | Warnings | M013 |
| Vanquish Extra Strength | ACETAMINOPHEN, ASPIRIN, AND CAFFEINE | DSE Healthcare Solutions, LLC | cbf12223-ef44-494b-9d3c-971dce3c5ade | 2025-12-15 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 8bc75bcf-01c9-41d0-a96f-77a24e3edf01 | 2025-12-15 | Warnings | M013 |
| Pain Reliever | ACETAMINOPHEN | WALGREENS | 40a1b354-9b2e-1cf3-e063-6394a90af113 | 2025-12-13 | Warnings | M013 |
| topcare childrens pain and fever | ACETAMINOPHEN | Topco Associates LLC | 911492d5-e065-4b8f-b2dc-cb6a6678d0ae | 2025-12-13 | Warnings | M013 |
| Pain Reliever, Extra Strength, 24-7 Life by 7-Eleven | ACETAMINOPHEN TABLET | Lil' Drug Store Products, Inc. | 45c397bd-a1ff-1246-e063-6394a90ac54a | 2025-12-12 | Warnings | M013 |
| Pain Reliever PM, Extra Strength, 24-7 Life by 7-Eleven | ACETAMINOPHEN, DIPHENHYDRAMINE HCL TABLET, FILM COATED | Lil' Drug Store Products, Inc. | 45c7c11b-d627-aee8-e063-6294a90a401d | 2025-12-12 | Warnings | M013 |
| Aspirin | ASPIRIN | TOP CARE (Topco Associates LLC) | d3df90be-9037-44b2-bf48-540d68a033b2 | 2025-12-12 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | Hy-Vee | 98ab6fb7-c7e5-45ab-97c3-81d422f8a843 | 2025-12-11 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | PAI Holdings, LLC dba PAI Pharma | 33599f18-5f49-4f22-8a77-a072115763ef | 2025-12-11 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 746059b3-ed18-4a81-a70e-4d758e048d8e | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | f8820150-feec-4062-85bb-14525ddf691f | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 005e299e-aa84-49d9-bbca-12236f865a27 | 2025-12-11 | Warnings | M013 |
| Low Dose Chewable Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 7d88f156-d361-4249-b70d-4bbcd5ba30b7 | 2025-12-11 | Warnings | M013 |
| Enteric Coated Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | cc18e8e1-652e-44da-a9d7-e56cebda55a1 | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | d4c32e70-778a-4d66-b9d0-03944a528421 | 2025-12-11 | Warnings | M013 |
| adult low dose aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 6fa1c707-bd42-455b-90a3-2c2a11acc683 | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 5a80cb17-7731-4457-acd3-64cf4accf862 | 2025-12-11 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 02e3798f-86d9-64b4-e063-6294a90a29de | 2025-12-11 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 307686 | acetaminophen 500 MG / caffeine 65 MG Oral Tablet | PSN | 0bccf571-fcb9-2dd5-e063-6294a90a5f16 | 2 |
| 307686 | acetaminophen 500 MG / caffeine 65 MG Oral Tablet | SCD | 0bccf571-fcb9-2dd5-e063-6294a90a5f16 | 2 |
| 307686 | APAP 500 MG / Caffeine 65 MG Oral Tablet | SY | 0bccf571-fcb9-2dd5-e063-6294a90a5f16 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 69729-154-24 | 69729015424 | 2 BLISTER PACK in 1 CARTON (69729-154-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2023-12-05 | No | No | Current |