Acetaminophen
- Product NDC
- 69842-298
- 11-digit product format
- 698420298
- Labeler code
- 69842
- Product ID
- 69842-298_04020582-1e29-0e5d-e063-6394a90a3b90
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CVS PHARMACY, INC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-01
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- 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 | 69842-298-60 |
| excluded package | package | 69842-298-30 |
| excluded package | package | 69842-298-10 |
| excluded package | package | 69842-298-40 |
| excluded package | package | 69842-298-05 |
| excluded package | package | 69842-298-24 |
| excluded package | package | 69842-298-21 |
| excluded package | package | 69842-298-15 |
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
- Acetaminophen
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 198440 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 852e70e2-7279-6f33-e053-2991aa0a8676 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69842-298-05 | Acetaminophen | 50 in 1 BOTTLE | TABLET | 50 | 5 | |
| 69842-298-10 | Acetaminophen | 100 in 1 BOTTLE | TABLET | 100 | 5 | |
| 69842-298-15 | Acetaminophen | 150 in 1 BOTTLE | TABLET | 150 | 5 | |
| 69842-298-21 | Acetaminophen | 225 in 1 BOTTLE | TABLET | 225 | 5 | |
| 69842-298-24 | Acetaminophen | 24 in 1 BOTTLE | TABLET | 24 | 5 | |
| 69842-298-30 | Acetaminophen | 300 in 1 BOTTLE | TABLET | 300 | 5 | |
| 69842-298-40 | Acetaminophen | 400 in 1 BOTTLE | TABLET | 400 | 5 | |
| 69842-298-60 | Acetaminophen | 600 in 1 BOTTLE | TABLET | 600 | 5 |
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 |
|---|---|---|---|---|---|---|
| Dolex Children Pain and Fever | ACETAMINOPHEN | Pharmadel LLC | f9158463-aeb1-5de0-e053-6294a90a748b | 2024-03-04 | Warnings | M013 |
| SEDALMEX FORTE | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Belmora LLC | 33b3508e-4caa-4d05-9b15-cb82a2ee2d4d | 2024-02-28 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | AMERISOURCE BERGEN | 2b923a97-836c-4dac-a8c0-3047a35fb62e | 2024-02-23 | Warnings | M013 |
| Pain Reliever PM Extra Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | BJWC (Berkley & Jensen / BJ's) | b20a08f3-c9c0-4bd9-8ce0-acb932b5bb86 | 2024-02-22 | Warnings | M013 |
| M-PAP | ACETAMINOPHEN | Bryant Ranch Prepack | 31a41976-7f65-42d7-acf5-de9c2c5ca58e | 2024-02-20 | Warnings | M013 |
| Publix Fast Relief Effervescent - Original Flavor | ASPIRIN | PUBLIX SUPER MARKETS INC. | 0a342f72-45fd-3e12-e063-6394a90ae33e | 2024-02-16 | Warnings | M013 |
| Equaline Effervescent Pain Reliever | ASPIRIN | UNITED NATURAL FOODS, INC. DBA UNFI | 0761299a-e913-7665-e063-6394a90a6003 | 2024-02-16 | Warnings | M013 |
| TopCare Effervescent Pain Relief | ASPIRIN | TOPCO ASSOCIATES LLC | 075f36e1-110c-e839-e063-6294a90a89d7 | 2024-02-16 | Warnings | M013 |
| Extra Strength Pain Reliever | ACETAMINOPHEN | INGLES MARKETS, INC. | 115d0b4f-6f0f-79a9-e063-6394a90ab18a | 2024-02-14 | Warnings | M013 |
| PANADOL | ACETAMINOPHEN | Haleon US Holdings LLC | e1799765-c247-42b4-ad6a-8ba7d136abf2 | 2024-02-06 | Warnings | M013 |
| Panadol Cold and Flu NonDrowsy | ACETAMINOPHEN AND PHENYLEPRINE HCL | Haleon US Holdings LLC | f626ab17-01c9-4493-ba9e-0c8c11146384 | 2024-02-06 | Warnings | M013 |
| PANADOL Extra | ACETAMINOPHEN AND CAFFEINE | Haleon US Holdings LLC | e5c2d88a-d903-4ca0-b895-f27e791dfc4e | 2024-02-06 | Warnings | M013 |
| PANADOL Extra Strength | ACETAMINOPHEN | Haleon US Holdings LLC | b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b | 2024-02-06 | Warnings | M013 |
| PANADOL Extra Strength | ACETAMINOPHEN | Haleon US Holdings LLC | 9d384e88-5c11-4600-ac6c-a38371570138 | 2024-02-06 | Warnings | M013 |
| PANADOL | ACETAMINOPHEN | Haleon US Holdings LLC | 95801755-db54-4ad7-bec1-52671914f6ca | 2024-02-06 | Warnings | M013 |
| PANADOL PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HCL | Haleon US Holdings LLC | 01e7dddb-755c-4745-b701-edcdb6209064 | 2024-02-06 | Warnings, Adverse reactions | M013 |
| PANADOL PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HCL | Haleon US Holdings LLC | fe7cd1f2-9b00-4ded-99c2-8a152c71093c | 2024-02-06 | Warnings, Adverse reactions | M013 |
| Childrens Pain and Fever | ACETAMINOPHEN | AptaPharma Inc. | 9064943f-836f-4853-b6f2-2c4879941eeb | 2024-02-02 | Warnings | M013 |
| Quality Choice Effervescent Pain Relief | ASPIRIN | CHAIN DRUG MARKETING ASSOCIATION, INC. | 079af5d7-1be8-2a93-e063-6294a90a496d | 2024-02-01 | Warnings | M013 |
| MEDI-FIRST Non-Aspirin | ACETAMINOPHEN | Proficient Rx LP | 4c84948d-3a95-4c53-8529-7e7b9d8bb6df | 2024-02-01 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198440 | acetaminophen 500 MG Oral Tablet | PSN | 852e70e2-7279-6f33-e053-2991aa0a8676 | 5 |
| 198440 | acetaminophen 500 MG Oral Tablet | SCD | 852e70e2-7279-6f33-e053-2991aa0a8676 | 5 |
| 198440 | APAP 500 MG Oral Tablet | SY | 852e70e2-7279-6f33-e053-2991aa0a8676 | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69842-298-05 | 69842029805 | 50 TABLET in 1 BOTTLE (69842-298-05) | 50 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 69842-298-10 | 69842029810 | 100 TABLET in 1 BOTTLE (69842-298-10) | 100 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 69842-298-15 | 69842029815 | 150 TABLET in 1 BOTTLE (69842-298-15) | 150 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 69842-298-21 | 69842029821 | 225 TABLET in 1 BOTTLE (69842-298-21) | 225 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 69842-298-24 | 69842029824 | 24 TABLET in 1 BOTTLE (69842-298-24) | 24 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 69842-298-30 | 69842029830 | 300 TABLET in 1 BOTTLE (69842-298-30) | 300 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 69842-298-40 | 69842029840 | 400 TABLET in 1 BOTTLE (69842-298-40) | 400 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 69842-298-60 | 69842029860 | 600 TABLET in 1 BOTTLE (69842-298-60) | 600 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |