Acetaminophen
- Product NDC
- 50090-5313
- 11-digit product format
- 500905313
- Labeler code
- 50090
- Product ID
- 50090-5313_91673a66-2b9e-47ee-bb4b-61ec914a6226
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-09-12
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 50090-5313 | 50090-5313-5 | D | Discontinued by firm | 2026-10-21 |
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 | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 50090-5313 | 50090-5313-5 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 50090-5313 | 50090-5313-5 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
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 |
|---|---|
| 061c91d5-5aa8-4556-a344-197b7e8a10b8 | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-5313-1 | Acetaminophen | 30 in 1 BOTTLE | TABLET | 30 | 9 | |
| 50090-5313-2 | Acetaminophen | 100 in 1 BOTTLE | TABLET | 100 | 9 | |
| 50090-5313-3 | Acetaminophen | 50 in 1 BOTTLE | TABLET | 50 | 9 | |
| 50090-5313-4 | Acetaminophen | 24 in 1 BOTTLE | TABLET | 24 | 9 | |
| 50090-5313-5 | Acetaminophen | 20 in 1 BOTTLE | TABLET | 20 | 9 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-5313-1 | EA - Each | 50090-5313 | effbf6d1-2eef-4221-b574-d6134a638819 | 1 | 2023-02-06 |
| 50090-5313-2 | EA - Each | 50090-5313 | 53d0f9fb-68ea-435e-b087-968398d6e1a8 | 1 | 2023-02-06 |
| 50090-5313-3 | EA - Each | 50090-5313 | e524e326-e685-4569-9895-15bae917aa8a | 1 | 2023-02-06 |
| 50090-5313-4 | EA - Each | 50090-5313 | bd5a9d37-7123-4205-88dd-ffea425e28e6 | 1 | 2023-02-06 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-5313 | ACETAMINOPHEN TABLET [A-S MEDICATION SOLUTIONS] | 9 | Current NDC, Legacy NDC, 5 package rows | 20250502_061c91d5-5aa8-4556-a344-197b7e8a10b8.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 |
|---|---|---|---|---|---|---|
| Bayer Genuine Aspirin | BAYER GENUINE ASPIRIN | Lil' Drug Store Products, Inc. | d17834d7-cb3e-6bf2-e053-2a95a90ae5c1 | 2024-12-30 | Warnings | M013 |
| Extra Strength Pain Reliever | ACETAMINOPHEN 500 MG, FILM-COATED CAPLET | Lil' Drug Store Products, Inc. | e5fd2b46-683e-4cf5-e053-2995a90a5512 | 2024-12-30 | Warnings | M013 |
| Night Time Severe Cold and Cough Relief | ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL | Chain Drug Consortium, LLC | c8e9b57b-83e9-46c5-9791-02c4c2b94004 | 2024-12-29 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 1608b4f0-bf20-4024-b8f2-20a4df7a4b21 | 2024-12-26 | Warnings | M013 |
| Aspirin | ASPIRIN | Advance Pharmaceutical Inc. | f6a9ea44-08b8-4a33-bfbd-68cb2d852c39 | 2024-12-26 | Warnings | M013 |
| ACETAMINOPHEN | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION INC | cfc7eac3-35be-4002-b8ef-be1dfc8caf69 | 2024-12-26 | Warnings | M013 |
| ACETAMINOPHEN | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION INC | a3031139-4709-43f2-95a8-89840c595f7f | 2024-12-26 | Warnings | M013 |
| Acetaminophen 250mg Aspirin 250mg Caffeine 65mg | ACETAMINOPHEN 250MG ASPIRIN 250MG CAFFEINE 65MG | WALGREENS CO. | 98bb28ed-d146-ca3d-e053-2a95a90a9eaf | 2024-12-26 | Warnings | M013 |
| Acetaminophen 500mg Caffeine 60mg Pyrilamine maleate 15mg | ACETAMINOPHEN 500MG CAFFEINE 60MG PYRILAMINE MALEATE 15MG | WALGREENS CO. | 982faa74-d498-cd1e-e053-2995a90afa1e | 2024-12-25 | Warnings | M013 |
| Childrens Pain and Fever | ACETAMINOPHEN | AptaPharma Inc. | 11bf6e1b-aed9-4f8f-9f03-ea911ae9f702 | 2024-12-23 | Warnings | M013 |
| Rugby Regular Strength Acetaminophen | ACETAMINOPHEN | RUGBY LABORATORIES | 295b0d00-4d4a-405f-9325-d01c5d4f3ed4 | 2024-12-20 | Warnings | M013 |
| Walgreens Pain Relief Powder | ASPIRIN AND CAFFEINE | Walgreens Co. | 61493d34-2432-4683-9b32-e1851a4337be | 2024-12-18 | Warnings | M013 |
| Reese Headache Powders | ASPIRIN AND CAFFEINE | Reese Pharmaceutical Co | 386f7a6c-4bfc-4140-a67b-07f6b520d58f | 2024-12-18 | Warnings | M013 |
| NobleAid PAIN RELIEVER | ASPIRIN | Noble Otc LLC | aa08e488-2f69-4d7e-86ba-ccfad563edcf | 2024-12-18 | Warnings | M013 |
| Dollar General Headache Powders | ASPIRIN AND CAFFEINE | Dolgencorp, LLC | 11b0271b-d65c-49c4-a081-d71044a0e04c | 2024-12-18 | Warnings | M013 |
| Family Wellness Pain Relief Powder | ASPIRIN AND CAFFEINE | Family Dollar Services Inc | b2e55de7-3c36-49cc-8f7f-1013fd1ec359 | 2024-12-18 | Warnings | M013 |
| Best Choice Pain Relief Powder | ASPIRIN AND CAFFEINE | Value Merch | a95b9b22-ea5c-4a02-b35d-c8ae1e117604 | 2024-12-18 | Warnings | M013 |
| Walmart Pain Relief Powder | ASPIRIN AND CAFFEINE | Walmart | c69aa61f-6a74-40a3-8737-195fa545e261 | 2024-12-18 | Warnings | M013 |
| Quality Choice Pain Relief Powder | ASPIRIN AND CAFFEINE | Chain Drug Marketing Association | 8e1f4057-4968-4523-9b3f-55aea421b674 | 2024-12-18 | Warnings | M013 |
| Equaline Effervescent Antacid and Pain Relief | ASPIRIN, CITRIC ACID, SODIUM BICARBONATE | United Natural Foods, Inc. dba UNFI | 739237a5-cc62-8ad6-e053-2991aa0a91f8 | 2024-12-17 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198440 | acetaminophen 500 MG Oral Tablet | PSN | 061c91d5-5aa8-4556-a344-197b7e8a10b8 | 9 |
| 198440 | acetaminophen 500 MG Oral Tablet | SCD | 061c91d5-5aa8-4556-a344-197b7e8a10b8 | 9 |
| 198440 | APAP 500 MG Oral Tablet | SY | 061c91d5-5aa8-4556-a344-197b7e8a10b8 | 9 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50090-5313-1 | 50090531301 | 30 TABLET in 1 BOTTLE (50090-5313-1) | 30 tablet | 2020-10-29 | 0000-00-00 | No | No | Current |
| 50090-5313-2 | 50090531302 | 100 TABLET in 1 BOTTLE (50090-5313-2) | 100 tablet | 2020-10-29 | 0000-00-00 | No | No | Current |
| 50090-5313-3 | 50090531303 | 50 TABLET in 1 BOTTLE (50090-5313-3) | 50 tablet | 2020-10-29 | 0000-00-00 | No | No | Current |
| 50090-5313-4 | 50090531304 | 24 TABLET in 1 BOTTLE (50090-5313-4) | 24 tablet | 2020-10-29 | 0000-00-00 | No | No | Current |
| 50090-5313-5 | 50090531305 | 20 TABLET in 1 BOTTLE (50090-5313-5) | 20 tablet | 2020-10-29 | 0000-00-00 | No | No | Current |