Pain Reliever
- Product NDC
- 49035-984
- 11-digit product format
- 490350984
- Labeler code
- 49035
- Product ID
- 49035-984_9a7210b1-ce6f-49a4-988b-03043f1ad630
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Wal-Mart Stores Inc
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-17
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 49035-984-10 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 49035-984-10 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 49035-984-10 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 49035-984-10 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 49035-984-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 49035-984-10 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 49035-984-10 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 49035-984-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded product | product | ad56d346431e… | cc804d4bbf1e… | |
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded package | package | 49035-984-10 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded product | product | 367a005e9d99… | 383a685ebd0f… | |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded package | package | 49035-984-10 | 367a005e9d99… | 383a685ebd0f… |
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
- Pain Reliever
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49035-984-10 | Pain Reliever | 40 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 40 | 5 | |
| 49035-984-10 | Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 5 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49035-984-10 | EA - Each | 49035-984 | 48d5f17e-f160-4783-a3c9-e4c41bea3963 | 1 | 2023-04-07 |
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 |
|---|---|---|---|---|---|---|
| INFANTS PAIN AND FEVER | ACETAMINOPHEN | Amazon.com Services LLC | 112076c4-cac2-45ab-9c77-5573edae7180 | 2026-07-10 | Warnings | M013 |
| Aspirin | ASPIRIN | Wal-Mart Stores Inc | 8ae16aa2-54bc-4c1a-aa36-93524199a67b | 2026-07-09 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | Wildman Business Group | 943c8f49-e65e-40bc-b364-3274df4d21a2 | 2026-07-09 | Warnings | M013 |
| Aspirin Regular Strength | ASPIRIN | FOODHOLD U.S.A., LLC | 9e09b4fb-e015-45ea-8b1c-27faf65572aa | 2026-07-09 | Warnings | M013 |
| Tension Headache Relief | ACETAMINOPHEN, CAFFEINE | Walgreen Company | f13fb7e9-50ea-4e2c-a442-38b1b5b315d7 | 2026-07-09 | Warnings | M013 |
| Acetaminophen 500 Pyrilamine Maleate 15 and Caffeine 60 | ACETAMINOPHEN 500MG PYRILAMINE MALEATE 15MG AND CAFFEINE 60MG TABLETS | Health Pharma USA LLC | 34eb8a9b-d0ee-13e8-e063-6294a90a2fef | 2026-07-08 | Warnings | M013 |
| Acetaminophen 250 mg Aspirin 250 mg Caffeine 65 mg | ACETAMINOPHEN 250 MG ASPIRIN 250 MG CAFFEINE 65 MG | Health Pharma USA LLC | 3590d417-272b-ae4d-e063-6394a90a5dc6 | 2026-07-08 | Warnings | M013 |
| GOODMEDS EXTRA STRENGTH PAIN RELIEF ACETAMINOPHEN | ACETAMINOPHEN | Cabinet Health P.B.C. | 88884253-5a79-4ac1-b8ce-03966d8b509d | 2026-07-08 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | Health Pharma USA LLC | 671adabe-5f82-4599-a133-3f67ccb34079 | 2026-07-07 | Warnings | M013 |
| Pain Reliever Plus | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Rugby Laboratories | c3df1652-96a8-6043-e053-2995a90a2d26 | 2026-07-07 | Warnings | M013 |
| Rapidol Aspirin | ASPIRIN | Pharmadel LLC | 00d9ab0d-ff25-784f-e063-6294a90a8497 | 2026-07-06 | Warnings | M013 |
| Aspirin | ASPIRIN | Trifecta Pharmaceuticals USA LLC | 227cefca-acc4-41d0-e063-6394a90a35b9 | 2026-07-06 | Warnings | M013 |
| Extra Strength Pain Aid | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Hi-Tech Nutaceuticals, LLC | a39e4b99-700d-0f5c-e053-2a95a90a6bd3 | 2026-07-06 | Warnings | M013 |
| Nighttime Sleep Aid | ACETAMINOPHEN, DIPHENHYDRAMINE | Hi-Tech Nutraceuticals, LLC | a39e2bd6-3d0a-642b-e053-2995a90a42a0 | 2026-07-06 | Warnings | M013 |
| Extra Strength Acetaminophen | ACETAMINOPHEN | Hi-Tech Nutraceuticals, LLC | a36be487-7a36-550f-e053-2a95a90a95c1 | 2026-07-06 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | Hi-Tech Nutraceuticals, LLC | a39c524e-c131-d7fb-e053-2995a90a785b | 2026-07-06 | Warnings | M013 |
| PAIN RELIEVER | ASPIRIN 81 MG | Health Pharma USA, LLC | d60aed37-3a9e-46d1-e053-2995a90a1d1f | 2026-07-06 | Warnings | M013 |
| Tylenol PM Extra Strength | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | Select Consumer Group | 55d0dceb-c9a9-778e-e063-6294a90a2ad7 | 2026-07-04 | Warnings | M013 |
| Bayer Genuine Aspirin | ASPIRIN | Select Consumer Group | 3ca776c2-47ed-5107-e063-6394a90ac5df | 2026-07-03 | Warnings | M013 |
| Aspirin | ASPIRIN | Rugby Laboratories | f7ca9f4a-f8ef-46d2-9536-b69541e6653d | 2026-07-02 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198440 | acetaminophen 500 MG Oral Tablet | PSN | a856ed05-206b-4169-9809-6ea9cad43f5b | 5 |
| 198440 | acetaminophen 500 MG Oral Tablet | SCD | a856ed05-206b-4169-9809-6ea9cad43f5b | 5 |
| 198440 | APAP 500 MG Oral Tablet | SY | a856ed05-206b-4169-9809-6ea9cad43f5b | 5 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 49035-984-10 | 49035098410 | 1 BOTTLE, PLASTIC in 1 CARTON (49035-984-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2019-04-17 | 0000-00-00 | No | No | Current |