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 |
|---|---|---|---|---|---|---|
| Childrens Acetaminophen | ACETAMINOPHEN | Bryant Ranch Prepack | bdc466c9-d9ae-4293-b7ea-46fb517661c6 | 2025-04-01 | Warnings | M013 |
| Adult Low Dose Enteric Coated Aspirin | ASPIRIN | Geri-Care Pharmaceutical Corp | e327a52a-0e31-44b7-9823-7f60d070ae52 | 2025-04-01 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | Proficient Rx LP | 9af5ccc8-aac0-4339-a9f6-58fdc9b91c57 | 2025-04-01 | Warnings | M013 |
| ASPIRIN 325 MG EC | ASPIRIN | Bryant Ranch Prepack | 9d0449d2-c0c6-4e74-931b-35dc62584028 | 2025-03-31 | Warnings | M013 |
| Aspirin 81 mg | ASPIRIN | Bryant Ranch Prepack | cce1e8bd-63c8-403a-bc32-e6788493f604 | 2025-03-31 | Warnings | M013 |
| Adwe Feverx Acetaminophen Caplets, 500 mg Extra Strength | ACETAMINOPHEN | Aurex Laboratories Limited Liability Company | 948c5826-6f35-484d-bb3f-cecf6a4b5c13 | 2025-03-31 | Warnings | M013 |
| Infants Pain and Fever | ACETAMINOPHEN | WALGREENS | 281a530b-c759-50eb-e063-6394a90abb4f | 2025-03-28 | Warnings | M013 |
| Pain Reliever PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | WR Group, Inc. | 8281771c-485c-42a9-9a1c-9a7a4298c5b8 | 2025-03-28 | Warnings | M013 |
| Acetaminophen Regular strength | ACETAMINOPHEN | PD-Rx Pharmaceuticals, Inc. | 4181efc2-d183-410c-b647-233444c57e32 | 2025-03-20 | Warnings | M013 |
| CounterAct Pain | ACETAMINOPHEN | Melaleuca, Inc. | 7faf76b4-7f25-377d-e053-2a91aa0a19d4 | 2025-03-20 | Boxed warning, Warnings | M013 |
| Mejoral | ACETAMINOPHEN, CAFFEINE | OPMX LLC | 0bccf571-fcb9-2dd5-e063-6294a90a5f16 | 2025-03-19 | Warnings | M013 |
| ARTRIFIN 24 CAPLETS | ACETAMINOPHEN, ASPIRIN, CAFFEINE | OPMX LLC | e7f15c2b-a730-b54f-e053-2a95a90a3b3e | 2025-03-19 | Warnings | M013 |
| Pain Reliever PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | TARGET Corporation | 1fc3806e-a5c4-4a6e-951b-dfbf9f5771f1 | 2025-03-17 | Warnings | M013 |
| Signature Select Effervescent Pain Relief | ASPIRIN | Safeway Inc. | 304fca65-2867-c963-e063-6394a90a183f | 2025-03-14 | Warnings | M013 |
| GOOD REMEDIES Extra Strength Pain Relief PM Caplet | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | Strive Pharmaceuticals Inc. | 2d642d8e-c154-a970-e063-6294a90a03bf | 2025-03-14 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | DISCOUNT DRUG MART | 97f78c4a-9d0d-4fe1-8b2b-d5f8ab939ac4 | 2025-03-07 | Warnings | M013 |
| Redicare Non-Aspirin 500mg | REDICARE NON-ASPIRIN, ACETAMINOPHEN 500MG | Redicare LLC | 2f229898-1777-732c-e063-6394a90a76bc | 2025-03-04 | Warnings, Adverse reactions | M013 |
| Major Extra Strength Acetaminophen Liquid | ACETAMINOPHEN | Major Pharmaceuticals | 2f3af4dd-45d5-87b4-e063-6294a90ab3cc | 2025-02-28 | Warnings | M013 |
| LOW DOSE ASPIRIN | ASPIRIN | NCS HealthCare of KY, LLC dba Vangard Labs | ed9a71d6-a56e-416a-bb89-6d41307efc5a | 2025-02-27 | Warnings | M013 |
| Aspirin | ASPIRIN | PD-Rx Pharmaceuticals, Inc. | 77429b7f-78e4-42c0-8679-ae8da1748848 | 2025-02-26 | 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 |