Regular Strength Pain Relief
- Product NDC
- 57896-102
- 11-digit product format
- 578960102
- Labeler code
- 57896
- Product ID
- 57896-102_2a93e117-2d7d-3bdd-e063-6294a90a4f28
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Geri-Care Pharmaceutical Corp
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1989-01-01
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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
- Regular Strength Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 313782 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 6158e954-32d8-4718-e053-2a91aa0a27f3 | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57896-102-01 | Regular Strength Pain Relief | 100 in 1 BOTTLE | TABLET | 100 | 8 | |
| 57896-102-05 | Regular Strength Pain Relief | 50 in 1 BOTTLE | TABLET | 50 | 8 | |
| 57896-102-10 | Regular Strength Pain Relief | 1000 in 1 BOTTLE | TABLET | 1000 | 8 | |
| 57896-102-20 | Regular Strength Pain Relief | 200 in 1 BOTTLE | TABLET | 200 | 8 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 57896-102-01 | EA - Each | 57896-102 | 4fd0e2b7-fd19-4784-9e24-f0fc69b74910 | 1 | 2019-01-24 |
| 57896-102-05 | EA - Each | 57896-102 | b63010e7-a608-44c2-b043-44d6f2818c59 | 1 | 2019-02-13 |
| 57896-102-10 | EA - Each | 57896-102 | 6b3d573d-baa1-4daf-aba9-717aa1dcfc74 | 1 | 2019-02-13 |
| 57896-102-20 | EA - Each | 57896-102 | 40b6eab0-c1a1-4c63-82f8-78251de158a2 | 1 | 2021-12-08 |
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 |
|---|---|---|---|---|---|---|
| Acetaminophen Diphenhydramine HCL | ACETAMINOPHEN DIPHENHYDRAMINE HCL | WALGREENS CO. | d92d97a8-0ee3-1206-e053-2a95a90a72a8 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | SAM'S WEST INC | 0c8e7095-0806-4501-e063-6394a90a89aa | 2025-12-19 | Warnings | M013 |
| Acetaminophen Diphenhydramine HCL | ACETAMINOPHEN DIPHENHYDRAMINE HCL | WALGREEN CO. | b3763182-2428-155a-e053-2995a90ab578 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | WALGREENS | e467b78e-9f23-5563-e053-2a95a90a586e | 2025-12-19 | Warnings | M013 |
| Acetaminophen Diphenhydramine HCL | ACETAMINOPHEN DIPHENHYDRAMINE HCL | Walgreens | fd7c3250-35d4-494a-e053-6394a90a2db5 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | CVS PHARMACY, INC | 1ddb8a2b-3081-3eda-e063-6294a90ab82b | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | CVS PHARMACY, INC | b1307d52-10e6-46e1-e053-2995a90a03b6 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | CVS PHARMACY, INC | c2c6d6a1-b492-506d-e053-2995a90aac23 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | FAMILY DOLLAR | f8383108-0970-9f1e-e053-6294a90ad38f | 2025-12-19 | Warnings | M013 |
| ACETAMINOPHEN 500 MG | ACETAMINOPHEN | NUVICARE LLC | 591ee107-e953-4982-b75f-13a0afd7c4ae | 2025-12-19 | Warnings | M013 |
| Nuvicare Headache Relief | ACETAMINOPHEN, ASPIRIN, CAFFEINE | NUVICARE LLC | 3ede0fb6-c089-4253-9878-2b01c39e9c87 | 2025-12-19 | Warnings | M013 |
| Aspirin Low Dose | ASPIRIN | NUVICARE LLC | 3a4aa3c7-b726-4303-8803-74196fa5637a | 2025-12-19 | Warnings | M013 |
| ACETAMINOPHEN 500 MG | ACETAMINOPHEN | NUVICARE LLC | 95edf7bd-b6a7-4be5-9ad7-8748e7c2d06e | 2025-12-19 | Warnings | M013 |
| Pain Relief PM | ACETAMINOPHEN, DIPHENHYDRAMINE | NUVICARE LLC | 32a5611b-9bf6-4850-a7ff-fa240da04f45 | 2025-12-19 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | BETTER LIVING BRANDS LLC. | ac0e96d0-746e-fb42-e053-2a95a90a1957 | 2025-12-18 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | BETTER LIVING BRANDS LLC. | ac0e5dc0-96eb-47b2-e053-2995a90add0e | 2025-12-18 | Warnings | M013 |
| Acetaminophen Diphenhydramine HCl | ACETAMINOPHEN DIPHENHYDRAMINE HCL | BETTER LIVING BRANDS LLC. | ac0f8d5c-d200-1156-e053-2a95a90aece6 | 2025-12-18 | Warnings | M013 |
| Pain and Fever Childrens | ACETAMINOPHEN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | e55645ab-66f9-4160-8247-395bc5b02711 | 2025-12-18 | Warnings | M013 |
| Dolex Forte | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Pharmadel LLC | 3c2d90fc-130d-476c-e063-6294a90a8c15 | 2025-12-17 | Warnings | M013 |
| CareOne Childrens Acetaminophen | ACETAMINOPHEN | American Sales Company | 07bc6632-fabb-427d-81f3-c27c54caa6a0 | 2025-12-17 | Warnings | M013 |
DailyMed RxNorm Mappings#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 57896-102-01 | 57896010201 | 100 TABLET in 1 BOTTLE (57896-102-01) | 100 tablet | 2011-12-01 | 0000-00-00 | No | No | Current |
| 57896-102-05 | 57896010205 | 50 TABLET in 1 BOTTLE (57896-102-05) | 50 tablet | 2011-12-01 | 0000-00-00 | No | No | Current |
| 57896-102-10 | 57896010210 | 1000 TABLET in 1 BOTTLE (57896-102-10) | 1000 tablet | 2012-01-01 | 0000-00-00 | No | No | Current |
| 57896-102-20 | 57896010220 | 200 TABLET in 1 BOTTLE (57896-102-20) | 200 tablet | 2018-07-01 | 0000-00-00 | No | No | Current |