All Day Pain Relief
- Product NDC
- 79903-005
- 11-digit product format
- 799030005
- Labeler code
- 79903
- Product ID
- 79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- WALMART INC.
- Application
- ANDA204872
- Marketing category
- ANDA
- Marketing start
- 2020-10-22
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- 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 | 79903-005 | 79903-005-10 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 79903-005 | 79903-005-12 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 79903-005 | 79903-005-30 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 79903-005 | 79903-005-75 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 79903-005 | 79903-005-99 | D | Discontinued by firm | 2026-10-05 |
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 | 79903-005 | 79903-005-75 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 79903-005 | 79903-005-75 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A204872-001 | NAPROXEN SODIUM | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 |
Observed Orange Book product history#
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 84e616aacf4f… | ||
| 2026-08-18 06:07:40 | 2026-07 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | caaa826d4ba7… | ||
| 2026-02-19 14:30 UTC | 2026-02 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 011fe1cb6892… | ||
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 31067a03dcf5… | ||
| 2025-08-23 18:47 UTC | 2025-08 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 6a471c1ec25d… | ||
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | fd3edfee7708… | ||
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | b8a1b40f171c… | ||
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 03ed91905a0d… | ||
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 2680178bc6a6… | ||
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 5bbf6a4d5a75… | ||
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | d8e5a09893c0… | ||
| 2024-10-29 15:01 UTC | 2024-10 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | d06236e962d9… | ||
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 79d66fd596c7… | ||
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 301d65b070ca… | ||
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 1e350fbaab3a… | ||
| 2024-05-31 18:47 UTC | 2024-05 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 8072bd15b7f6… | ||
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 5c6f7cd8ea54… | ||
| 2022-04-08 23:34 UTC | 2022-04 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 5d02ea3f76ae… | ||
| 2022-04-04 05:41 UTC | 2022-04 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 4b0b4de00fa7… | ||
| 2019-12-13 00:20 UTC | 2019-12 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 74a2ff9319b5… | ||
| 2022-03-09 01:35 UTC | 2022-03 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | bb7c543d1eb4… | ||
| 2021-12-28 21:50 UTC | 2021-12 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 782e0a99824c… | ||
| 2021-05-05 16:15 UTC · 3 captures of this ZIP | 2021-05 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 87673890dc5c… | ||
| 2021-03-12 10:30 UTC | 2021-03 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 5aa47cf7b7d7… | ||
| 2020-12-22 03:56 UTC | 2020-12 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 8869cabd3fbd… | ||
| 2020-11-12 02:37 UTC | 2020-11 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | c0c555d07b60… | ||
| 2019-12-14 00:12 UTC | 2019-12 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 3f01610625f2… | ||
| 2019-09-15 20:21 UTC | 2019-09 | A204872-001 | NAPROXEN SODIUM | EQ 200MG BASE | TABLET / ORAL | 2017-01-23 | b00525d2431f… | ||
| 2019-07-19 19:46 UTC | 2019-07 | A204872-001 | NAPROXEN SODIUM | EQ 200MG BASE | TABLET / ORAL | 2017-01-23 | ea99ee380514… | ||
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 6a51e52b5d6a… | ||
| 2024-02-18 07:12 UTC | 2024-02 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 1c564ffb4f44… | ||
| 2023-12-20 04:57 UTC | 2023-12 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | ea1830bbd6c7… | ||
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | a72a2bbeb626… | ||
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 9b2671bbb829… | ||
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | a67488948f0b… | ||
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 3f0d92c62455… | ||
| 2023-05-13 08:27 UTC | 2023-05 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 053a50430f4f… | ||
| 2023-01-26 05:58 UTC | 2023-01 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 3bdfa0b2c4d7… | ||
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | 3a93d1ddd44b… | ||
| 2022-10-28 04:53 UTC | 2022-10 | A204872-001 | NAPROXEN SODIUM | 220MG | TABLET / ORAL | 2017-01-23 | f41ea6bd6efb… |
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
- All Day Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| NAPROXEN SODIUM | 220 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9TN87S3A3C | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 849574 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| c4909e43-57ba-44bc-a234-a02cc884891c | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fef6ad89-235f-4274-ba49-a8e53642473e | Product name | 2 | 20250225 |
| 87fed3e6-8fba-48ef-96b0-3a7fb54b96ff | Product name | 3 | 20230306 |
| b5fdaaec-7251-4da6-9cb2-4e9e76939ec8 | Product name | 1 | 20200623 |
| e76dbbc1-775d-722c-08ff-ed45e8a80def | Product name | 3 | 20181002 |
| 6f4f4521-fd56-1ae6-888b-3b021bd75c7c | Product name | 1 | 20140508 |
| ce67e27d-1d21-5465-4409-b0662dd99d4d | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79903-005-10 | All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 13 | |
| 79903-005-10 | All Day Pain Relief | 40 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 40 | 13 | |
| 79903-005-12 | All Day Pain Relief | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 13 | |
| 79903-005-20 | All Day Pain Relief | 200 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 200 | 13 | |
| 79903-005-25 | All Day Pain Relief | 225 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 225 | 13 | |
| 79903-005-27 | All Day Pain Relief | 270 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 270 | 13 | |
| 79903-005-30 | All Day Pain Relief | 300 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 300 | 13 | |
| 79903-005-75 | All Day Pain Relief | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 13 | |
| 79903-005-75 | All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 13 | |
| 79903-005-90 | All Day Pain Relief | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | 13 | |
| 79903-005-99 | All Day Pain Relief | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 13 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 79903-005-10 | EA - Each | 79903-005 | 0630f354-453e-4269-9f6c-ac94167769b3 | 1 | 2023-08-08 |
| 79903-005-12 | EA - Each | 79903-005 | bbd701e0-2c8e-45be-b28c-fb69a3d4766b | 1 | 2025-07-08 |
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 |
|---|---|---|---|---|---|---|
| Naproxen | NAPROXEN SODIUM | Family Dollar Services Inc | b6205032-f5c6-494a-8b87-adbbbc3982e7 | 2025-10-27 | Warnings | 204872 ANDA204872 |
| Naproxen | NAPROXEN SODIUM | Amerisource Bergen | 1e2e6e3a-b095-4d5b-86fe-61eb44a87cf0 | 2025-10-20 | Warnings | 204872 ANDA204872 |
| First Aid Direct All Day Pain Relief | NAPROXEN SODIUM | Cintas Corporation | 1c9384c1-52f8-4482-88fc-5f5b6d770c42 | 2025-09-22 | Warnings | 204872 ANDA204872 |
| Naproxen | NAPROXEN SODIUM | Geri-Care Pharmaceutical Corp | 9a61d544-e46d-6703-e053-2a95a90a32fd | 2025-02-27 | Warnings | 204872 ANDA204872 |
| Naproxen | NAPROXEN SODIUM | NuCare Pharmaceuticals,Inc. | f1ed8384-83d6-6f2a-e053-2a95a90ab08f | 2025-02-04 | Warnings | 204872 ANDA204872 |
| Naproxen | NAPROXEN SODIUM | Bryant Ranch Prepack | f9ddc614-26b7-48dc-ae93-02da6388f2d5 | 2025-01-30 | Warnings | 204872 ANDA204872 |
| Naproxen | NAPROXEN SODIUM | Proficient Rx LP | 2acd8e24-449d-4f5c-9323-504013ff4bf5 | 2023-07-28 | Warnings | 204872 ANDA204872 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 849574 | naproxen sodium 220 MG Oral Tablet | PSN | c4909e43-57ba-44bc-a234-a02cc884891c | 13 |
| 849574 | naproxen sodium 220 MG Oral Tablet | SCD | c4909e43-57ba-44bc-a234-a02cc884891c | 13 |
| 849574 | naproxen sodium 220 MG (as naproxen 200 MG) Oral Tablet | SY | c4909e43-57ba-44bc-a234-a02cc884891c | 13 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 79903-005-10 | 79903000510 | 1 BOTTLE, PLASTIC in 1 CARTON (79903-005-10) > 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2020-10-22 | 0000-00-00 | No | No | Current |
| 79903-005-12 | 79903000512 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-12) | 2020-10-22 | 0000-00-00 | No | No | Current |
| 79903-005-20 | 79903000520 | 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20) | 2020-10-22 | No | No | Current | |
| 79903-005-25 | 79903000525 | 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25) | 2020-10-22 | No | No | Current | |
| 79903-005-27 | 79903000527 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27) | 2020-10-22 | No | No | Current | |
| 79903-005-30 | 79903000530 | 300 in 1 BOTTLE, PLASTIC | Historical | ||||
| 79903-005-75 | 79903000575 | 1 BOTTLE, PLASTIC in 1 CARTON (79903-005-75) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2020-10-22 | 0000-00-00 | No | No | Current |
| 79903-005-90 | 79903000590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90) | 2020-10-22 | No | No | Current | |
| 79903-005-99 | 79903000599 | 100 in 1 BOTTLE, PLASTIC | Historical |