Pain Relief Aspirin
- Product NDC
- 11822-2180
- 11-digit product format
- 118222180
- Labeler code
- 11822
- Product ID
- 11822-2180_bf297166-0b88-4929-ab29-76fcf0b1ae6b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1990-09-12
- Marketing end
- 0000-00-00
- Substance
- ASPIRIN
- Active strength
- 81 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 product | product | 11822-2180 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 11822-2180 | 11822-2180-7 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 11822-2180 | 11822-2180-9 | 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 | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 11822-2180-9 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 11822-2180-7 | d630ba8d3edf… | 732f749b63fb… |
| 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 | 11822-2180-9 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 11822-2180-7 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 11822-2180-7 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 11822-2180-7 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 11822-2180-7 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 11822-2180-7 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 11822-2180-7 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 11822-2180-7 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 11822-2180-7 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded package | package | 11822-2180-7 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded package | package | 11822-2180-7 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | excluded package | package | 11822-2180-7 | 557ba5c1ecfa… | 9c80585c8c6e… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ASPIRIN | ACTIVE INGREDIENT | R16CO5Y76E | PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID] | 11 | |
| ASPIRIN | ACTIVE MOIETY | R16CO5Y76E | PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID] | 11 | |
| DEXTRATES | INACTIVE INGREDIENT | G263MI44RU | PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID] | 11 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID] | 11 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID] | 11 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11822-2180 | PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, CHEWABLE [RITE AID CORPORATION] | 24 | Legacy NDC | 20250312_77cfa372-e3ad-4112-bbd1-5227342aaafd.zip |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 11822-2180-9 | 11822218009 | 3 BOTTLE, PLASTIC in 1 CARTON (11822-2180-9) > 36 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC | 1990-09-12 | 0000-00-00 | No | No | Current |