NDC 11822-4130-02 - pain relief back and body EXTRA STRENGTH
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 11822-4130
- Requested NDC
- 11822-4130-02
- Package NDCs from labels
- 11822-4130-2, 11822-4130-5, 11822-4130-02
- Manufacturer
- Rite Aid Corporation | LNK International, Inc.
- Effective date
- 2026-01-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rite Aid 44-413 | Rite Aid Corporation | LNK International, Inc. | 2026-01-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11822-4130-2 | pain relief back and bodyEXTRA STRENGTH | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 9 | |
| 11822-4130-2 | pain relief back and bodyEXTRA STRENGTH | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 9 | |
| 11822-4130-5 | pain relief back and bodyEXTRA STRENGTH | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | 9 | |
| 11822-4130-5 | pain relief back and bodyEXTRA STRENGTH | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11822-4130 | PAIN RELIEF BACK AND BODY EXTRA STRENGTH (ASPIRIN, CAFFEINE) TABLET, FILM COATED [RITE AID CORPORATION] | 8 | Current NDC, Legacy NDC, 4 package rows | 20250110_a71392c8-3f5b-4d00-baba-a4055ed68bc1.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.