NDC 84269-2550-02 - Back Pain Relief Extra Strength Doans
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
- 84269-2550
- Requested NDC
- 84269-2550-02
- Package NDCs from labels
- 84269-2550-2, 84269-2550-02
- Manufacturer
- Wildman Business Group | LNK International, Inc. | Medique Products | Prestige Packaging
- Effective date
- 2024-07-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Magnesium Salicylate - Wildman Business Group | LNK International, Inc. | Medique Products | Prestige Packaging | Wildman Business Group | LNK International, Inc. | Medique Products | Prestige Packaging | 2024-07-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84269-2550-2 | Back Pain Relief Extra Strength Doans | 2 in 1 PACKET | TABLET, FILM COATED | 2 | 1 | |
| 84269-2550-2 | Back Pain Relief Extra Strength Doans | 50 in 1 BOX | TABLET, FILM COATED | 50 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 84269-2550 | BACK PAIN RELIEF EXTRA STRENGTH DOANS (MAGNESIUM SALICYLATE) TABLET, FILM COATED [WILDMAN BUSINESS GROUP] | 1 | Current NDC, 2 package rows | 20240701_2e17664f-a83f-48d1-8b2b-37f41eea65b6.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.