NDC 79481-0152-01 - DUAL ACTION BACK PAIN RELIEVER
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
- 79481-0152
- Requested NDC
- 79481-0152-01
- Package NDCs from labels
- 79481-0152-1, 79481-0152-0, 79481-0152-01
- Manufacturer
- Meijer, Inc.
- Effective date
- 2026-03-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Meijer Distribution, Inc. Dual Action Back Pain Reliever Drug Facts | Meijer, Inc. | 2026-03-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0152-0 | DUAL ACTION BACK PAIN RELIEVER | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 2 | |
| 79481-0152-1 | DUAL ACTION BACK PAIN RELIEVER | 72 in 1 BOTTLE | TABLET, FILM COATED | 72 | 2 |
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.