NDC 82725-4202-01 - Goodmeds Non Drowsy Allergy Relief
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
- 82725-4202
- Requested NDC
- 82725-4202-01
- Package NDCs from labels
- 82725-4202-1, 82725-4202-01
- Manufacturer
- Cabinet Health P.B.C.
- Effective date
- 2026-04-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Goodmeds Non Drowsy Allergy Relief | Cabinet Health P.B.C. | 2026-04-20 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82725-4202-1 | Goodmeds Non Drowsy Allergy Relief | 120 in 1 BOTTLE | TABLET | 120 | 1 |
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.
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| Fexofenadine | FEXOFENADINE | YYBA Corp | 579c7ff9-0c44-1d46-e063-6294a90aef34 | 2026-07-27 | Warnings | 2S068B75ZU |
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