NDC 86147-040 - KIDNEY DRAINER
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
- 86147-040
- Package NDCs from labels
- 86147-040-01
- Manufacturer
- Groupe Cyrenne Inc.
- Effective date
- 2025-11-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| KIDNEY DRAINER - Groupe Cyrenne Inc. | Groupe Cyrenne Inc. | 2025-11-20 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86147-040-01 | KIDNEY DRAINER | 30 mL in 1 BOTTLE | LIQUID | 30 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86147-040 | KIDNEY DRAINER (SILVER, ASPARAGUS, BERBERIS VULGARIS ROOT BARK, GENISTA TINCTORIA WHOLE, JUNIPER BERRY, PETROSELINUM CRISPUM WHOLE, FRANGULA ALNUS BARK, CAPSELLA BURSA-PASTORIS WHOLE, SOLIDAGO VIRGAUREA FLOWERING TOP) LIQUID [GROUPE CYRENNE INC.] | 4 | 1 package rows | 20241206_83fcdd2b-40b8-40d3-b059-5dd725843b4b.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.