NDC 86100-0002 - Kidney/Bladder
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
- 86100-0002
- Package NDCs from labels
- 86100-0002-1
- Manufacturer
- Vsf2, Inc. | Apotheca Company
- Effective date
- 2025-11-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Kidney/Bladder - Vsf2, Inc. | Apotheca Company | Vsf2, Inc. | Apotheca Company | 2025-11-10 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86100-0002-1 | Kidney/Bladder | 59 mL in 1 BOTTLE, SPRAY | LIQUID | 59 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86100-0002 | KIDNEY/BLADDER (APIS MELLIFICA, CALCAREA OXALICA, CANTHARIS, EQUISETUM HYEMALE, FERRUM PHOSPHORICUM, MAGNESIA PHOSPHORICA, PICRICUM ACIDUM, SEPIA) LIQUID [VSF2, INC.] | 1 | 1 package rows | 20190201_f2979ea5-acbd-402c-9ed8-0f8a4a213b43.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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.