NDC 43857-0217-01 - Enuresis
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
- 43857-0217
- Requested NDC
- 43857-0217-01
- Package NDCs from labels
- 43857-0217-1, 43857-0217-01
- Manufacturer
- BioActive Nutritional, Inc. | Apotheca Company
- Effective date
- 2017-06-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Enuresis - BioActive Nutritional, Inc. | Apotheca Company | BioActive Nutritional, Inc. | Apotheca Company | 2017-06-14 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43857-0217-1 | Enuresis | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43857-0217 | ENURESIS (EQUISETUM HYEMALE, SOLIDAGO VIRGAUREA, UVA-URSI, ARGENTUM METALLICUM, CAUSTICUM, KREOSOTUM, NITRICUM ACIDUM, SEPIA, THUJA OCCIDENTALIS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20170615_22105dde-b570-4af6-a7b8-e942f649e934.zip |
DailyMed Socrata Ingredients#
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.