NDC 43857-0249-01 - Diathesis I
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
- 43857-0249
- Requested NDC
- 43857-0249-01
- Package NDCs from labels
- 43857-0249-1, 43857-0249-01
- Manufacturer
- BioActive Nutritionals, Inc. | Apotheca Company
- Effective date
- 2018-07-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diathesis I - BioActive Nutritionals, Inc. | Apotheca Company | BioActive Nutritionals, Inc. | Apotheca Company | 2018-07-13 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43857-0249-1 | DiathesisI | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43857-0249 | DIATHESIS I (MANGANUM METALLICUM, GERMANIUM SESQUIOXIDE, FEL TAURI, HEPAR SUIS, GINKGO BILOBA, CYSTEINUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, ARSENICUM ALBUM, FUMARICUM ACIDUM, PHOSPHORUS, SODIUM OXALATE, SULPHUR) LIQUID [BIOACTIVE NUTRITIONALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20180714_e8c3b763-7d54-48b1-8db8-a5b47ce7aeeb.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.