NDC 43074-207-01 - VenomX
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
- 43074-207
- Requested NDC
- 43074-207-01
- Package NDCs from labels
- 43074-207-01, 43074-207-02
- Manufacturer
- Phillips Company
- Effective date
- 2010-09-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| VenomX - Phillips Company | Phillips Company | 2010-09-04 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43074-207-02 | 2019-11-13 | C162847 | 48780-1 | 97449f38-c533-f6ea-e053-dbdaa90aa703 | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43074-207-01 | VenomX | 3 mL in 1 BOTTLE, DROPPER | LIQUID | 3 | 13 | |
| 43074-207-02 | VenomX | 1 in 1 BOTTLE, PLASTIC | LIQUID | 1 | 13 |
DailyMed Dashboard NDC Coverage#
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.