NDC 43074-108-01 - Dyabetex
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
- 43074-108
- Requested NDC
- 43074-108-01
- Package NDCs from labels
- 43074-108-01, 43074-108-02
- Manufacturer
- Phillips Company
- Effective date
- 2010-09-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dyabetex - Phillips Company | Phillips Company | 2010-09-05 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43074-108-02 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-cad7-621f-e053-dbdaa90a74ad | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43074-108-01 | Dyabetex | 3 mL in 1 BOTTLE, DROPPER | OINTMENT | 3 | 1 | |
| 43074-108-02 | Dyabetex | 1 in 1 BOTTLE, PLASTIC | OINTMENT | 1 | 1 |
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.