NDC 87239-1111-01 - Lidoxi
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
- 87239-1111
- Requested NDC
- 87239-1111-01
- Package NDCs from labels
- 87239-1111-1, 87239-1111-01
- Manufacturer
- T&T Pharma Holdings LLC
- Effective date
- 2026-05-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lidoxi - T&T Pharma Holdings LLC | T&T Pharma Holdings LLC | 2026-05-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87239-1111-1 | Lidoxi | 92 g in 1 TUBE, WITH APPLICATOR | OINTMENT | 92 | 1 |
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.