NDC 68466-2001-08 - Triflora Gel
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
- 68466-2001
- Requested NDC
- 68466-2001-08
- Package NDCs from labels
- 68466-2001-8, 68466-2001-4, 68466-2001-08
- Manufacturer
- Schwabe Mexico S.A. de C.V.
- Effective date
- 2025-11-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Triflora Gel | Schwabe Mexico S.A. de C.V. | 2025-11-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68466-2001-4 | Triflora Gel | 1 in 1 CARTON | GEL | 1 | 5 | |
| 68466-2001-4 | Triflora Gel | 28 g in 1 TUBE | GEL | 28 | 5 | |
| 68466-2001-8 | Triflora Gel | 1 in 1 CARTON | GEL | 1 | 5 | |
| 68466-2001-8 | Triflora Gel | 77 g in 1 TUBE | GEL | 77 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68466-2001 | TRIFLORA GEL (URTICA DIOICA, TOXICODENDRON PUBESCENS LEAF, LEDUM PALUSTRE TWIG) GEL [SCHWABE MEXICO S.A. DE C.V.] | 4 | Current NDC, Legacy NDC, 4 package rows | 20241215_a1c113ad-8c6c-4f19-b611-426e30f1db0e.zip |
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.