NDC 62106-1124-08 - UNDA 25
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
- 62106-1124
- Requested NDC
- 62106-1124-08
- Package NDCs from labels
- 62106-1124-8, 62106-1124-08
- Manufacturer
- Seroyal USA | SAN’UP
- Effective date
- 2021-07-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| UNDA 25 - Seroyal USA | SAN’UP | Seroyal USA | SAN’UP | 2021-07-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62106-1124-8 | UNDA 25 | 1 in 1 CARTON | LIQUID | 1 | 6 | |
| 62106-1124-8 | UNDA 25 | 20 mL in 1 BOTTLE, GLASS | LIQUID | 20 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62106-1124 | UNDA 25 (ARGENTUM METALLICUM, CRATAEGUS, GELSEMIUM SEMPERVIRENS, HAMAMELIS VIRGINIANA, MAGNOLIA GRANDIFLORA, SPIRAEA ULMARIA, STANNUM METALLICUM, VALERIANA OFFICINALIS) LIQUID UNDA 27 (ANTIMONIUM CRUDUM, BORAGO OFFICINALIS, CETRARIA ISLANDICA, DROSERA, MENTHA PIPERITA, SENEGA OFFICINALIS) LIQUID UNDA 22 (ABSINTHIUM, ACONITUM NAPELLUS, ARGENTUM METALLICUM, BOLDO LEAF, CHAMOMILLA, COFFEA TOSTA, JATEORHIZA PALMATA, MANGANUM OXYDATUM NIGRUM, SALVIA OFFICINALIS) LIQUID UNDA 12 (ARGENTUM METALLICUM, AURUM METALLICUM, DULCAMARA, FAGOPYRUM ESCULENTUM, ILLICIUM VERUM, LAPPA MAJOR, SALVIA OFFICINALIS, SARSAPARILLA, STAPHYSAGRIA, VIOLA TRICOLOR) LIQUID [SEROYAL USA] | 6 | Current NDC, Legacy NDC, 2 package rows | 20210717_2044a04e-275f-3f16-e054-00144ff8d46c.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.