UNDA 10
- Product NDC
- 62106-1109
- 11-digit product format
- 621061109
- Labeler code
- 62106
- Product ID
- 62106-1109_ecfa1477-78a8-d93d-e053-2995a90af9b8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Absinthium, Argentum metallicum, Equisetum arvense, Juniperus communis, Millefolium, Rhamnus frangula
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Seroyal USA
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-09-29
- Substance
- ACHILLEA MILLEFOLIUM; EQUISETUM ARVENSE BRANCH; FRANGULA ALNUS BARK; JUNIPER BERRY; SILVER; WORMWOOD
- Active strength
- 4; 4; 4; 4; 12; 4 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- UNDA 10
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SILVER | 4 [hp_X]/20mL |
| EQUISETUM ARVENSE BRANCH | 4 [hp_X]/20mL |
| JUNIPER BERRY | 4 [hp_X]/20mL |
| WORMWOOD | 4 [hp_X]/20mL |
| ACHILLEA MILLEFOLIUM | 12 [hp_X]/20mL |
| FRANGULA ALNUS BARK | 4 [hp_X]/20mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 97C5T2UQ7J | Internal UNII lookup |
| Q4EWM09M3O | Internal UNII lookup |
| 8502S3Z5N1 | Internal UNII lookup |
| 2S713A4VP3 | Internal UNII lookup |
| O84B5194RL | Internal UNII lookup |
| 3M4G523W1G | Internal UNII lookup |
| F84709P2XV | Internal UNII lookup |
| 2FXJ6SW4PK | Internal UNII lookup |
| 1L0VKZ185E | Internal UNII lookup |
| S2D77IH61R | Internal UNII lookup |
| C88X29Y479 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 20ea57db-ad94-2c1c-e054-00144ff88e88 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62106-1109-8 | UNDA 10 | 1 in 1 CARTON | LIQUID | 1 | 7 | |
| 62106-1109-8 | UNDA 10 | 20 mL in 1 BOTTLE, GLASS | LIQUID | 20 | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62106-1109 | UNDA 10 (ABSINTHIUM, ARGENTUM METALLICUM, EQUISETUM ARVENSE, JUNIPERUS COMMUNIS, MILLEFOLIUM, RHAMNUS FRANGULA) LIQUID UNDA 243 (BOLDO LEAF, CHOLESTERINUM, COMBRETUM MICRANTHUM, LYCOPODIUM CLAVATUM, PODOPHYLLUM PELTATUM) LIQUID [SEROYAL USA] | 7 | Current NDC, Legacy NDC, 2 package rows | 20221109_20ea57db-ad94-2c1c-e054-00144ff88e88.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| UNDA 10 | ABSINTHIUM, ARGENTUM METALLICUM, EQUISETUM ARVENSE, JUNIPERUS COMMUNIS, MILLEFOLIUM, RHAMNUS FRANGULA | Seroyal USA | 20ea57db-ad94-2c1c-e054-00144ff88e88 | 2022-11-08 | Warnings | 62106-1109 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 62106-1109-8 | 62106110908 | 1 BOTTLE, GLASS in 1 CARTON (62106-1109-8) / 20 mL in 1 BOTTLE, GLASS | 2015-09-29 | 0000-00-00 | No | No | Current |