UNDA 29
- Product NDC
- 62106-1128
- 11-digit product format
- 621061128
- Labeler code
- 62106
- Product ID
- 62106-1128_ed107ed6-cf0a-1d5a-e053-2a95a90af33b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Absinthium, Allium cepa, Argentum metallicum, Betula pendula Sap, Lamium album, Salvia officinalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Seroyal USA
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-09-21
- Substance
- LAMIUM ALBUM; WORMWOOD; ONION; SILVER; BETULA PENDULA WOOD; SAGE
- Active strength
- 4; 4; 4; 12; 4; 4 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- UNDA 29
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| LAMIUM ALBUM | 4 [hp_X]/20mL |
| WORMWOOD | 4 [hp_X]/20mL |
| ONION | 4 [hp_X]/20mL |
| SILVER | 12 [hp_X]/20mL |
| BETULA PENDULA WOOD | 4 [hp_X]/20mL |
| SAGE | 4 [hp_X]/20mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 568ZVX88G6 | Internal UNII lookup |
| 2H1576D5WG | Internal UNII lookup |
| 7D3VB244UX | Internal UNII lookup |
| 046Y1357I6 | Internal UNII lookup |
| CPD4NFA903 | Internal UNII lookup |
| E55SMD6DA8 | Internal UNII lookup |
| JWF5YAW3QW | Internal UNII lookup |
| 3M4G523W1G | Internal UNII lookup |
| 492225Q21H | Internal UNII lookup |
| F84709P2XV | Internal UNII lookup |
| 065C5D077J | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 20484d33-4389-1a85-e054-00144ff88e88 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62106-1128-8 | UNDA 29 | 1 in 1 CARTON | LIQUID | 1 | 6 | |
| 62106-1128-8 | UNDA 29 | 20 mL in 1 BOTTLE, GLASS | LIQUID | 20 | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62106-1128 | UNDA 29 (ABSINTHIUM, ALLIUM CEPA, ARGENTUM METALLICUM, BETULA PENDULA SAP, LAMIUM ALBUM, SALVIA OFFICINALIS) LIQUID UNDA 38 (ALUMINIUM METALLICUM, ARGENTUM METALLICUM, INULA HELENIUM, SARSAPARILLA, STIGMATA MAIDIS, VALERIANA OFFICINALIS) LIQUID [SEROYAL USA] | 6 | Current NDC, Legacy NDC, 2 package rows | 20221110_20484d33-4389-1a85-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 29 | ABSINTHIUM, ALLIUM CEPA, ARGENTUM METALLICUM, BETULA PENDULA SAP, LAMIUM ALBUM, SALVIA OFFICINALIS | Seroyal USA | 20484d33-4389-1a85-e054-00144ff88e88 | 2022-11-09 | Warnings | 62106-1128 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 62106-1128-8 | 62106112808 | 1 BOTTLE, GLASS in 1 CARTON (62106-1128-8) / 20 mL in 1 BOTTLE, GLASS | 2015-09-21 | 0000-00-00 | No | No | Current |