UNDA 202
- Product NDC
- 62106-1176
- Requested package NDC
- 62106-1176-8
- 11-digit product format
- 621061176
- Labeler code
- 62106
- Product ID
- 62106-1176_c7335cbe-8359-b482-e053-2a95a90a24ac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aurum metallicum, Calcarea fluorica, Cuprum metallicum, Gelsemium sempervirens, Sulphur
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Seroyal USA
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-09-22
- Substance
- CALCIUM FLUORIDE; COPPER; GELSEMIUM SEMPERVIRENS WHOLE; SULFUR; GOLD
- Active strength
- 12; 12; 4; 6; 12 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Standardized Chemical Allergen [EPC]
- 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 202
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CALCIUM FLUORIDE | 12 [hp_X]/20mL |
| COPPER | 12 [hp_X]/20mL |
| GELSEMIUM SEMPERVIRENS WHOLE | 4 [hp_X]/20mL |
| SULFUR | 6 [hp_X]/20mL |
| GOLD | 12 [hp_X]/20mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 6D74QW4H67 | Internal UNII lookup |
| Q4EWM09M3O | Internal UNII lookup |
| O3B55K4YKI | Internal UNII lookup |
| R0519OZO3K | Internal UNII lookup |
| 79Y1949PYO | Internal UNII lookup |
| CLF5YFS11O | Internal UNII lookup |
| JWF5YAW3QW | Internal UNII lookup |
| 789U1901C5 | Internal UNII lookup |
| 70FD1KFU70 | Internal UNII lookup |
| Q21UUL2105 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 205b68ed-ff41-3559-e054-00144ff88e88 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c599c4a0-705d-4ebb-ab1f-977af038f96a | Product name | 1 | 20251124 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62106-1176-8 | UNDA 202 | 20 mL in 1 BOTTLE, GLASS | LIQUID | 20 | 6 | |
| 62106-1176-8 | UNDA 202 | 1 in 1 CARTON | LIQUID | 1 | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62106-1176 | UNDA 210 (BOLDO LEAF, CRATAEGUS, LACTUCA VIROSA, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS) LIQUID UNDA 202 (AURUM METALLICUM, CALCAREA FLUORICA, CUPRUM METALLICUM, GELSEMIUM SEMPERVIRENS, SULPHUR) LIQUID [SEROYAL USA] | 6 | Current NDC, Legacy NDC, 2 package rows | 20210717_205b68ed-ff41-3559-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 210 | BOLDO LEAF, CRATAEGUS, LACTUCA VIROSA, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS | Seroyal USA | 205b68ed-ff41-3559-e054-00144ff88e88 | 2021-07-15 | Warnings | 62106-1176-8 62106-1176 62106117608 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 62106-1176-8 | 62106117608 | 1 BOTTLE, GLASS in 1 CARTON (62106-1176-8) / 20 mL in 1 BOTTLE, GLASS | 2015-09-22 | 0000-00-00 | No | No | Current |