Helleborus comp. E
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2024-12-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:29:41
Label at a glance#
ProductHelleborus comp. E
Active ingredientHELLEBORUS NIGER ROOT, ANTIMONY, KALANCHOE DAIGREMONTIANA LEAF, HELLEBORUS FOETIDUS ROOT, ROSMARINUS OFFICINALIS FLOWERING TOP, LEAD, CHINESE YAM, GOLD
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE.
DOSAGE & ADMINISTRATION SECTION
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Bryophyllum (Life plant) 2X, Dioscorea batata (Chinese yam) 3X, Rosmarinus (Rosemary) 8X, Aurum (Metallic gold) 12X, Helleborus e pl. tota (Christmas rose) 12X, Plumbum mellitum (Lead with honey) 20X, Helleborus e fol. (Christmas rose) 21X, Stibium (Antimony) 30X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Use: Temporary relief of headache.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
WARNINGS SECTION
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-5121-1 | Helleborus comp. E | 1 mL in 1 AMPULE | LIQUID | 1 | 2 | |
| 48951-5121-1 | Helleborus comp. E | 10 in 1 BOX | LIQUID | 10 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-5121 | HELLEBORUS COMP. E LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 2 package rows | 20241219_97df45bd-27e7-2fc1-e053-2a95a90a8792.zip |
Products#
Every source-derived product name is available through these pages.
- Helleborus comp. E
- HELLEBORUS NIGER ROOT
- ANTIMONY
- SODIUM CHLORIDE
- KALANCHOE DAIGREMONTIANA LEAF
- HELLEBORUS FOETIDUS ROOT
- ROSMARINUS OFFICINALIS FLOWERING TOP
- LEAD
- CHINESE YAM
- WATER
- GOLD
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-5121 | 48951-5121-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HELLEBORUS NIGER ROOT | 608DGJ6815 | ACTIB |
| ANTIMONY | 9IT35J3UV3 | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| KALANCHOE DAIGREMONTIANA LEAF | L6X13JKL8O | ACTIB |
| HELLEBORUS FOETIDUS ROOT | 332Y7EES96 | ACTIB |
| ROSMARINUS OFFICINALIS FLOWERING TOP | 8JM482TI79 | ACTIB |
| LEAD | 2P299V784P | ACTIB |
| CHINESE YAM | 29CIF30B1Z | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GOLD | 79Y1949PYO | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 297b303e-102b-3f2e-e063-6294a90ad85f | 97df45bd-27e7-2fc1-e053-2a95a90a8792 | 2024-12-17 | Warnings | 297b303e-102b-3f2e-e063-6294a90ad85f 97df45bd-27e7-2fc1-e053-2a95a90a8792 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.