Argentum Veratrum
- 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 02:29:42
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Taraxacum (Dandelion) 2X, Urtica dioica (Stinging nettle) 2X, Cuprum sulf. (Copper sulfate) 4X, Magnesium sulf. (Magnesium sulfate) 4X, Apis (Honeybee) 5X, Apis regina (Queen Bee cell with larva and nutrient fluid) 5X, Pancreas (Bovine pancreas) 5X, Saccharum Sacchari (Cane sugar) 5X, Veratrum (White hellebore) 5X, Argentum met. (Silver) 6X, Phosphorus (Yellow phosphorus) 6X, Gl. Parathyreoidea (Bovine parathyroid glands) 8X, Aurum met. (Metallic gold) 9X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Organic sucrose, Lactose
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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1358-2 | Argentum Veratrum | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-1358 | ARGENTUM VERATRUM PELLET [URIEL PHARMACY, INC.] | 2 | Legacy NDC, 1 package rows | 20241219_eac58c77-dbf5-c9ee-e053-2a95a90a70e1.zip |
Products#
Every source-derived product name is available through these pages.
- Argentum Veratrum
- PHOSPHORUS
- APIS MELLIFERA
- BOS TAURUS PARATHYROID GLAND
- TARAXACUM PALUSTRE ROOT
- SUCROSE
- LACTOSE, UNSPECIFIED FORM
- SILVER
- GOLD
- CUPRIC SULFATE
- CUPRIC CATION
- SUS SCROFA PANCREAS
- SUGARCANE
- URTICA DIOICA
- MAGNESIUM SULFATE, UNSPECIFIED
- MAGNESIUM CATION
- ROYAL JELLY
- VERATRUM ALBUM ROOT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1358 | 48951-1358-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PHOSPHORUS | 27YLU75U4W | ACTIB |
| APIS MELLIFERA | 7S82P3R43Z | ACTIB |
| BOS TAURUS PARATHYROID GLAND | SMV71DDI4T | ACTIB |
| TARAXACUM PALUSTRE ROOT | GCZ4W7077C | ACTIB |
| SUCROSE | C151H8M554 | IACT |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| SILVER | 3M4G523W1G | ACTIB |
| GOLD | 79Y1949PYO | ACTIB |
| CUPRIC SULFATE | LRX7AJ16DT | ACTIM |
| SUS SCROFA PANCREAS | 9Y3J3362RY | ACTIB |
| SUGARCANE | 81H2R5AOH3 | ACTIB |
| URTICA DIOICA | 710FLW4U46 | ACTIB |
| MAGNESIUM SULFATE, UNSPECIFIED | DE08037SAB | ACTIB |
| ROYAL JELLY | L497I37F0C | ACTIB |
| VERATRUM ALBUM ROOT | QNS6W5US1Z | 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 |
|---|---|---|---|---|---|---|
| 297ba2df-b0fa-6efb-e063-6394a90a96ea | eac58c77-dbf5-c9ee-e053-2a95a90a70e1 | 2024-12-17 | Warnings | 297ba2df-b0fa-6efb-e063-6394a90a96ea eac58c77-dbf5-c9ee-e053-2a95a90a70e1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
