Secale Argentum
- Manufacturer
- Uriel Pharmacy Inc. | Uriel Pharmacy, Inc.
- Effective date
- 2021-08-03
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:14:47
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Directions: FOR ORAL USE ONLY.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Aristolochia (Common birthwort) 3X, Pulsatilla (Pasqueflower) 6X, Secale corn. e grano (Ergot) 6X, Argentum met. (Silver) 8X
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Organic sucrose
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. 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
www.urielpharmacy.com Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-8383-2 | Secale Argentum | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-8383 | SECALE ARGENTUM PELLET [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20210811_c8be6955-2641-0e9a-e053-2995a90a9a27.zip |
Products#
Every source-derived product name is available through these pages.
- Secale Argentum
- PULSATILLA VULGARIS
- ARISTOLOCHIA CLEMATITIS WHOLE
- CLAVICEPS PURPUREA SCLEROTIUM
- SUCROSE
- SILVER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-8383 | 48951-8383-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PULSATILLA VULGARIS | I76KB35JEV | ACTIB |
| ARISTOLOCHIA CLEMATITIS WHOLE | T47L342B3C | ACTIB |
| CLAVICEPS PURPUREA SCLEROTIUM | 01G9XEA93N | ACTIB |
| SUCROSE | C151H8M554 | IACT |
| SILVER | 3M4G523W1G | 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 |
|---|---|---|---|---|---|---|
| c8be6955-2642-0e9a-e053-2995a90a9a27 | c8be6955-2641-0e9a-e053-2995a90a9a27 | 2021-08-03 | Warnings | c8be6955-2642-0e9a-e053-2995a90a9a27 c8be6955-2641-0e9a-e053-2995a90a9a27 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
