Aurum Hypericum Stibium
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2022-05-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:17:23
Label at a glance#
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: Aurum met. (Metallic gold) 10X, Hypericum (St. Johns wort) 10X, Stibium met. (Antimony) 10X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt
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
Made by 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 |
|---|---|---|---|---|---|---|
| 48951-1340-1 | Aurum Hypericum Stibium | 10 in 1 BOX | LIQUID | 10 | 2 | |
| 48951-1340-1 | Aurum Hypericum Stibium | 1 mL in 1 AMPULE | LIQUID | 1 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-1340 | AURUM HYPERICUM STIBIUM LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 2 package rows | 20220507_b6c26f9a-4ff1-11c6-e053-2995a90a4887.zip |
Products#
Every source-derived product name is available through these pages.
- Aurum Hypericum Stibium
- ANTIMONY
- SODIUM CHLORIDE
- WATER
- GOLD
- ST. JOHN'S WORT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1340 | 48951-1340-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ANTIMONY | 9IT35J3UV3 | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| WATER | 059QF0KO0R | IACT |
| GOLD | 79Y1949PYO | ACTIB |
| ST. JOHN'S WORT | UFH8805FKA | 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 |
|---|---|---|---|---|---|---|
| de5d3f29-19b4-379b-e053-2a95a90a0ae8 | b6c26f9a-4ff1-11c6-e053-2995a90a4887 | 2022-05-06 | Warnings | de5d3f29-19b4-379b-e053-2a95a90a0ae8 b6c26f9a-4ff1-11c6-e053-2995a90a4887 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
