Aurum Stibium
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2026-01-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:36:49
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Use: Temporary relief of headache.
INDICATIONS & USAGE SECTION
FOR ORAL USE ONLY
DOSAGE & ADMINISTRATION SECTION
Directions: Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Follow inside instructions to open ampule.
WARNINGS SECTION
Warnings:
NOT FOR INJECTION
Do not use if allergic to any ingredient. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Stibium met. (Antimony) 8X, Aurum met. (Metallic gold) 10X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt
Prepard using rhythmical processes.
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 |
|---|---|---|---|---|---|---|
| 48951-1346-1 | Aurum Stibium | 1 mL in 1 AMPULE | LIQUID | 1 | 2 | |
| 48951-1346-1 | Aurum Stibium | 10 in 1 BOX | LIQUID | 10 | 2 |
Products#
Every source-derived product name is available through these pages.
- Aurum Stibium
- SODIUM CHLORIDE
- ANTIMONY
- WATER
- GOLD
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1346 | 48951-1346-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| ANTIMONY | 9IT35J3UV3 | 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 |
|---|---|---|---|---|---|---|
| Aurum Stibium | AURUM STIBIUM | Uriel Pharmacy Inc. | bd35c88f-c646-4136-e053-2a95a90a0cc1 | 2026-01-16 | Warnings | 48951-1346-1 48951-1346 48951134601 48871cbc-a3b4-388c-e063-6394a90a3013 bd35c88f-c646-4136-e053-2a95a90a0cc1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
