Aurum Stibium Hyoscyamus
- Manufacturer
- URIEL PHARMACY INC.
- Effective date
- 2025-09-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- full-release
- Hydrated at
- 2026-06-01 02:34:56
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Hyoscyamus (Henbane) 4X, Stibium metallicum (Antimony) 8X, Aurum metallicum (Metallic gold) 10X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, 20% Organic cane alcohol
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. Do not use if safety seal is broken or missing.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1403-3 | Aurum Stibium Hyoscyamus | 60 in 1 BOTTLE, DROPPER | LIQUID | 60 | 8 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ANTIMONY | ACTIVE INGREDIENT | 9IT35J3UV3 | 1 | |
| GOLD | ACTIVE INGREDIENT | 79Y1949PYO | 1 | |
| HYOSCYAMUS NIGER LEAF | ACTIVE INGREDIENT | 32IT7G8BAW | 1 | |
| ONOPORDUM ACANTHIUM FLOWER | ACTIVE INGREDIENT | AP97AUF88E | 1 | |
| PRIMULA VERIS FLOWER | ACTIVE INGREDIENT | W5BET37294 | 1 | |
| ANTIMONY | ACTIVE MOIETY | 9IT35J3UV3 | 1 | |
| GOLD | ACTIVE MOIETY | 79Y1949PYO | 1 | |
| HYOSCYAMUS NIGER LEAF | ACTIVE MOIETY | 32IT7G8BAW | 1 | |
| ONOPORDUM ACANTHIUM FLOWER | ACTIVE MOIETY | AP97AUF88E | 1 | |
| PRIMULA VERIS FLOWER | ACTIVE MOIETY | W5BET37294 | 1 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- Aurum Stibium Hyoscyamus
- WATER
- SUCROSE
- HYOSCYAMUS NIGER LEAF
- ANTIMONY
- GOLD
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1403 | 48951-1403-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| SUCROSE | C151H8M554 | IACT |
| HYOSCYAMUS NIGER LEAF | 32IT7G8BAW | ACTIB |
| ANTIMONY | 9IT35J3UV3 | ACTIB |
| GOLD | 79Y1949PYO | ACTIB |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| SUCROSE | SUCROSE | C151H8M554 | LIQUID / ORAL | 37500 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | LIQUID / ORAL | 37500 mg |
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 Hyoscyamus | AURUM STIBIUM HYOSCYAMUS | URIEL PHARMACY INC. | 29ca80e6-3797-4ca2-a9cc-ea384b38ba5b | 2025-09-02 | Warnings | 48951-1403-3 48951-1403 48951140303 3dd77cd3-4f85-c9b2-e063-6294a90adc7c 29ca80e6-3797-4ca2-a9cc-ea384b38ba5b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
