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#

ProductAurum Stibium Hyoscyamus
Active ingredientHYOSCYAMUS NIGER LEAF, ANTIMONY, GOLD
Label structure9 sections

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

Aurum Stibium Hyoscyamus LiquidAurum Stibium Hyoscyamus Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1403-3Aurum Stibium Hyoscyamus60 in 1 BOTTLE, DROPPERLIQUID608

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANTIMONYACTIVE INGREDIENT9IT35J3UV31
GOLDACTIVE INGREDIENT79Y1949PYO1
HYOSCYAMUS NIGER LEAFACTIVE INGREDIENT32IT7G8BAW1
ONOPORDUM ACANTHIUM FLOWERACTIVE INGREDIENTAP97AUF88E1
PRIMULA VERIS FLOWERACTIVE INGREDIENTW5BET372941
ANTIMONYACTIVE MOIETY9IT35J3UV31
GOLDACTIVE MOIETY79Y1949PYO1
HYOSCYAMUS NIGER LEAFACTIVE MOIETY32IT7G8BAW1
ONOPORDUM ACANTHIUM FLOWERACTIVE MOIETYAP97AUF88E1
PRIMULA VERIS FLOWERACTIVE MOIETYW5BET372941
SUCROSEINACTIVE INGREDIENTC151H8M5541
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-140348951-1403-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SUCROSESUCROSEC151H8M554LIQUID / ORAL37500 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
SUCROSESUCROSEC151H8M554LIQUID / ORAL37500 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Aurum Stibium HyoscyamusAURUM STIBIUM HYOSCYAMUSURIEL PHARMACY INC.29ca80e6-3797-4ca2-a9cc-ea384b38ba5b2025-09-02WarningsExact identifier
ndc (package): 48951-1403-3
ndc (product): 48951-1403
ndc11 (package): 48951140303
spl id: 3dd77cd3-4f85-c9b2-e063-6294a90adc7c
spl set id: 29ca80e6-3797-4ca2-a9cc-ea384b38ba5b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.