FDA.reportPublic FDA data

Strophanthus Aurum

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:44

Label at a glance#

ProductStrophanthus Aurum
Active ingredientONOPORDUM ACANTHIUM FLOWER, PRIMULA VERIS FLOWER, HYOSCYAMUS NIGER LEAF, STROPHANTHUS KOMBE WHOLE, 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: Onopordon (Cotton thistle) 3X, Primula (Cowslip) 3X, Hyoscyamus (Henbane) 4X, Strophanthus (Strophantus) 5X, Stibium met. (Antimony) 8X, Aurum met. (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 Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Strophanthus Aurum LiquidStrophanthus Aurum Liquid

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8403-3Strophanthus Aurum60 mL in 1 BOTTLE, DROPPERLIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8403STROPHANTHUS AURUM LIQUID [URIEL PHARMACY INC.]21 package rows20241222_0ac18643-77b3-ace9-e063-6394a90a9c82.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-840348951-8403-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
ONOPORDUM ACANTHIUM FLOWERAP97AUF88EACTIB
PRIMULA VERIS FLOWERW5BET37294ACTIB
HYOSCYAMUS NIGER LEAF32IT7G8BAWACTIB
STROPHANTHUS KOMBE WHOLEQ1O0N901S4ACTIB
ANTIMONY9IT35J3UV3ACTIB
GOLD79Y1949PYOACTIB

Source Document#

Source XML

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
29a1c46a-e4ab-01ce-e063-6294a90a34790ac18643-77b3-ace9-e063-6394a90a9c822024-12-19WarningsExact identifier
spl id: 29a1c46a-e4ab-01ce-e063-6294a90a3479
spl set id: 0ac18643-77b3-ace9-e063-6394a90a9c82

Reported adverse events (FAERS/openFDA)#

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