Onopordon Aurum

Manufacturer: Uriel Pharmacy, Inc.
Effective date: 2024-11-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:28:57

Label at a glance#

ProductOnopordon Aurum

Active ingredientHYOSCYAMUS NIGER LEAF, GOLD, ONOPORDUM ACANTHIUM FLOWER, PRIMULA VERIS FLOWER

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

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: 100gm contains: 2.5gm Onopordon (Cotton thistle) 1X, 2.5gm Primula (Cowslip) 1X; Hyoscyamus (Henbane) 3X, Aurum met. (Metallic gold) 10X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 30% Organic cane alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Promotes healthy circulatory support.

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

Onopordon Aurum Liquid

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-7210-3	2026-01-29	C162847	48780-1	49896155-a7ef-586f-e063-e6dba90add90	Onopordon Aurum

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7210-3	Onopordon Aurum	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-7210	ONOPORDON AURUM LIQUID [URIEL PHARMACY, INC.]	1	1 package rows	20241120_2737024d-1a48-a7f7-e063-6294a90a50cc.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Onopordon Aurum
HYOSCYAMUS NIGER LEAF
GOLD
ONOPORDUM ACANTHIUM FLOWER
ALCOHOL
WATER
PRIMULA VERIS FLOWER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-7210	48951-7210-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HYOSCYAMUS NIGER LEAF	32IT7G8BAW	ACTIB
GOLD	79Y1949PYO	ACTIB
ONOPORDUM ACANTHIUM FLOWER	AP97AUF88E	ACTIB
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
PRIMULA VERIS FLOWER	W5BET37294	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2737024d-1a49-a7f7-e063-6294a90a50cc			2737024d-1a48-a7f7-e063-6294a90a50cc	2024-11-18	Warnings	Exact identifier spl id: 2737024d-1a49-a7f7-e063-6294a90a50cc spl set id: 2737024d-1a48-a7f7-e063-6294a90a50cc

Reported adverse events (FAERS/openFDA)#

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