Aurum 21X

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2026-01-16
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:36:49

Label at a glance#

ProductAurum 21X

Active ingredientGOLD

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

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 Ingredient: Aurum metallicum (Metallic gold) 21X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt

Prepared using rhythmical processes.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
shopuriel.com

Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aurum 21X Ampule

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1318-1	Aurum 21X	10 in 1 BOX	LIQUID	10		3
48951-1318-1	Aurum 21X	1 mL in 1 AMPULE	LIQUID	1		3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Aurum 21X
GOLD
SODIUM CHLORIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-1318	48951-1318-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GOLD	79Y1949PYO	ACTIB
SODIUM CHLORIDE	451W47IQ8X	IACT
WATER	059QF0KO0R	IACT

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
Aurum 21X	AURUM 21X	Uriel Pharmacy Inc.	93f243c0-b963-9ea0-e053-2995a90aa852	2026-01-16	Warnings	Exact identifier ndc (package): 48951-1318-1 ndc (product): 48951-1318 ndc11 (package): 48951131801 spl id: 48889afd-554b-a47f-e063-6394a90a9bb0 spl set id: 93f243c0-b963-9ea0-e053-2995a90aa852

Reported adverse events (FAERS/openFDA)#

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