Argentum 10/20/30

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2024-12-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:29:26

Label at a glance#

ProductArgentum 10/20/30

Active ingredientSILVER

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Argentum met. (Silver) 10X/20X/30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt

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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Argentum 10 20 30 Ampules

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1383-1	Argentum 10/20/30	1 mL in 1 AMPULE	LIQUID	1		1
48951-1383-1	Argentum 10/20/30	10 in 1 BOX	LIQUID	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1383	ARGENTUM 10/20/30 LIQUID [URIEL PHARMACY INC.]	1	2 package rows	20241212_28ec4cd6-2d6c-2325-e063-6294a90aa7ab.zip

Products#

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

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

Argentum 10/20/30
WATER
SODIUM CHLORIDE
SILVER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-1383	48951-1383-1

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
WATER	059QF0KO0R	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
SILVER	3M4G523W1G	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
28ec6f6e-aac1-88b2-e063-6394a90a36b1			28ec4cd6-2d6c-2325-e063-6294a90aa7ab	2024-12-09	Warnings	Exact identifier spl id: 28ec6f6e-aac1-88b2-e063-6394a90a36b1 spl set id: 28ec4cd6-2d6c-2325-e063-6294a90aa7ab

Reported adverse events (FAERS/openFDA)#

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