FDA.reportPublic FDA data

Argentum Nitricum 4X

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-04-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:33

Label at a glance#

ProductArgentum Nitricum 4X
Active ingredientSILVER
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

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 Ingredient: Argentum nitricum (Silver nitrate) 4X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Potassium nitrate, Sodium bicarbonate, Rose oil

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.

REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.
Opened on:_________________

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Argentum nitricum 4 10mL LiquidArgentum nitricum 4 10mL LiquidArgentum nitricum 4 LiquidArgentum nitricum 4 Liquid

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1317-1Argentum Nitricum 4X10 mL in 1 BOTTLE, DROPPERLIQUID102
48951-1317-1Argentum Nitricum 4X1 in 1 BAGLIQUID12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1317ARGENTUM NITRICUM 4X LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20240403_8afcd2a3-38d6-2f96-e053-2995a90afc06.zip

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
48951-131748951-1317-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SILVER3M4G523W1GACTIB
WATER059QF0KO0RIACT
POTASSIUM NITRATERU45X2JN0ZIACT
SODIUM BICARBONATE8MDF5V39QOIACT
ROSE OILWUB68Y35M7IACT

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
1521ce1f-dd4d-b5b8-e063-6394a90a49818afcd2a3-38d6-2f96-e053-2995a90afc062024-04-02WarningsExact identifier
spl id: 1521ce1f-dd4d-b5b8-e063-6394a90a4981
spl set id: 8afcd2a3-38d6-2f96-e053-2995a90afc06

Reported adverse events (FAERS/openFDA)#

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