FDA.reportPublic FDA data

Echinacea Argentum

Manufacturer
Uriel Pharmacy Inc.
Effective date
2021-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:33

Label at a glance#

ProductEchinacea Argentum
Active ingredientECHINACEA, UNSPECIFIED, SILVER, ATROPA BELLADONNA, SILICON DIOXIDE
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 Ingredients: Echinacea e pl. tota (Purple coneflower) 3X, Atropa belladonna ex herba (Nightshade) 20X, Quartz (Rock crystal) 20X, Argentum met. (Silver) 30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, Sodium bicarbonate, Rose oil

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
www.urielpharmacy.com Lot#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Echinacea Argentum 10mlEchinacea Argentum 10mlEchinacea Argentum 10mlEchinacea Argentum 10ml

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
48951-4166-1Echinacea Argentum10 mL in 1 BOTTLE, DROPPERLIQUID101
48951-4166-1Echinacea Argentum1 in 1 BAGLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4166ECHINACEA ARGENTUM LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20210507_c1acc2cf-a819-60b3-e053-2a95a90a502e.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
48951-416648951-4166-1

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
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
SILVER3M4G523W1GACTIB
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
ROSE OILWUB68Y35M7IACT
SODIUM BICARBONATE8MDF5V39QOIACT
ATROPA BELLADONNAWQZ3G9PF0HACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB

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
c1acc2cf-a81a-60b3-e053-2a95a90a502ec1acc2cf-a819-60b3-e053-2a95a90a502e2021-05-06WarningsExact identifier
spl id: c1acc2cf-a81a-60b3-e053-2a95a90a502e
spl set id: c1acc2cf-a819-60b3-e053-2a95a90a502e

Reported adverse events (FAERS/openFDA)#

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