FDA.reportPublic FDA data

Echinacea Quartz

Manufacturer
Uriel Pharmacy, Inc.
Effective date
2024-11-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:01

Label at a glance#

ProductEchinacea Quartz
Active ingredientANTIMONY TRISULFIDE, SILVER, SILICON DIOXIDE, ECHINACEA, UNSPECIFIED, ATROPA BELLADONNA
Label structure9 sections

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: Echinacea (Purple coneflower) 3X, Antimonite (Nat. antimony trisulfide) 6X, Argentum nitricum (Silver nitrate) 20X, Atropa belladonna (Nightshade) 20X, Quartz (Rock crystal) 20X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Rose oil, Lactose

Prepared using rhythmical processes

OTC - PURPOSE SECTION

Uses: Temporarily relieves pain of sensitive teeth, soreness in mouth or gum inflammation.

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. Contains traces of lactose. 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

Echinacea Quartz LiquidEchinacea Quartz Liquid

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4020-3Echinacea Quartz60 mL in 1 BOTTLE, DROPPERLIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4020ECHINACEA QUARTZ LIQUID [URIEL PHARMACY, INC.]21 package rows20241123_1170a19a-57e1-9c7d-e063-6294a90a1705.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-402048951-4020-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANTIMONY TRISULFIDEF79059A38UACTIB
WATER059QF0KO0RIACT
ROSE OILWUB68Y35M7IACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
ALCOHOL3K9958V90MIACT
SILVER3M4G523W1GACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB

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
278475b6-bed8-33e5-e063-6394a90a91701170a19a-57e1-9c7d-e063-6294a90a17052024-11-22WarningsExact identifier
spl id: 278475b6-bed8-33e5-e063-6394a90a9170
spl set id: 1170a19a-57e1-9c7d-e063-6294a90a1705

Reported adverse events (FAERS/openFDA)#

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