FDA.reportPublic FDA data

Cinnabar Dandelion

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:29:45

Label at a glance#

ProductCinnabar Dandelion
Active ingredientELYMUS REPENS ROOT, TARAXACUM PALUSTRE ROOT, FERROUS CATION, CARBONATE ION, MERCURIC CATION
Label structure9 sections

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: Agropyron (Couch grass) 3X, Taraxacum (Dandelion) 3X, Pyrite (Nat. Iron disulfide) 8X, Kali carb e cinere Fagi (Potassium carbonate from beech wood ash) 10X, Cinnabaris (Nat. mercuric sulfide) 20X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporary relief of cold, flu and sore throat symptoms.

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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cinnabar Dandelion AmpulesCinnabar Dandelion Ampules

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4195-1Cinnabar Dandelion1 mL in 1 AMPULELIQUID11
48951-4195-1Cinnabar Dandelion10 in 1 BOXLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4195CINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]12 package rows20241222_29a2065c-b05a-52f6-e063-6394a90a86cb.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
48951-419548951-4195-1

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
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
LACTOSEJ2B2A4N98GIACT
ELYMUS REPENS ROOT3IXW0F6P8WACTIB
TARAXACUM PALUSTRE ROOTGCZ4W7077CACTIB
FERROUS CATIONGW89581OWRACTIB
CARBONATE ION7UJQ5OPE7DACTIB
MERCURIC CATIONED30FJ8Y42ACTIB

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
29a2033d-82d4-595b-e063-6394a90a44ce29a2065c-b05a-52f6-e063-6394a90a86cb2024-12-19WarningsExact identifier
spl id: 29a2033d-82d4-595b-e063-6394a90a44ce
spl set id: 29a2065c-b05a-52f6-e063-6394a90a86cb

Reported adverse events (FAERS/openFDA)#

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