FDA.reportPublic FDA data

Cinnabar Dandelion

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:29:19

Label at a glance#

ProductCinnabar Dandelion
Active ingredientCARBONATE ION, MERCURIC CATION, ELYMUS REPENS ROOT, FERROUS CATION, TARAXACUM OFFICINALE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult
a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Taraxacum (Dandelion) 2X, Agropyrum (Couch grass) 3X, Pyrite (Nat. Iron disulfide) 3X, Kali carb. e cin. Fagi (Potassium carbonate from beech wood ash) 10X, Cinnabaris (Nat. mercuric sulfide) 20X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic sucrose, Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporarily relieves symptoms of cold, flu and sore throat.

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Contains traces of lactose. 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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cinnabar Dandelion PelletsCinnabar Dandelion Pellets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3225-2Cinnabar Dandelion1350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3225CINNABAR DANDELION PELLET [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20241207_7a2b5118-1b6e-1c18-e053-2991aa0a0245.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
48951-322548951-3225-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBONATE ION7UJQ5OPE7DACTIM
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
MERCURIC CATIONED30FJ8Y42ACTIM
SUCROSEC151H8M554IACT
ELYMUS REPENS ROOT3IXW0F6P8WACTIB
FERROUS CATIONGW89581OWRACTIM
TARAXACUM OFFICINALE39981FM375ACTIB

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
2876463f-f78c-dfd9-e063-6394a90aba347a2b5118-1b6e-1c18-e053-2991aa0a02452024-12-04WarningsExact identifier
spl id: 2876463f-f78c-dfd9-e063-6394a90aba34
spl set id: 7a2b5118-1b6e-1c18-e053-2991aa0a0245

Reported adverse events (FAERS/openFDA)#

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