Label: CINNABAR DANDELION pellet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated November 8, 2018

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    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.

  • ACTIVE INGREDIENT

    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

    Inactive Ingredients: Organic sucrose, Lactose

  • PURPOSE

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

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    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 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.

  • QUESTIONS

    Questions? Call 866.642.2858
    Made by Uriel, East Troy, WI 53120
    www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    Cinnabar Dandelion Pellet

  • INGREDIENTS AND APPEARANCE
    CINNABAR DANDELION 
    cinnabar dandelion pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-3225
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE2 [hp_X]
    CARBONATE ION (UNII: 7UJQ5OPE7D) (CARBONATE ION - UNII:7UJQ5OPE7D) CARBONATE ION10 [hp_X]
    ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) (ELYMUS REPENS ROOT - UNII:3IXW0F6P8W) ELYMUS REPENS ROOT3 [hp_X]
    FERROUS CATION (UNII: GW89581OWR) (FERROUS CATION - UNII:GW89581OWR) FERROUS CATION3 [hp_X]
    MERCURIC CATION (UNII: ED30FJ8Y42) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CATION20 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-3225-21350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-3225)