Label: AQUILINUM TARAXICUM- chelidonium majus, dryopteris filix-mas root, pteridium aquilinum whole, salix purpurea bark, willow bark, salix alba flower, asplenium scolopendrium top, solidago canadensis flowering top and taraxacum palustre root pellet 

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

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 03/14

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

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  • 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.

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  • ACTIVE INGREDIENT

    Active Ingredients: Chelidonium e flor. 3X, Filix mas e rad. 3X, Pteridium aquil. e fol. 3X, Salix purpurea e fol. 3X, Salix viminalis e fol. 3X, Salix vitellina e fol. 3X, Scolopendrium e fol. 3X, Solidago ex herba 3X, Taraxacum e pl. tota 3X

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  • INACTIVE INGREDIENT

    Inactive Ingredient: Sucrose

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  • PURPOSE

    Use: Temporary relief of digestive upset.

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

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  • WARNINGS

    Warnings: Contains sugar. Diabetics
    and persons intolerant of sucrose (sugar): Consult a doctor before use. 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. Natural ingredients may cause color, scent and/or taste variation.

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  • QUESTIONS

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

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  • INGREDIENTS AND APPEARANCE
    AQUILINUM TARAXICUM 
    aquilinum taraxicum pellet
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:48951-1070
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHELIDONIUM MAJUS (CHELIDONIUM MAJUS) CHELIDONIUM MAJUS 3 [hp_X]
    DRYOPTERIS FILIX-MAS ROOT (DRYOPTERIS FILIX-MAS ROOT) DRYOPTERIS FILIX-MAS ROOT 3 [hp_X]
    PTERIDIUM AQUILINUM WHOLE (PTERIDIUM AQUILINUM WHOLE) PTERIDIUM AQUILINUM WHOLE 3 [hp_X]
    SALIX PURPUREA BARK (SALIX PURPUREA BARK) SALIX PURPUREA BARK 3 [hp_X]
    WILLOW BARK (WILLOW BARK) WILLOW BARK 3 [hp_X]
    SALIX ALBA FLOWER (SALIX ALBA FLOWER) SALIX ALBA FLOWER 3 [hp_X]
    ASPLENIUM SCOLOPENDRIUM TOP (ASPLENIUM SCOLOPENDRIUM TOP) ASPLENIUM SCOLOPENDRIUM TOP 3 [hp_X]
    SOLIDAGO CANADENSIS FLOWERING TOP (SOLIDAGO CANADENSIS FLOWERING TOP) SOLIDAGO CANADENSIS FLOWERING TOP 3 [hp_X]
    TARAXACUM PALUSTRE ROOT (TARAXACUM PALUSTRE ROOT) TARAXACUM PALUSTRE ROOT 3 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE  
    Product Characteristics
    Color white Score no score
    Shape ROUND Size 3mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-1070-2 1350 in 1 BOTTLE, GLASS
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    Name Address ID/FEI Business Operations
    Uriel Pharmacy Inc. 043471163 manufacture(48951-1070)
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