Label: LYCOPODIUM BERBERIS- lycopodium berberis 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 April 27, 2018

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

  • 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: Carduus marianus (Milk thistle) 1X, Berberis (Barberry) 3X, Lycopodium (Club moss) 3X, Chelidonium (Greater celandine) 5X, Curcuma (Turmeric) 5X, Fragaria (Wild strawberry) 5X, Vitis (Grape vine) 5X, Natrium sulf. (Sodium sulfate) 6X, Mercurius dulcis (Mercurous chloride) 10X

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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: 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. 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.

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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
    LYCOPODIUM BERBERIS 
    lycopodium berberis pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-6049
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MILK THISTLE (UNII: U946SH95EE) (MILK THISTLE - UNII:U946SH95EE) MILK THISTLE 1 [hp_X]
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 3 [hp_X]
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 3 [hp_X]
    CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N) (CHELIDONIUM MAJUS ROOT - UNII:FLT36UCF0N) CHELIDONIUM MAJUS ROOT 5 [hp_X]
    TURMERIC (UNII: 856YO1Z64F) (TURMERIC - UNII:856YO1Z64F) TURMERIC 5 [hp_X]
    FRAGARIA VESCA WHOLE (UNII: 5J340B7H82) (FRAGARIA VESCA WHOLE - UNII:5J340B7H82) FRAGARIA VESCA WHOLE 5 [hp_X]
    VITIS VINIFERA LEAF (UNII: R1H893D80E) (VITIS VINIFERA LEAF - UNII:R1H893D80E) VITIS VINIFERA LEAF 5 [hp_X]
    SULFIDE ION (UNII: G15I91XETI) (SULFIDE ION - UNII:G15I91XETI) SULFIDE ION 6 [hp_X]
    CALOMEL (UNII: J2D46N657D) (CALOMEL - UNII:J2D46N657D) CALOMEL 10 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    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:48951-6049-2 1350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/01/2009
    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(48951-6049)
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