Label: CHELIDONIUM CURCUMA P- chelidonium curcuma p liquid

  • 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 24, 2018

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

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  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

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  • ACTIVE INGREDIENT

    Active Ingredients: 100gm contains: 25gm Chelidonium (Greater celandine) 1X, 25gm Curcuma (Turmeric) 1X

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  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Propolis

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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. 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.

    REFRIGERATE AFTER OPENING.
    BEST WHEN USED WITHIN 30 DAYS OF OPENING.

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  • QUESTIONS

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

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  • INGREDIENTS AND APPEARANCE
    CHELIDONIUM CURCUMA P 
    chelidonium curcuma p liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-3154
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N) (CHELIDONIUM MAJUS ROOT - UNII:FLT36UCF0N) CHELIDONIUM MAJUS ROOT 1 [hp_X]  in 1 mL
    TURMERIC (UNII: 856YO1Z64F) (TURMERIC - UNII:856YO1Z64F) TURMERIC 1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-3154-3 60 mL in 1 BOTTLE, DROPPER; 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(48951-3154)
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