Label: CORALLIUM RUBRUM- corallium rubrum 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 15, 2013

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

  • ACTIVE INGREDIENT HPUS

    CORALLIUM RUBRUM 8X

    Red Coral

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  • PURPOSE

    SPASMODIC COUGH*

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  • USE

    For self-limiting condition listed above or as directed by a health professional.

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  • WARNINGS

    Do not use if pellet-dispenser seal is broken.

    Stop use and ask a doctor if symptoms persist more than 3 days or worsen.

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children.

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  • DIRECTIONS

    Adults: Allow 3 or 4 pellets to dissolve in the mouth 3 times a day until symptoms are relieved or as directed by a health professional.

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  • OTHER INFORMATION

    Store at room temperature.

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  • INACTIVE INGREDIENTS

    Lactose, sucrose.

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  • REFERENCES

    The letters 'HPUS' indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

    *These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.

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  • DESCRIPTION

    80 Pellets

    Pellet dispenser

    Mfd for: HOMEOLAB USA

    3025 De L'Assomption, Montreal, QC, H1N 2H2, CANADA

    1-800-404-4666 / www.homeolab.com

    Product of Canada

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  • LABEL
  • INGREDIENTS AND APPEARANCE
    CORALLIUM RUBRUM 
    corallium rubrum pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-6055
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (CORALLIUM RUBRUM EXOSKELETON - UNII:2CA71K0DLE) CORALLIUM RUBRUM EXOSKELETON 8 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    SUCROSE (UNII: C151H8M554)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:60512-6055-1 80 in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 10/11/1995
    Labeler - HOMEOLAB USA INC. (202032533)
    Registrant - HOMEOLAB USA INC. (202032533)
    Establishment
    Name Address ID/FEI Business Operations
    HOMEOLAB USA INC. 202032533 manufacture(60512-6055)
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