Label: CIMICIFUGA HOMACCORD - black cohosh and strontium carbonate and 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 February 28, 2012

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  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of the reach of children. Close
  • INDICATIONS AND USAGE

    For the temporary relief of:
    • Headache rising from the neck
    • Rheumatic pain in the neck, shoulders and back
    • Sciatic neuralgia


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  • WARNINGS

    If symptoms persist or worsen, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product. Close
  • DOSAGE AND ADMINISTRATION

    Adults and children above 11 years: 10 drops orally, 3 times daily, or as directed by a physician. Consult a physician for use in children under 12 years of age. Close
  • ACTIVE INGREDIENT

    Each 50 ml contains as active ingredients: Cimicifuga racemosa 2X, 10X, 30X, 200X 0.4 ml each; Strontium carbonicum 8X, 30X, 200X 0.1 ml each.
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  • INACTIVE INGREDIENT

    Inactive ingredients: Ethanol, Purified Water USP.
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  • PURPOSE

    Headache rising from the neck, Rheumatic pain in the neck, shoulders and back, Sciatic neuralgia
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  • INGREDIENTS AND APPEARANCE
    CIMICIFUGA HOMACCORD 
    black cohosh and strontium carbonate and liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50114-1220
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9) BLACK COHOSH 2 [hp_X]  in 50 mL
    STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (CARBONATE ION - UNII:7UJQ5OPE7D) STRONTIUM CARBONATE 8 [hp_X]  in 50 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50114-1220-4 50 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/31/1986
    Labeler - Heel Inc (102783016)
    Establishment
    Name Address ID/FEI Business Operations
    Heel Inc 102783016 manufacture
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