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.
  • INDICATIONS AND USAGE

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


  • 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.
  • 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.
  • 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.
  • INACTIVE INGREDIENT

    Inactive ingredients: Ethanol, Purified Water USP.
  • PURPOSE

    Headache rising from the neck, Rheumatic pain in the neck, shoulders and back, Sciatic neuralgia
  • PRINCIPAL DISPLAY PANEL

    Cimicifuga Homaccord Oral Drop.jpg


  • INGREDIENTS AND APPEARANCE
    CIMICIFUGA HOMACCORD 
    black cohosh and strontium carbonate and liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50114-1220
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9) BLACK COHOSH2 [hp_X]  in 50 mL
    STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (CARBONATE ION - UNII:7UJQ5OPE7D) STRONTIUM CARBONATE8 [hp_X]  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50114-1220-450 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/31/1986
    Labeler - Heel Inc (102783016)
    Establishment
    NameAddressID/FEIBusiness Operations
    Heel Inc102783016manufacture
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