Label: BHI SPASM PAIN- atropine sulfate, aconitum napellus, bryonia alba root, citrullus colocynthis fruit pulp, and cupric sulfate tablet

  • 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 September 28, 2023

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  • ACTIVE INGREDIENTS

    Each tablet contains: Atropinum sulphuricum 6X, *Aconitum napellus 4X, *Bryonia alba 4X, *Colocynthis 4X, Cuprum sulphuricum 6X 60 mg each.

    *Natural Ingredients

  • INACTIVE INGREDIENT

    Inactive Ingredients:Dextrose,  Magnesium Stearate, Maltodextrin

  • PURPOSE

    Cramp/Spasm Relief Tablets

    Relieves:

    • Menstrual Cramps

    • Abdominal Bloating

    • Muscle Spasms

  • INDICATIONS & USAGE

  • DIRECTIONS

    At first sign of symptoms: Adults and children 4 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. 

    Standard dosage: Adults and children 4 years and older: Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours.

    For children under 4, consult your health professional.

    Allow tablets to dissolve completely in the mouth, do not swallow.

  • WARNINGS

    If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to Spasm Pain or any of its ingredients exists.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PRINCIPAL DISPLAY PANEL

    BHI Spasm Pain Tablet.jpg

    Add image transcription here...

  • INGREDIENTS AND APPEARANCE
    BHI SPASM PAIN 
    atropine sulfate, aconitum napellus, bryonia alba root, citrullus colocynthis fruit pulp, and cupric sulfate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62795-1015
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ATROPINE SULFATE (UNII: 03J5ZE7KA5) (ATROPINE - UNII:7C0697DR9I) ATROPINE SULFATE6 [hp_X]
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS4 [hp_X]
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT4 [hp_X]
    CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17) CITRULLUS COLOCYNTHIS FRUIT PULP4 [hp_X]
    CUPRIC SULFATE (UNII: LRX7AJ16DT) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC CATION6 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code Leafman
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62795-1015-31 in 1 CARTON01/01/2015
    1100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/01/2015
    Labeler - MediNatura Inc (079324099)
    Establishment
    NameAddressID/FEIBusiness Operations
    MediNatura Inc102783016manufacture(62795-1015)
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