Label: BHI CONSTIPATION- dioscorea villosa tuber, sodium chloride, and strychnos nux-vomica seed 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 July 7, 2022

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

  • ACTIVE INGREDIENTS

    Each tablet contains: *Dioscorea villosa 4X, Natrum muriaticum 200X, *Nux vomica 8X 100 mg each.

    *Natural Ingredients

  • INACTIVE INGREDIENTS

    Inactive Ingredients:Dextrose, Magnesium Stearate, Maltodextrin
    .

  • PURPOSE

    Constipation Relief Tablets

    Relieves:

    • Constipation

    • Bowel Irregularity

    • Bloating

  • USES

    For the temporary relief of minor constipation, bowel irregularity, bloating

  • 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: Take1-2 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 BHI Constipation or any of its ingredients exists.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PRINCIPAL DISPLAY PANEL

    BHI Constipation Tablet

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  • INGREDIENTS AND APPEARANCE
    BHI CONSTIPATION 
    dioscorea villosa tuber, sodium chloride, and strychnos nux-vomica seed tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62795-1005
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8) (DIOSCOREA VILLOSA ROOT - UNII:IWY3IWX2G8) DIOSCOREA VILLOSA TUBER4 [hp_X]
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE200 [hp_X]
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED8 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code Leafman
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62795-1005-31 in 1 CARTON08/30/2014
    1100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/30/2014
    Labeler - MediNatura Inc (079324099)
    Establishment
    NameAddressID/FEIBusiness Operations
    MediNatura102783016manufacture(62795-1005)