Label: GUN POWDER 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 December 11, 2020

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  • ACTIVE INGREDIENT

    Potassium Nitrate 3X, Charcoal 3X, Sulphur 3X

  • INACTIVE INGREDIENT

    Lactose

  • WARNINGS

    Stop use and ask doctor if symptoms worsen or persist longer than 7 days.

    Do not use if tamper evident seal is missing or broken.

  • INDICATIONS & USAGE

    Temporary relief from skin problems, boils, cuts, deep injuries, animal bites

  • PURPOSE

    Temporary relief of skin problems, boils, cuts, deep injuries, animal bites

  • DOSAGE & ADMINISTRATION

    Adults and children 12 years of age and older: Take 2 talbets three times a day or as prescribed by doctor.

    Children 2 years to 12 years of age: Take 1-2 tablets two to three time pers day or as prescribed by doctor.

    Children under 2 years of age: Consult doctor prior to use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PRINCIPAL DISPLAY PANEL

    gunpowder.jpg

  • INGREDIENTS AND APPEARANCE
    GUN POWDER 
    gun powder tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79718-0061(NDC:79769-0061)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE3 [hp_X]
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL3 [hp_X]
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR3 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code SBL
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79718-0061-1900 in 1 JAR; Type 0: Not a Combination Product12/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/07/2020
    Labeler - Warsan Homeopathic (081031642)
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