Label: K FLUSH- belladonna, berberls vulgarls, cantharis, , hydrangea, parelra brava, rubla tinct, solidago, sarsaparilla, urtica urens syrup

  • NDC Code(s): 82797-125-12
  • Packager: Dr. Masood Homeopathic Pharmaceuticals Private Limited
  • 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 April 4, 2024

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

  • DOSAGE & ADMINISTRATION

    1 tablespoon full 4 times daily or as directed by homeopathic physician

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Sucrose, Sodium Benzoate, Sorbitol, Citric acid, Cellulose Gum 7HF, Glycerin, Purified Water

  • INDICATIONS & USAGE

    It is indicated for removal of kidney, ureter and bladder stones as well as related infection, inflammation and burning sensation during urination.

  • ACTIVE INGREDIENT

    Belladonna , Berberls Vulgaris, Cantharis , Hydrangea, Parelra Brava, Rubia Tinct, Solidago, Sarsaparilla, Urtica Urens

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PURPOSE

    Active Ingredients Purpose

    Belladonna 8x Cystitis, burning pain in urinary tract. Acute Urinary Infections. Spasmodic pains along ureter

    Berberls Vulgarls Used for Renal troubles

    Cantharis Helps control frequency and urgency of urine

    Hydrangea Renal colic

    Parelra Brava Useful in renal colic, prostatic affection and catarrh of the bladder

    Rubia Tinct Cures bladder stones

    Solidago Renal coilic with dysuria

    Sarsaparilla Renal colic

    Urtica Urens Helps control urinary tact infection

  • WARNINGS

    Warnings:

    Do not:

    • use if you have an allergy or hypersensitivity to components of the formula
    • use if pregnant or nursing

    Stop use and ask a doctor if:

    • condition worsens
    • If symptoms persists for more than 7 days

  • PRINCIPAL DISPLAY PANEL

    K Flush Syrup

  • INGREDIENTS AND APPEARANCE
    K FLUSH 
    belladonna, berberls vulgarls, cantharis, , hydrangea, parelra brava, rubla tinct, solidago, sarsaparilla, urtica urens syrup
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82797-125
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BELLADONNA LEAF (UNII: 6GZW20TIOI) (BELLADONNA LEAF - UNII:6GZW20TIOI) BELLADONNA LEAF0.12 mg  in 120 mL
    HYDRANGEA ARBORESCENS BARK (UNII: MRX3W33KCB) (HYDRANGEA ARBORESCENS BARK - UNII:MRX3W33KCB) HYDRANGEA ARBORESCENS BARK0.492 mg  in 120 mL
    URTICA URENS FLOWER (UNII: 3641X02D5V) (URTICA URENS FLOWER - UNII:3641X02D5V) URTICA URENS FLOWER0.24 mg  in 120 mL
    SARSAPARILLA (UNII: 2H1576D5WG) (SARSAPARILLA - UNII:2H1576D5WG) SARSAPARILLA0.24 mg  in 120 mL
    SOLIDAGO CANADENSIS FLOWERING TOP (UNII: ZHL562L3PR) (SOLIDAGO CANADENSIS FLOWERING TOP - UNII:ZHL562L3PR) SOLIDAGO CANADENSIS FLOWERING TOP0.24 mg  in 120 mL
    BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3) (BERBERIS VULGARIS FRUIT - UNII:6XEF22AHC3) BERBERIS VULGARIS FRUIT1.7 mg  in 120 mL
    LYTTA VESICATORIA (UNII: 3Q034RO3BT) (LYTTA VESICATORIA - UNII:3Q034RO3BT) LYTTA VESICATORIA0.492 mg  in 120 mL
    RUBIA CORDIFOLIA ROOT (UNII: 4V873H15CG) (RUBIA CORDIFOLIA ROOT - UNII:4V873H15CG) RUBIA CORDIFOLIA ROOT0.24 mg  in 120 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.06 mg  in 120 mL
    SUCROSE (UNII: C151H8M554) 42 mg  in 120 mL
    SODIUM BENZOATE (UNII: OJ245FE5EU) 0.42 mg  in 120 mL
    SORBITOL SOLUTION 70% (UNII: 8KW3E207O2) 18 mL  in 120 mL
    GLYCERIN (UNII: PDC6A3C0OX) 12 mL  in 120 mL
    WATER (UNII: 059QF0KO0R) 120 mL  in 120 mL
    .ALPHA.-CELLULOSE (UNII: I355QGZ19A) 0.48 mg  in 120 mL
    Product Characteristics
    ColorpinkScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82797-125-12120 mL in 1 BOTTLE; Type 0: Not a Combination Product04/04/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/04/2024
    Labeler - Dr. Masood Homeopathic Pharmaceuticals Private Limited (645453119)
    Registrant - Dr, Masood Homeopathic Pharmaceuticals Private Limited (645453119)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dr. Masood Homeopathic Pharmaceuticals Private Limited645453119manufacture(82797-125) , pack(82797-125) , label(82797-125)