ULCERPLEX (ANACARDIUM ORIENTALE, ARGENTUM NITRICUM, ARSENICUM ALBUM, ATROPINUM, CARBO VEGETABILIS, GERANIUM MACULATUM, KALI BICHROMICUM, ORNITHOGALUM UMBELLATUM, URANIUM NITRICUM) LIQUID [KIN

ULCERPLEX (ANACARDIUM ORIENTALE, ARGENTUM NITRICUM, ARSENICUM ALBUM, ATROPINUM, CARBO VEGETABILIS, GERANIUM MACULATUM, KALI BICHROMICUM, ORNITHOGALUM UMBELLATUM, URANIUM NITRICUM) LIQUID [KIN
PDF | XML

NDC 57955-0188-2
Set ID f3650b28-68fe-4a61-ba16-4f67d0813203
Category HUMAN OTC DRUG LABEL
Packager King Bio Inc.
Generic Name
Product Class
Product Number
Application Number
  • ACTIVE INGREDIENT

    Drug Facts​__________________________________________________________________________________________________________

    HPUS Active Ingredients: ​Anacardium orientale, Argentum nitricum, Arsenicum album, Atropinum, Carbo vegetabilis, Geranium maculatum, Kali bichromicum, Ornithogalum umbellatum, Uranium nitricum.

    Equal volumes of each ingredient in 10X, 30X, 100X, 1LM, 2LM, 3LM, 5Lm potencies.

  • INDICATIONS & USAGE

    Uses for temporary relief of minor symptoms of: burning, gnawing, or radiating pains in the stomach area, nausea, poor digestion.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Bio-Energetically Enhanced™ pure water, Carya ovata bark extract, citrus extract, Lonicera japonica (honeysuckle), polylysine, steviol glysocsides.

  • WARNINGS

    Warnings

    • Stop use and ask your doctor if symptoms persist or worsen.
    • If pregnant or breast-feeding, take only on advice of a healthcare professional.
  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children.
  • DOSAGE & ADMINISTRATION

    Directions

    • Initially, depress pump until primed.
    • Spray one dose directly into mouth.
    • Adults 12 and up: 3 sprays 3 times per day
    • Children 2-12: 2 sprays 3 times per day
    • Children 2mo.-2yr.: 1 spray 3 times per day
  • OTHER SAFETY INFORMATION

    Tamper resistant for your protection. Use only if safety seal is intact. This product has not been clinically tested.

  • PURPOSE

    Uses ​for temporary relief of minor symptoms of minor symptoms of:

    • burning, gnawing, or radiating pains in the stomach area
    • nausea
    • poor digestion
  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    ULCERPLEX 
    anacardium orientale, argentum nitricum, arsenicum album, atropinum, carbo vegetabilis, geranium maculatum, kali bichromicum, ornithogalum umbellatum, uranium nitricum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57955-0188
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (SEMECARPUS ANACARDIUM JUICE - UNII:Y0F0BU8RDU) SEMECARPUS ANACARDIUM JUICE10 [hp_X]  in 59 mL
    SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE10 [hp_X]  in 59 mL
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE10 [hp_X]  in 59 mL
    ATROPINE (UNII: 7C0697DR9I) (ATROPINE - UNII:7C0697DR9I) ATROPINE10 [hp_X]  in 59 mL
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL10 [hp_X]  in 59 mL
    GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ) (GERANIUM MACULATUM ROOT - UNII:93IXI5B6OJ) GERANIUM MACULATUM ROOT10 [hp_X]  in 59 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE10 [hp_X]  in 59 mL
    ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S) (ORNITHOGALUM UMBELLATUM - UNII:9NS3M2Y78S) ORNITHOGALUM UMBELLATUM10 [hp_X]  in 59 mL
    URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7) URANYL NITRATE HEXAHYDRATE10 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57955-0188-259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/16/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic02/16/2018
    Labeler - King Bio Inc. (617901350)
    Registrant - King Bio Inc. (617901350)
    Establishment
    NameAddressID/FEIBusiness Operations
    King Bio Inc.617901350manufacture(57955-0188)

Related Drugs