Label: BARYTA MURIATICA- barium chloride dihydrate pellet

  • NDC Code(s): 68428-250-03, 68428-250-05, 68428-250-06, 68428-250-11, view more
    68428-250-12
  • Packager: Washington Homeopathic Products
  • 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 May 18, 2018

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

  • ACTIVE INGREDIENTS

    BARYTA MUR

    Close
  • USES

    To relieve the symptoms of large tonsils.

    Close
  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of reach of children.

    Close
  • INDICATIONS

    Indications:

    BARYTA MUR   Buzzing in ears

    Close
  • STOP USE AND ASK DOCTOR

    If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

    Close
  • DIRECTIONS

    Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

    Close
  • INACTIVE INGREDIENTS

    Sucrose/Lactose

    Close
  • PRINCIPAL DISPLAY PANEL

    The OTC potency range of BARYTA MUR is 6x–30x, 3c–30c, 200c, 1m, 10m, 50m, and CM.

    Availability is subject to change.

    Label

    All WHP single remedies are made to order; thus, the labels are printed on the same label stock as the orders are filled.

    ‘Bottle Size’ and ‘Potency’ vary on the label depending on customer choice.

    Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

    Close
  • INGREDIENTS AND APPEARANCE
    BARYTA MURIATICA 
    barium chloride dihydrate pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68428-250
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BARIUM CHLORIDE DIHYDRATE (UNII: EL5GJ3U77E) (BARIUM CATION - UNII:V645272HLN) BARIUM CHLORIDE DIHYDRATE 30 [hp_C]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    Color white (white) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68428-250-03 75 in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/15/2009
    2 NDC:68428-250-05 150 in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/15/2009
    3 NDC:68428-250-11 300 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/15/2009
    4 NDC:68428-250-12 600 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/15/2009
    5 NDC:68428-250-06 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/15/2009
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 12/15/2009
    Labeler - Washington Homeopathic Products (084929389)
    Registrant - Washington Homeopathic Products (084929389)
    Establishment
    Name Address ID/FEI Business Operations
    Washington Homeopathic Products 084929389 manufacture(68428-250)
    Close