Label: KALI BICHROMICUM- potassium dichromate pellet

  • NDC Code(s): 68428-449-03, 68428-449-05, 68428-449-06, 68428-449-11, view more
    68428-449-12
  • Packager: Washington Homeopathic Products
  • Category: HUMAN OTC DRUG LABEL

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 October 19, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENTS

    KALI BIC

  • USES

    To relieve the symptoms of sinuses.

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of reach of children.

  • INDICATIONS

    Indications:

    KALI BIC   Sinuses

  • STOP USE AND ASK DOCTOR

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

  • 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.

  • INACTIVE INGREDIENTS

    Sucrose/Lactose

  • PRINCIPAL DISPLAY PANEL

    The OTC potency range of KALI BIC is 3x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.
    KaliBic2023
    Availability is subject to change.

    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.

  • INGREDIENTS AND APPEARANCE
    KALI BICHROMICUM 
    potassium dichromate pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68428-449
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE30 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Colorwhite (white) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68428-449-0375 in 1 VIAL, GLASS; Type 0: Not a Combination Product02/03/2010
    2NDC:68428-449-05150 in 1 VIAL, GLASS; Type 0: Not a Combination Product02/03/2010
    3NDC:68428-449-11300 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product02/03/2010
    4NDC:68428-449-12600 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product02/03/2010
    5NDC:68428-449-061200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product02/03/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic02/03/2010
    Labeler - Washington Homeopathic Products (084929389)
    Establishment
    NameAddressID/FEIBusiness Operations
    Washington Homeopathic Products084929389manufacture(68428-449)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!