Home > Drugs A-Z > KALI SULPH

KALI SULPH (Hyland's)

Available Formats

Dosage Form Package Information Links
TABLET 1000 TABLET in 1 BOTTLE, PLASTIC (54973-3107-2) Label Information
TABLET 500 TABLET in 1 BOTTLE, PLASTIC (54973-3107-1) Label Information

Complete KALI SULPH Information

  • DIRECTIONS

    Adults & Children ages 6 - 12: 4 tablets. Children ages 2 - 6: 2 tablets. Dissolve under tongue 3 times a day. Use more frequently (every 15 minutes for up to 8 doses) with acute conditions.


  • INDICATIONS

    Relief of symptoms of the common cold. Relief of symptoms of pimples and blemishes associated with common acne.


  • FORMULA

    Kali Sulphuricum 30X HPUS

    in a base of Acacia Gum, Lactose N.F.


  • Warnings

    Do not use if imprinted cap band is broken or missing.

    If symptoms persist for more than seven days or worsen, contact a licensed health care provider.

    Discontinue use if symptoms are accompanied by a high fever (over 101° F).

    If you are pregnant or nursing, seek the advice of a licensed health care provider before using this product.

    Keep this and all medications out of the reach of children.


  • QUESTIONS?

    800.624.9659


  • PRINCIPAL DISPLAY PANEL - 500 Tablet Bottle Label

    HOMEOPATHIC

    NDC 54973-3107-01

    Hyland's®

    #7

    Kali Sulph. 30X

    Colds,
    Skin Eruptions

    500 TABLETS

    label


  • INGREDIENTS AND APPEARANCE
    KALI SULPH 
    potassium sulfate tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-3107
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 30 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    ACACIA (UNII: 5C5403N26O)  
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    Color white Score no score
    Shape ROUND Size 9mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:54973-3107-1 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1940
    2 NDC:54973-3107-2 1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1940 12/31/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/01/1940
    Labeler - Hyland's (028570695)
    Establishment
    Name Address ID/FEI Business Operations
    Standard Homeopathic Company 008316655 manufacture(54973-3107) , pack(54973-3107)