Label: KALI SULF. BATH ESSENCE liquid

  • 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 August 6, 2014

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  • INDICATIONS & USAGE

    Directions: FOR TOPICAL USE ONLY. SHAKE WELL BEFORE USE.

  • DOSAGE & ADMINISTRATION

    For compresses: Use 2 teaspoons per cup of lukewarm water. For full bath: Use 2-3 tablespoons.

  • ACTIVE INGREDIENT

    Active Ingredient: Kalium sulfuratum 1X

  • INACTIVE INGREDIENT

    Inactive Ingredient: Distilled water

  • PURPOSE

    Use: Temporary relief of headache.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: FOR EXTERNAL USE ONLY. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    product label

  • INGREDIENTS AND APPEARANCE
    KALI SULF. BATH ESSENCE 
    kali sulf. bath essence liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-6005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM SULFIDE (UNII: 31R0R7HD0N) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFIDE1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-6005-6125 mL in 1 BOTTLE, GLASS
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-6005)
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