KALI MUR (KALI MURIATICUM) LIQUID [ENERGIQUE, INC.]

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KALI MUR (KALI MURIATICUM) LIQUID [ENERGIQUE, INC.]
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NDC 44911-0166-1
Set ID db9894e6-2de0-428e-b553-11bb39a1d711
Category HUMAN OTC DRUG LABEL
Packager Energique, Inc.
Generic Name
Product Class
Product Number
Application Number
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  • ACTIVE INGREDIENT:

    (in each drop): 100% of Kali Muriaticum 200C.

  • INDICATIONS:

    May temporarily relieve nasal congestion and chronic ear complaints.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • WARNINGS:

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

    Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS:

    Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 4 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

  • INDICATIONS:

    May temporarily relieve nasal congestion and chronic ear complaints.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • INACTIVE INGREDIENTS:

    Demineralized water, 20% Ethanol.

  • QUESTIONS:

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579   800-869-8078

  • PACKAGE LABEL DISPLAY:

    ENERGIQUE

    SINCE 1987

    HOMEOPATHIC REMEDY

    KALI MUR 

    200C

    1 fl. oz. (30 ml)

    Kali Mur 200C

  • INGREDIENTS AND APPEARANCE
    KALI MUR 
    kali muriaticum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0166
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION200 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0166-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/20/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/20/2015
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0166) , api manufacture(44911-0166) , label(44911-0166) , pack(44911-0166)
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