Label: HISTAMINE- histaminum hydrochloricum liquid

  • NDC Code(s): 43742-0086-1
  • Packager: Deseret Biologials, Inc.
  • 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 November 6, 2018

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

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS: ​Histaminum Hydrochloricum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

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  • PURPOSE

    ​INDICATIONS: ​For temporary relief of hay fever, asthma, congestion, depression, fatigue, hives, hyperactivity, sinusitis and stomach discomfort.

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  • WARNINGS

    WARNINGS: Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

    If pregnant or breast-feeding, seek advice of a health professional before use.

    Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

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  • DOSAGE & ADMINISTRATION

    DIRECTIONS: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:​Demineralized Water, 25% Ethanol

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. In case of overdose, contact physician or Poison Control Center right away.

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  • INDICATIONS & USAGE

    INDICATIONS: For temporary relief of hay fever, asthma, congestion, depression, fatigue, hives, hyperactivity, sinusitis and stomach discomfort.

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  • QUESTIONS

    Dist. By: Deseret Biologicals, Inc.

    469 Parkland Drive

    Sandy, UT 84070

    www.desbio.com

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  • PACKAGE LABEL DISPLAY:

    DESBIO

    NDC 43742-0086-1

    HOMEOPATHIC

    HISTAMINE

    1 FL OZ (30 ml)

    Histamine

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  • INGREDIENTS AND APPEARANCE
    HISTAMINE 
    histaminum hydrochloricum liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0086
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43742-0086-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/16/2012 06/23/2020
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 08/16/2012 06/23/2020
    Labeler - Deseret Biologials, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(43742-0086)
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