Label: HISTAMINE- histaminum hydrochloricum liquid

  • NDC Code(s): 43742-0696-1
  • 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 March 14, 2024

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  • ACTIVE INGREDIENTS:

    Histaminum Hydrochloricum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

  • PURPOSE:

    Histaminum Hydrochloricum - Hay Fever, Congestion, Stomach Discomfort

  • USES:

    • For the temporary relief of symptoms including:

    • hay fever • congestion • stomach discomfort

    These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

  • WARNINGS:

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

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

    Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

  • KEEP OUT OF REACH OF CHILDREN:

    In case of overdose, contact a physician or Poison Control Center right away.

  • 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.

  • INACTIVE INGREDIENTS:

    Demineralized water, 25% ethanol

  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.

    469 W. Parkland Drive

    Sandy, UT 84070

    www.desbio.com

    800-827-8204

  • PACKAGE LABEL DISPLAY:

    DesBio

    Histamine

    Homeopathic

    NDC 43742-0696-1

    1 FL OZ (30 ml)

    Histamine

  • INGREDIENTS AND APPEARANCE
    HISTAMINE 
    histaminum hydrochloricum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0696
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-0696-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product12/09/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/09/2015
    Labeler - Deseret Biologials, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-0696) , api manufacture(43742-0696) , label(43742-0696) , pack(43742-0696)
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