Label: NOREPINEPHRINE liquid

  • NDC Code(s): 43742-1319-1
  • Packager: Deseret Biologicals, 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 11, 2022

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  • ACTIVE INGREDIENT:

    Norepinephrine 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

  • HOMEOPATHIC INDICATIONS:

    For temporary relief of symptoms related to Norepinephrine sensitivity including rashes, hives, Premenstrual Syndrome, and headache.**

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

  • WARNINGS:

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

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

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

  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, contact physician or a 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.

  • HOMEOPATHIC INDICATIONS:

    For temporary relief of symptoms related to Norepinephrine sensitivity including rashes, hives, Premenstrual Syndrome, and headache.**

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

  • INACTIVE INGREDIENTS:

    Demineralized Water, 25% Ethanol

  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.
    469 W. Parkland Drive
    Sandy, UT 84070  www.desbio.com

  • PACKAGE LABEL DISPLAY:

    DESBIO
    NDC 43742-1319-1
    HOMEOPATHIC
    NOREPINEPHRINE
    1 FL OZ (30 ml)

    Norepinephrine

  • INGREDIENTS AND APPEARANCE
    NOREPINEPHRINE 
    norepinephrine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-1319
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NOREPINEPHRINE (UNII: X4W3ENH1CV) (NOREPINEPHRINE - UNII:X4W3ENH1CV) NOREPINEPHRINE8 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-1319-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/19/201802/04/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/19/201802/04/2024
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-1319) , api manufacture(43742-1319) , label(43742-1319) , pack(43742-1319)
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