Label: DOPAMINE- dopamine hydrochloride liquid

  • NDC Code(s): 43742-0403-1
  • 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 October 25, 2018

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

  • ACTIVE INGREDIENTS:

    Dopamine Hydrochloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

  • INDICATIONS:

    For temporary relief of symptoms including arrhythmia, anxiety, depression, headache, reading difficulty, trembling of limbs, and poor memory.

  • WARNINGS:

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

  • 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

  • KEEP OUT OF REACH OF CHILDREN:

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

  • INDICATIONS:

    For temporary relief of symptoms including arrhythmia, anxiety, depression, headache, reading difficulty, trembling of limbs, and poor memory.

  • QUESTIONS:

    Dist By: Deseret Biologicals, Inc.

    469 Parkland Drive

    Sandy, UT 84070 www.desbio.com

  • Package Label Display:

    DESBIO

    NDC 43742-0403-1

    HOMEOPATHIC

    DOPAMINE

    1 FL OZ (30 ml)

    Dopamine

  • INGREDIENTS AND APPEARANCE
    DOPAMINE 
    dopamine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0403
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOPAMINE HYDROCHLORIDE (UNII: 7L3E358N9L) (DOPAMINE - UNII:VTD58H1Z2X) DOPAMINE HYDROCHLORIDE6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-0403-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product03/14/201408/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/14/201408/05/2020
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca, Inc. (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company, Inc.844330915manufacture(43742-0403) , api manufacture(43742-0403) , label(43742-0403) , pack(43742-0403)