OCTOPAMINE (OCTOPAMINE (HYDROCHLORIDE)) LIQUID [DESERET BIOLOGICALS, INC.]

OCTOPAMINE (OCTOPAMINE (HYDROCHLORIDE)) LIQUID [DESERET BIOLOGICALS, INC.]
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NDC 43742-0975-1
Set ID 6fb6fdff-fefa-4d33-ba3a-68ac4a840412
Category HUMAN OTC DRUG LABEL
Packager Deseret Biologicals, Inc.
Generic Name
Product Class
Product Number
Application Number
  • ACTIVE INGREDIENT:

    Octopamine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

  • HOMEOPATHIC INDICATIONS:

    For the temporary relief of headaches, indigestion, and mental sluggishness.**

    **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 the temporary relief of headaches, indigestion, and mental sluggishness.**

    **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 43742-0975-1

    HOMEOPATHIC

    OCTOPAMINE

    1 FL OZ (30 ml)

    Octopamine

  • INGREDIENTS AND APPEARANCE
    OCTOPAMINE 
    octopamine (hydrochloride) liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0975
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOPAMINE HYDROCHLORIDE (UNII: 37YAS5L9HQ) (OCTOPAMINE - UNII:14O50WS8JD) OCTOPAMINE 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:43742-0975-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product02/16/201703/16/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic02/16/201703/16/2022
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-0975) , api manufacture(43742-0975) , label(43742-0975) , pack(43742-0975)

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