Label: EPINEPHRINE - epinephrine liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

Drug Label Information

Updated 07/11

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  Adrenalinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.


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  • PURPOSE

    INDICATIONS:  For the temporary relief of symptoms including anxiety attacks, exhaustion, hypotension, chest pain and congestion, asthma and stress.


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  • WARNINGS

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


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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 the temporary relief of symptoms including anxiety attacks, exhaustion, hypotension, chest pain and congestion, asthma and stress.


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  • QUESTIONS

    Dist. By:

    Deseret Biologicals, Inc.

    469 Parkland Drive

    Sandy, UT 84070

    www.desbio.com


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  • PRINCIPAL DISPLAY PANEL

    DESBIO

    NDC 57520-0725-1

    HOMEOPATHIC

    EPINEPHRINE

    1 FL OZ (30 ml)

    Epinephrine

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  • INGREDIENTS AND APPEARANCE
    EPINEPHRINE 
    adrenalinum, liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0725
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE 200 [hp_C]  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:57520-0725-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 07/07/2011
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture
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