Label: EPINEPHRINE - epinephrine liquid 

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

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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 LABEL Item Code (Source) NDC:57520-0725
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPINEPHRINE (EPINEPHRINE) EPINEPHRINE 200 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    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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