Label: SOVEREIGN SILVER - silver gel

  • NDC Code(s): 52166-002-01, 52166-002-02
  • Packager: Natural Immunogenics Corp.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

Drug Label Information

Updated 04/13

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  • ACTIVE INGREDIENT

    Ingredients: ACTIVE:

    Argentum Metallicum 10x, 20x and 30x HPUS

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  • INACTIVE INGREDIENT

    INACTIVE: Silver hydrosol,

    carbopol and sodium hydroxide


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  • PURPOSE

    Purpose

    First Aid Gel

    Homeopathic medicine

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    Adult supervision required

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  • WARNINGS

    Warnings. For external

    use only. Ask a doctor before use if

    you have deep or puncture wounds, animal bites or serious burns.

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  • ASK DOCTOR

    Stop and ask a doctor if

    symptoms persist or worsen after 3 days of use. Do not use if

    seal is broken

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  • DOSAGE & ADMINISTRATION

    Enter section text here Directions. Clean affected area.

    Apply a liberal, consistent layer of First Aid Gel. Leave wet or bandage for

    optimal results. Repeat 3 times per day or as often as needed to relieve symptoms.

    For sensitive skin.

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  • INDICATIONS & USAGE

    Indications for Use: For relief of these symptoms due to

    minor wounds and burns, bruises, ulcerations, sunburn, razor burns,

    scrapes, rashes, blisters, bug bites and skin eruptions from acne, eczema

    or minor infection:

    burning

    stinging

    itching

    redness

    stiffness

    minor pain

    minor inflammation

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  • INGREDIENTS AND APPEARANCE
    SOVEREIGN SILVER  
    argentum metallicum gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:52166-002
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Silver (UNII: 3M4G523W1G) (Silver - UNII:3M4G523W1G) Silver 30 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  
    Sodium hydroxide (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52166-002-02 1 in 1 BOX
    1 NDC:52166-002-01 1 in 1 BOX
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/01/2009
    Labeler - Natural Immunogenics Corp. (048744085)
    Registrant - Natural Immunogenics Corp. (048744085)
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