Label: ARGENTYN 23 - argentum metallicaum gel

  • NDC Code(s): 52166-001-01, 52166-001-02
  • Packager: Natural Immunogenics Corp.
  • 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 November 10, 2015

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  • ACTIVE INGREDIENT

    Ingredients: ACTIVE:

    Argentum Mettalicum 10x, 20x and 30x HPUS

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  • INACTIVE INGREDIENT

    Inactive: Silver Hydrosol, carbopol

    and Sodium hydroxide

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  • PURPOSE

     First Aid Gel

    Homeopathic Medicine

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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  • WARNINGS

    Warnings. For external use only.

    Ask a doctor before use of you have deep or puncture wounds,

    animal bites or serious burns.

    Adult supervision required.

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  • DOSAGE & ADMINISTRATION

    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

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  • INDICATIONS & USAGE

    Indications for Use: For relief of these symptoms

    due to minor wounds and burns, bruises, ulcerations,

    sunburn, razor burn, scrapes, rashes, blisters, bug bites,

    and skin eruptions form acne, eczema, or minor infection:

    burning

    stinging

    itching

    redness

    stiffness

    minor pain

    minor inflammation

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  • INGREDIENTS AND APPEARANCE
    ARGENTYN 23  
    argentum metallicaum gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:52166-001
    Route of Administration TOPICAL
    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:52166-001-02 1 in 1 BOX
    1 NDC:52166-001-01 1 in 1 BOX; Type 0: Not a Combination Product
    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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