Label: ARGENTYN 23  - silver 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

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 04/13

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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 LABEL Item Code (Source) NDC:52166-001
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Silver (Silver) Silver 30 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)  
    Sodium hydroxide  
    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
    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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