Label: BANDA-SIL LIQUID GEL- argentum metallicum gel

  • 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 April 19, 2024

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  • DOSAGE & ADMINISTRATION

    Directions For Use:

    Clear wound area of dirt and debris.

    Spray the affected area with Banda-Sil Silver Liquid Gel Spray and allow to dry.

    Cover with a sterile gauze or appropriate secondary dressing and secure in place.

    Reapply 1-3 times daily or as needed.

    Between dressing changes maintain a moist wound environment.

  • WARNINGS

    Warnings:

    For External Use Only. Keep out of reach of children.

    Consult a doctor if condition worsens or does not improve in seven (7) days. Ask a doctor before use if you have deep or puncture wounds, serious bleeding, or servious burns.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Complex AG21, Water, Polycationic Polymers, Glycerin, L-Arginine

  • INDICATIONS & USAGE

    Indications for use:

    For relief of these symptoms due to minor wounds, burns, scrapes ulcerations,or minor infections, burning, stinging, itching, redness, minor pain, minor inflammation.

  • KEEP OUT OF REACH OF CHILDREN

    Warnings:

    For External Use Only. Keep out of reach of children.

  • PURPOSE

    Topical Antiseptic

  • ACTIVE INGREDIENT

    Active Ingredient

    Argentum Metallicum (Metallic Silver 10X 20X 30X HPUS)

  • Banda-Sil Spray Gel Box

    Banda-Sil Spray Gel Box

  • INGREDIENTS AND APPEARANCE
    BANDA-SIL LIQUID GEL 
    argentum metallicum gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72363-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER1 g  in 28.5 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 27.13 g  in 28.5 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.285 g  in 28.5 g
    ARGININE (UNII: 94ZLA3W45F) 0.085 g  in 28.5 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72363-005-031 in 1 BOX06/25/2021
    128.5 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/25/2021
    Labeler - AG Essence Inc (068562165)
    Establishment
    NameAddressID/FEIBusiness Operations
    AG Essence Inc068562165manufacture(72363-005)
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