Label: GERMPROOF- argentum metallicum gel

  • NDC Code(s): 72363-006-02, 72363-006-03
  • Packager: AG Essence
  • 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 March 10, 2022

If you are a consumer or patient please visit this version.

  • DOSAGE & ADMINISTRATION

    Directions:

    If applying Germproof to a wound or other skin ailment, clean affected area first and rinse with water. Spray enough to lightly cover the afected area and allow to dry. Cover with a sterile dressing if necessary. If condition worsens or does not improve within 7 days consult a doctor.

    Indication for use:

    For relief of these symptoms due to minor wounds, burns, scrapes, ulcerations or minor infections.

    Disclaimer: These statements have not been evaluated by the FDA . This product is not intended to diagnose, treat, cure or prevent any desease.

  • WARNINGS

    Warnings:

    For External Use Only

    Keep out of reach of children

  • INDICATIONS & USAGE

    Indications for use:

    For relief of these symptoms due to minor wounds, burns, scrapes, ulcerations or minor infections.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • PURPOSE

    Purpose

    Gel Wound Dressing

    Homeopathic medicine.

  • ACTIVE INGREDIENT

    ACTIVE: Argentum Metallicum 10x, 20x and 30x HPUS

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Complex Ag21, Water, Polycationic polymers, L-Arginine

  • Germproof Spray Gel Box

    Germproof Spray Gel Box

  • INGREDIENTS AND APPEARANCE
    GERMPROOF 
    argentum metallicum gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72363-006
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.285 g  in 28.5 g
    WATER (UNII: 059QF0KO0R) 27.13 g  in 28.5 g
    ARGININE (UNII: 94ZLA3W45F) 0.085 g  in 28.5 g
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72363-006-031 in 1 BOX03/14/202203/14/2025
    1NDC:72363-006-0228.5 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/14/202203/14/2025
    Labeler - AG Essence (068562165)