Label: VET ONE- silver nitrate applicator stick

  • Category: HUMAN PRESCRIPTION DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 3, 2019

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  • INDICATIONS & USAGE

    For cauterization of skin or mucous membrane and for removing warts and granulated tissue. 

  • DOSAGE AND ADMINISTRATION:

    Moisten the applicator tip with distilled, deionized or purified water and apply the silver nitrate to the affected area by
    holding, rubbing, or rotating the tip along the affected tissue. The strength of the action is controlled by the dilution with distilled,
    deionized or purified water. One silver nitrate applicator is generally sufficient for each application. The action of the silver nitrate
    can be stopped by washing the area with saline solution (0.9% sodium chloride). Using saline solution to wet the applicator tips,
    or residual saline from wound flushing/washing will interfere with the action of silver nitrate resulting in cauterization failure. Only
    use distilled, deionized or purified water to wet applicator tips. Blot dry wounds that have been flushed/washed with saline prior
    to applying silver nitrate.

  • DOSAGE FORMS AND STRENGTHS:

     Stick: 50 mg

  • CONTRAINDICATIONS:

    Silver salts stain tissue black due to deposition of reduced silver. The stain gradually disappears within a period of two weeks.
    Prolonged ingestion or absorption of silver compounds leads to deposition of silver in connective tissues, producing a slate-blue
    discoloration of the skin known as argyria. This discoloration may also appear on mucous membranes such as the margins of
    gums. The sclera of the eye is also stained.

  • WARNINGS AND PRECAUTIONS:

    WARNING: KEEP OUT OF REACH OF CHILDREN. The active ingredients are poisonous and may be fatal when
    ingested in sufficient doses. The symptoms include toxic gastroenteritis, which may lead to coma, convulsion,
    paralysis and profound alteration of respiration. If poisoning occurs, immediately consult a physician.
    WARNING: DO NOT USE ON THE EYES. In case of eye contact, hold eyes open and immediately flush thoroughly
    with water for at least 15 minutes and consult a physician.
    CAUTION: SILVER NITRATE IS A CAUSTIC SUBSTANCE. Chemical burns may result from inappropriate use of
    product.
    • Wear chemical resistant gloves while using this product. Wear other appropriate personal protective equipment as
    needed.
    • Take care to confine the silver nitrate to the area being treated by using an appropriate physical or chemical barrier to
    prevent staining or burning of untreated tissue.
    • Skin contact time with applicators should be minimal when used on thin delicate skin or neonates.
    • Avoid prolonged contact with skin or other surfaces since staining may occur.
    CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT PRESCRIPTION.

  • STORAGE:

    Store in the closed package at room temperature in a dry place protected from light. Silver nitrate will oxidize and
    turn dark brown upon exposure to light, however this does not affect the product’s potency or utility. Exposure to
    moisture can cause the tip to break or loosen from the applicator. Store away from vaporous chemicals.

  • DISPOSAL:

    Expired or unused applicators may be disposed of according to applicable federal, state and local regulations.

  • PACKAGE LABEL PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    VET ONE 
    silver nitrate applicator stick
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:13985-706
    Route of AdministrationTopical
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE38.21 mg
    POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE12.74 mg
    Inactive Ingredients
    Ingredient NameStrength
    HYDROCHLORIC ACID (UNII: QTT17582CB) 0.036 mg
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.021 mg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13985-706-10100 in 1 TUBE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug01/01/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2010
    Labeler - MWI Veterinary Supply (019926120)
    Registrant - GF Health Products, Inc. (132016168)
    Establishment
    NameAddressID/FEIBusiness Operations
    GF Health Products, Inc.798817599manufacture(13985-706)