Label: SILVER NITRATE solution

  • 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 October 30, 2024

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  • DESCRIPTION

    Silver nitrate solution is a 0.5% solution of silver nitrate in a water medium. It is a topical anti-infective.

  • WARNINGS

    When ingested, silver nitrate is highly toxic to the gastrointestinal tract and central nervous system. Swallowing can cause severe gastroenteritis that may end fatally. Sodium chloride may be used by gastric lavage to remove chemical. Caustic and irritating to the skin and mucous membranes.

  • PRECAUTIONS

    Silver nitrate solution must be handled carefully, since it tends to stain the skin, utensils, clothing and linens.

  • DOSAGE

    Topical as directed by the physician.

    KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

  • SPL UNCLASSIFIED SECTION

    Manufactured By:
    HALO PHARMACEUTICALS
    30 N Jefferson Road
    Whippany, NJ 07981

    Distributed by:
    Genus Lifesciences Inc.
    Allentown, PA 18102

    Rev. 08/24

  • PRINCIPAL DISPLAY PANEL - 960 mL Bottle Label

    NDC 64950-378-96

    Silver Nitrate
    Solution

    0.5%

    FOR EXTERNAL USE ONLY.

    Rx Only
    960 mL (32 fl oz)

    Genus
    Lifesciences Inc.

    PRINCIPAL DISPLAY PANEL - 960 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    SILVER NITRATE 
    silver nitrate solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:64950-378
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Silver Nitrate (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) Silver Nitrate0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64950-378-96960 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other11/01/2024
    Labeler - Genus Lifesciences (113290444)