Label: SILVER NITRATE solution

  • NDC Code(s): 0093-9614-13
  • Packager: Teva Pharmaceuticals USA, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated February 1, 2016

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  • SPL UNCLASSIFIED SECTION

    Silver Nitrate Solution 0.5% 960 mL Label Text

    NDC 0093-9614-13

    Silver Nitrate

    Solution

    0.5%

    FOR EXTERNAL USE ONLY.

    Rx only

    960 mL (32 fl oz)

    TEVA

    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 the 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.

    Store at 20° to 25°C (68° to 77°F) [See USP Controlled

    Room Temperature]. Do not freeze. Protect from light.

    KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH

    OF CHILDREN.

    Manufactured By:

    HALO PHARMACEUTICALS

    30 N Jefferson Road

    Whippany, NJ 07981

    Manufactured For:

    TEVA PHARMACEUTICALS USA, INC.

    North Wales, PA 19454

    333-32-101019 Rev. E 2/2016
    102121 0786-01

  • Package/Label Display Panel

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  • INGREDIENTS AND APPEARANCE
    SILVER NITRATE 
    silver nitrate solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0093-9614
    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:0093-9614-13960 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/1991
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/1991
    Labeler - Teva Pharmaceuticals USA, Inc. (001627975)