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 29, 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 solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0093-9614 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 0.005 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0093-9614-13 960 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/1991 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 01/01/1991 Labeler - Teva Pharmaceuticals USA, Inc. (001627975)
