Silver Nitrate by Teva Pharmaceuticals USA, Inc. SILVER NITRATE solution

Silver Nitrate by

Drug Labeling and Warnings

Silver Nitrate by is a Prescription medication manufactured, distributed, or labeled by Teva Pharmaceuticals USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

SILVER NITRATE 
silver nitrate solution

Product 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)