STYPTSTIX- silver nitrate applicator stick

STYPTSTIX by

Drug Labeling and Warnings

STYPTSTIX by is a Prescription medication manufactured, distributed, or labeled by Henry Schein Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS AND 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

INGREDIENTS AND APPEARANCE

STYPTSTIX 
silver nitrate applicator stick

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 0404-1000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A)	SILVER NITRATE	38.21 mg
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	12.74 mg

Inactive Ingredients
Ingredient Name	Strength
HYDROCHLORIC ACID (UNII: QTT17582CB)	0.042 mg
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.021 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0404-1000-01	16 in 1 CASE	06/01/2014
1	NDC: 0404-1000-02	12 in 1 BOX
1	NDC: 0404-1000-03	100 in 1 TUBE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/01/2014

Labeler - Henry Schein Inc. (012430880)