STYPTSTIX

Manufacturer
Henry Schein Inc.
Effective date
2025-07-17
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 21:39:34

Label at a glance#

ProductSTYPTSTIX
Active ingredientSILVER NITRATE, POTASSIUM NITRATE
Label structure8 sections

Indications and uses

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...

Storage and handling

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.

Label contents#

Full prescribing information#

INDICATIONS AND USAGE:

INDICATIONS & USAGE SECTION

For cauterization of skin or mucous membrane and for removing warts and granulated tissue.

DOSAGE AND ADMINISTRATION:

DOSAGE & ADMINISTRATION SECTION

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:

DOSAGE FORMS & STRENGTHS SECTION

Stick: 50 mg

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

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:

WARNINGS AND PRECAUTIONS SECTION

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:

STORAGE AND HANDLING SECTION

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:

DISPOSAL AND WASTE HANDLING

Expired or unused applicators may be disposed of according to applicable federal, state and local regulations.

PACKAGE LABEL PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1117536potassium nitrate 25 % / silver nitrate 75 % Medicated PadPSN6
1536601StyptStix 25 % / 75 % Medicated PadPSN6
1536601potassium nitrate 250 MG/ML / silver nitrate 750 MG/ML Medicated Pad [Styptstix]SBD6
1117536potassium nitrate 250 MG/ML / silver nitrate 750 MG/ML Medicated PadSCD6
1117536K+ nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY6
1536601K+ nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated Pad [Styptstix]SY6
1117536Pot nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY6
1536601Pot nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated Pad [Styptstix]SY6
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SpongeSY6
1117536potassium nitrate 25 % / silver nitrate 75 % Topical StickSY6
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SwabSY6
1536601StyptStix (potassium nitrate 250 MG/ML / Silver Nitrate 750 MG/ML) Topical ApplicatorSY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0404-1000-03STYPTSTIX100 in 1 TUBESTICK1006

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
POTASSIUM NITRATEACTIVE INGREDIENTRU45X2JN0Z2
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZE2
NITRATE IONACTIVE MOIETYT93E9Y28442
SILVER CATIONACTIVE MOIETY57N7B0K90A2

Products#

Every source-derived product name is available through these pages.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0404-10000404-1000-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
STYPTSTIXSILVER NITRATE APPLICATORHenry Schein Inc.b7634e27-3c75-4e56-ab42-3e5796edb0c72025-07-17WarningsExact identifier
ndc (package): 0404-1000-03
ndc (product): 0404-1000
ndc11 (package): 00404100003
spl id: e73f2557-ffe1-4333-a31c-c997e9f6ed08
spl set id: b7634e27-3c75-4e56-ab42-3e5796edb0c7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.