GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE)

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst
Effective date
2024-03-25
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 21:01:17

Label at a glance#

ProductGRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE)
Active ingredientPOTASSIUM NITRATE, SILVER NITRATE
Label structure8 sections

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 & USAGE

INDICATIONS & USAGE SECTION

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

DOSAGE & 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.

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 & 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 returned for disposal to: GF Health Products, Inc., 33 Plan Way, Bldg. # 2, Warwick, RI 02886, or disposed of according to applicable federal, state and local regulations.

HOW SUPPLIED

HOW SUPPLIED SECTION

NDC 51662-1611-1

GRAFCO SILVER NITRATE 6" APPLICATORS (75% SILVER NITRATE, 25% POTASSIUM NITRATE) 100 PER TUBE

HF Acquisition Co LLC, DBA HealthFirst
11629 49th Pl W.

Mukilteo, WA 98275

PRINCIPAL DISPLAY PANEL - NDC 51662-1611-1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

51662-1611-1 Serialized Tube Labeling

Serialized LabelSerialized Label

RFID LabelRFID Label

Tube Labeling

Tube LabelTube Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1117536potassium nitrate 25 % / silver nitrate 75 % Medicated PadPSN2
1117536potassium nitrate 250 MG/ML / silver nitrate 750 MG/ML Medicated PadSCD2
1117536K+ nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY2
1117536Pot nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY2
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SpongeSY2
1117536potassium nitrate 25 % / silver nitrate 75 % Topical StickSY2
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SwabSY2

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
51662-1611-1GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE)100 in 1 TUBESTICK1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51662-1611GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE) STICK [HF ACQUISITION CO LLC, DBA HEALTHFIRST]2Current NDC, Legacy NDC, 1 package rows20240327_e5ebf7aa-fbe5-45b1-e053-2a95a90a5cbf.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
12165-100-01EA - Each12165-1004dfd0c3e-fde0-4008-9609-4b6d6d5aeb3212019-04-11
12165-100-03EA - Each12165-100d56d8ef5-c62c-4095-8b03-90bb229b78f112012-07-24

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51662-161151662-1611-1
12165-100

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE)GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE)HF Acquisition Co LLC, DBA HealthFirste5ebf7aa-fbe5-45b1-e053-2a95a90a5cbf2024-03-25WarningsExact identifier
ndc (package): 51662-1611-1
ndc (product): 51662-1611
ndc11 (package): 51662161101
spl id: 148075f9-33cc-12b0-e063-6294a90a3504
spl set id: e5ebf7aa-fbe5-45b1-e053-2a95a90a5cbf
GRAFCO APPLICATOR 15 CMSILVER NITRATEGF Health Products, Inc.41a82a8c-9a4a-4610-a115-8d8c72a25b1e2021-01-19WarningsExact identifier
ndc (product): 12165-100

Reported adverse events (FAERS/openFDA)#

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