Silver Nitrate Applicators

Manufacturer
Arzol Chemical Company
Effective date
2025-10-29
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
13
Source
full-release
Hydrated at
2026-05-31 22:03:14

Label at a glance#

ProductSilver Nitrate Applicators
Active ingredientPOTASSIUM NITRATE, SILVER NITRATE
Label structure4 sections

Label contents#

Full prescribing information#

INSTRUCTIONS FOR USE SECTION

Arzol Insert FrontArzol Insert FrontArzol Insert BackArzol Insert Back

STATEMENT OF IDENTITY SECTION

ARZOL® Silver Nitrate Applicators

DOSAGE FORMS & STRENGTHS SECTION

Silver Nitrate 75%

Potassium Nitrate 25%

DESCRIPTION SECTION

for Simplified Silver Nitrate Therapy

ARZOL Silver Nitrate Applicators provide a simple and convenient means of treating small lesions of the skin and mucous membranes. On contact with living tissue, silver nitrate acts as an escharotic. Deep action is avoided by the formation of a dense surface film of coagulated albumin.

Silver nitrate is a powerful chemical germicide. Despite precipitation, it retains substantial germicidal potency even in the presence of large quantities of albuminous material, possibly by gradually redissolving the silver.

SPECIAL PROPERTIES

GENERAL PRECAUTIONS SECTION

The combination of silver nitrate with potassium nitrate has been called toughened silver nitrate, also lunar caustic. When the tip of the applicator is impregnated with this compound, as in ARZOL, the silver nitrate can be applied quickly and conveniently to the precise area to be treated without spread of the escharotic to adjacent healthy tissues.

Exposure to light causes the silver in the tip to oxidize and turn brown in color. This discoloration does not affect the therapeutic action of the tip and the oxidized film readily dissolves when dipped in water.

Moisture has a deteriorating effect on the tip. It may cause it to break or loosen from the applicator; therefore the applicators should be kept in a dry place.

CAUTION: Silver Nitrate is a caustic compound, the improper use of which may cause chemical burns. Silver Nitrate mixes with body fluids; this mixture is caustic and tissue damage may result if not removed quickly. Contact of Silver Nitrate applicators on neonates (as in use on the umbilicus) and on thin delicate skin should be extremely short in duration.

INDICATIONS

INDICATIONS & USAGE SECTION

On the skin, applications of silver nitrate are recommended for cauterization of wounds and sluggish ulcers, also for removal of granulation tissue and warts.

On mucous membranes, silver nitrate may be applied to small ulcers and aphthae in the mouth resulting from injury or stomatitis, to infected tonsils, to rectal fissures and fistulae, and to vaginal or cervical ulcerations or erosions. Epistaxis may be controlled by direct application to the site of hemorrhage within the nostrils.

APPLICATION

DOSAGE & ADMINISTRATION SECTION

ARZOL may be applied direct to mucous membranes and other moist surfaces. In the case of dry skin, the applicator tip should be dipped in water immediately before use. Apply carefully to the area to be treated. DO NOT USE ON THE EYES.

SIDE EFFECTS

WARNINGS SECTION

Silver nitrate blackens the tissues to which it is applied but this discoloration gradually disappears. In the case of applicators, poisoning from ingestion is rare.

ANTIDOTE

OTHER SAFETY INFORMATION

In case of accidental poisoning, follow these directions:

External:

Eye Exposure -- First: Wash out the eye with lukewarm water for at least fifteen (15) minutes then call your physician or go to your nearest Emergency Room.

Skin Exposure -- First: Wash the area very thoroughly with soap and water then call your physician.

Internal:

First: Give one (1) glass of milk or water then call your physician or go to your nearest Emergency Room.

HAZARDS

ADVERSE REACTIONS SECTION

Long continued applications to large areas may produce argyria, a slate-blue discoloration of the skin and mucous membranes.

AVAILABILITY

HOW SUPPLIED SECTION

ARZOL Silver Nitrate Applicators are supplied in boxes of 100 containing 10 packets each with 10 applicators; also, in plastic tubes containing 100 applicators.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Arzol Box PackagingArzol Box Packaging

STATEMENT OF IDENTITY SECTION

Arzol® Silver Nitrate Applicators

DOSAGE FORMS & STRENGTHS SECTION

Silver Nitrate 75%

Potassium Nitrate 25%

DESCRIPTION SECTION

FOR SIMPLIFIED SILVER NITRATE THERAPY

WARNINGS SECTION

POISON

WARNINGS SECTION

CAUTION:

Federal law prohibits dispensing without prescription. Do not open this box or dispense packets or applicators separately.

WARNINGS AND PRECAUTIONS SECTION

WARNING:

Keep out of reach of children. Keep in dry and dark place. Do not use on the eyes.

HOW SUPPLIED SECTION

100 APPLICATORS

ANTIDOTE

OTHER SAFETY INFORMATION

In case of accidental poisoning, follow these directions.

EXTERNAL -

EYE EXPOSURE:

FIRST: Wash out the eye with lukewarm water for at least fifteen (15) minutes

THEN: call your physician or go to your nearest Emergency Room.

SKIN EXPOSURE:

FIRST: Wash the areas very thoroughly with soap and water

THEN: call your physician.

INTERNAL:

FIRST: Give one (1) glass of milk or water

THEN: call your physician or go to your nearest Emergency Room.

STABILITY PRECAUTIONS

STORAGE AND HANDLING SECTION

Light causes the silver in the tip to oxidize and turn brown in color. This does not affect the therapeutic action of the tip and the oxidized film readily dissolves when dipped in water.

Moisture has a deteriorating effect on the tip. It will cause the tip to break or loosen from the applicator; therefore the applicators should be kept in a dry and dark place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Arzol Inner Envelope PackagingArzol Inner Envelope Packaging

STATEMENT OF IDENTITY SECTION

ARZOL® Silver Nitrate Applicators

DOSAGE FORMS & STRENGTHS SECTION

(Silver Nitrate 75%)

(Potassium Nitrate 25%)

DESCRIPTION SECTION

for Simplified Silver Nitrate Therapy

WARNINGS SECTION

POISON

HOW SUPPLIED SECTION

TEN (10) applicators

WARNINGS SECTION

Caution: Federal law prohibits dispensing without prescription. Do not dispense packets or applicators separately.

WARNINGS AND PRECAUTIONS SECTION

Warning: Do not use on the eyes. Keep out of reach of children. Keep in a dry and dark place.

WARNINGS SECTION

NOT FOR RESALE

ANTIDOTE

OTHER SAFETY INFORMATION

In case of accidental poisoning, follow these directions:

External:

Eye Exposure:

First: Wash out the eye with lukewarm water for at least fifteen (15) minutes then call your physician or go to your nearest Emergency Room.

Skin Exposure:

First: Wash the area very thoroughly with soap and water then call your physician.

Internal:

First: Give one (1) glass of milk or water then call your physician or go to your nearest Emergency Room.

Stability Precautions

STORAGE AND HANDLING SECTION

Light causes the silver in the tip to oxidize and turn brown in color. This does not affect the therapeutic action of the tip and the oxidized film readily dissolves when dipped in water. Moisture has a deteriorating effect on the tip. It will cause the tip to break or loosen from the applicator; therefore the applicators should be kept in a dry and dark place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Arzol Vial PackagingArzol Vial Packaging

STATEMENT OF IDENTITY SECTION

ARZOL Silver Nitrate Applicators

DOSAGE FORMS & STRENGTHS SECTION

Silver Nitrate 75%

Potassium Nitrate 25%

DESCRIPTION SECTION

For Simplified Silver Nitrate Therapy

WARNINGS SECTION

Caution: Federal law prohibits dispensing without prescription. Do not open this tube or dispense applicators separately.

WARNINGS AND PRECAUTIONS SECTION

Warning: Do not use on the eyes. Keep out of reach of children. Keep in a dry and dark place.

WARNINGS SECTION

POISON

OTHER SAFETY INFORMATION

In case of accidental poisoning, follow these directions:

ANTIDOTE

External:

Eye Exposure:

First: Wash out the eye with lukewarm water for at least fifteen (15) minutes then call your physician or go to your nearest Emergency Room.

Skin Exposure:

First: Wash the area very thoroughly with soap and water then call your physician.

Internal:

First: Give one (1) glass of milk or water then call your physician or go to your nearest Emergency Room.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1117536potassium nitrate 25 % / silver nitrate 75 % Medicated PadPSN13
1117536potassium nitrate 250 MG/ML / silver nitrate 750 MG/ML Medicated PadSCD13
1117536K+ nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY13
1117536Pot nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY13
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SpongeSY13
1117536potassium nitrate 25 % / silver nitrate 75 % Topical StickSY13
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SwabSY13

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 1281287000011Arzol Envelope Packaging Scan.jpg
Data codeCode 1281287000012Arzol Vial Packaging.jpg

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
12870-0001-1Silver Nitrate Applicators10 in 1 PACKETSTICK1013
12870-0001-1Silver Nitrate Applicators10 in 1 BOXSTICK1013
12870-0001-2Silver Nitrate Applicators100 mg in 1 APPLICATORSTICK10013
12870-0001-2Silver Nitrate Applicators100 in 1 VIALSTICK10013

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
12870-0001-1EA - Each12870-0001c2556e6d-781b-4780-bd52-6a8bd30a980a12015-12-02
12870-0001-2EA - Each12870-000135b75510-733f-4272-8c4d-8cb80209abd512015-12-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZE4
SILVER CATIONACTIVE MOIETY57N7B0K90A4
POTASSIUM NITRATEINACTIVE INGREDIENTRU45X2JN0Z4

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12870-000112870-0001-1, 12870-0001-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM NITRATERU45X2JN0ZACTIB
SILVER NITRATE95IT3W8JZEACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
122024-10-10full-release2026-05-31 21:14:08

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
Silver Nitrate ApplicatorsSILVER NITRATE APPLICATORSArzol Chemical Company23b83457-8cbc-26f1-e054-00144ff8d46c2025-10-29Warnings, Adverse reactionsExact identifier
ndc (package): 12870-0001-2
ndc (package): 12870-0001-1
ndc (product): 12870-0001
ndc11 (package): 12870000102
ndc11 (package): 12870000101
spl id: 424dba13-53c3-5abf-e063-6394a90a4722
spl set id: 23b83457-8cbc-26f1-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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