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Silver Nitrate Applicators

Pronunciation

Dosage Form: applicators stick

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

ARZOL® Silver Nitrate Applicators

Arzol® Silver Nitrate Applicators

Silver Nitrate 75%

Potassium Nitrate 25%

FOR SIMPLIFIED SILVER NITRATE THERAPY

POISON

CAUTION:

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

WARNING:

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

100 APPLICATORS

ANTIDOTE

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

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.

ARZOL® Silver Nitrate Applicators

(Silver Nitrate 75%)

(Potassium Nitrate 25%)

for Simplified Silver Nitrate Therapy

POISON

TEN (10) applicators

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

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

NOT FOR RESALE

ANTIDOTE

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

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.

ARZOL Silver Nitrate Applicators

Silver Nitrate 75%

Potassium Nitrate 25%

For Simplified Silver Nitrate Therapy

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

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

POISON

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.

Silver Nitrate Applicators 
Silver Nitrate Applicators stick
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:12870-0001
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SILVER NITRATE (SILVER CATION) SILVER NITRATE 75 mg  in 100 mg
Inactive Ingredients
Ingredient Name Strength
POTASSIUM NITRATE 25 mg  in 100 mg
Packaging
# Item Code Package Description
1 NDC:12870-0001-1 10 PACKET in 1 BOX
1 10 APPLICATOR in 1 PACKET
1 100 mg in 1 APPLICATOR
2 NDC:12870-0001-2 100 APPLICATOR in 1 VIAL
2 100 mg in 1 APPLICATOR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/01/1937
Labeler - Arzol Chemical Company (002012128)
Registrant - Arzol Chemical Company (002012128)
Establishment
Name Address ID/FEI Operations
Arzol Chemical Company 002012128 manufacture(12870-0001)
Revised: 11/2015
 
Arzol Chemical Company



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