SILVER NITRATE APPLICATORS stick
Silver Nitrate Applicators by
Drug Labeling and Warnings
Silver Nitrate Applicators by is a Prescription medication manufactured, distributed, or labeled by Arzol Chemical Company. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
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INSTRUCTIONS FOR USE
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
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
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
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
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
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.
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PRINCIPAL DISPLAY PANEL
CAUTION:
Federal law prohibits dispensing without prescription. Do not open this box or dispense packets or applicators separately.
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.
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PRINCIPAL DISPLAY PANEL
Caution: Federal law prohibits dispensing without prescription. Do not dispense packets or applicators separately.
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.
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PRINCIPAL DISPLAY PANEL
Caution: Federal law prohibits dispensing without prescription. Do not open this tube or dispense applicators separately.
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.
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INGREDIENTS AND APPEARANCE
SILVER NITRATE APPLICATORS
silver nitrate applicators stickProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC: 12870-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE 25 mg in 100 mg SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 75 mg in 100 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 12870-0001-1 10 in 1 BOX 01/01/1937 1 10 in 1 PACKET 1 100 mg in 1 APPLICATOR; Type 0: Not a Combination Product 2 NDC: 12870-0001-2 100 in 1 VIAL 01/01/1937 2 100 mg in 1 APPLICATOR; Type 0: Not a Combination Product 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 Business Operations Arzol Chemical Company 002012128 manufacture(12870-0001)
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