AVOCA FLEXIBLE CAUSTIC APPLICATOR- silver nitrate applicator stick

Avoca Flexible Caustic Applicator by

Drug Labeling and Warnings

Avoca Flexible Caustic Applicator by is a Prescription medication manufactured, distributed, or labeled by Bray Group Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Dosage & Administration

Prior to use, the applicator stick may be bent or shaped to allow easier access to the target area. The medicated end of the applicator should be moistened in clean water and applied to the affected tissue. One applicator is normally sufficient for each application. The strength of the action is controlled by the amount of water used to moisten the tip. The applicator action can be stopped by washing the area with a saline solution (0.9% sodium chloride).

Uses

Caustic applicators are useful for cauterization of skin or mucous membrane and for the removal of granulation tissue, warts and verrucae.

Contraindications & Antidotes

Caustic applicators must not be used for genital warts. Continued application to mucous membranes and open wounds leads to argyria, a bluish-black discoloration of the skin due to depositions of granules of silver compounds in the connective tissues. This condition persists indefinitely or disappears very slowly. Poisoning by oral ingestion is unlikely with the quantities involved, but treatment for poisoning is the immediate ingestion of large amounts of salt water followed by an emetic. Then administer a dose of Epsom Salts followed with milk. Immediately call a physician.

Caution

KEEP OUT OF REACH OF CHILDREN. DO NOT USE ON OR NEAR EYES.

Storage

Store at room temperature in the closed package, in a dry place protected from light. Exposure to light will cause the silver nitrate tip to turn black, but will not affect the product's potency.

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

AVOCA FLEXIBLE CAUSTIC APPLICATOR 
silver nitrate applicator stick

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 65875-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A)	SILVER NITRATE	30 mg  in 40 mg

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM NITRATE (UNII: RU45X2JN0Z)	10 mg  in 40 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65875-101-09	10 in 1 BOX	04/01/1925
1		4000 mg in 1 VIAL; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/1925

Labeler - Bray Group Limited (217504463)

Registrant - Bray Group Limited (217504463)

Establishment
Name	Address	ID/FEI	Business Operations
Bray Group Limited		217504463	manufacture(65875-101)