Label: AVOCA FLEXIBLE CAUSTIC APPLICATOR- silver nitrate applicator stick
- NDC Code(s): 65875-101-09
- Packager: Bray Group Limited
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 19, 2021
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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
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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.
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- Storage
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AVOCA FLEXIBLE CAUSTIC APPLICATOR
silver nitrate applicator stickProduct 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)
