NDC 65875-101 Avoca Flexible Caustic Applicator

Silver Nitrate Applicator Stick Topical - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
65875-101
Proprietary Name:
Avoca Flexible Caustic Applicator
Non-Proprietary Name: [1]
Silver Nitrate Applicator
Substance Name: [2]
Silver Nitrate
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Labeler Name: [5]
    Bray Group Limited
    Labeler Code:
    65875
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    04-01-1925
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 65875-101-09

    Package Description: 10 VIAL in 1 BOX / 4000 mg in 1 VIAL

    Product Details

    What is NDC 65875-101?

    The NDC code 65875-101 is assigned by the FDA to the product Avoca Flexible Caustic Applicator which is a human prescription drug product labeled by Bray Group Limited. The generic name of Avoca Flexible Caustic Applicator is silver nitrate applicator. The product's dosage form is stick and is administered via topical form. The product is distributed in a single package with assigned NDC code 65875-101-09 10 vial in 1 box / 4000 mg in 1 vial. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Avoca Flexible Caustic Applicator?

    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.

    What are Avoca Flexible Caustic Applicator Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • SILVER NITRATE 30 mg/40mg - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.

    Which are Avoca Flexible Caustic Applicator UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Avoca Flexible Caustic Applicator Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    What is the NDC to RxNorm Crosswalk for Avoca Flexible Caustic Applicator?

    RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
    • RxCUI: 1117536 - potassium nitrate 25 % / silver nitrate 75 % Medicated Pad
    • RxCUI: 1117536 - potassium nitrate 250 MG/ML / silver nitrate 750 MG/ML Medicated Pad
    • RxCUI: 1117536 - K+ nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated Pad
    • RxCUI: 1117536 - Pot nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated Pad
    • RxCUI: 1117536 - potassium nitrate 25 % / silver nitrate 75 % Topical Sponge

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".