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NDC 73763-466 Sanitect Antibacterial Hand

Benzalkonium Chloride Soap Soap Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73763-466?
  4. Sanitect Antibacterial Hand Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
73763-466
Proprietary Name:
Sanitect Antibacterial Hand
Non-Proprietary Name: [1]
Benzalkonium Chloride Soap
Substance Name: [2]
Benzalkonium Chloride
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
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]
    Aquagenics Technologies
    Labeler Code:
    73763
    Product Label ID:
    a203e36d-f22e-cb45-e053-2a95a90a7188
    FDA Application Number: [6]
    part333E
    Marketing Category: [8]
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date: [9]
    03-16-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 73763-466-01

    Package Description: 236 mL in 1 BOTTLE, DISPENSING

    NDC Code 73763-466-02

    Package Description: 473 mL in 1 BOTTLE, DISPENSING

    NDC Code 73763-466-03

    Package Description: 946 mL in 1 BOTTLE, DISPENSING

    NDC Code 73763-466-04

    Package Description: 1892 mL in 1 BOTTLE, DISPENSING

    NDC Code 73763-466-05

    Package Description: 3784 mL in 1 BOTTLE, DISPENSING

    Product Details

    What is NDC 73763-466?

    The NDC code 73763-466 is assigned by the FDA to the product Sanitect Antibacterial Hand which is a human over the counter drug product labeled by Aquagenics Technologies. The generic name of Sanitect Antibacterial Hand is benzalkonium chloride soap. The product's dosage form is soap and is administered via topical form. The product is distributed in 5 packages with assigned NDC codes 73763-466-01 236 ml in 1 bottle, dispensing , 73763-466-02 473 ml in 1 bottle, dispensing , 73763-466-03 946 ml in 1 bottle, dispensing , 73763-466-04 1892 ml in 1 bottle, dispensing , 73763-466-05 3784 ml in 1 bottle, dispensing . 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 Sanitect Antibacterial Hand?

    Pump onto wet hands, vigorously work into a lather and rinse thoroughly.

    What are Sanitect Antibacterial Hand 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.

    Which are Sanitect Antibacterial Hand UNII Codes?

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

    Which are Sanitect Antibacterial Hand 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 Sanitect Antibacterial Hand?

    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: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
    • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
    • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap

    * 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.

    [6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

    [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".