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  4. NDC Product Code: 52793-700 Ahealon

NDC 52793-700 Ahealon

Arnica Montana,Calendula Officinalis Flowering Top,Echinacea Angustifolia,St. Johns - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52793-700?
  4. Ahealon Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
52793-700
Proprietary Name:
Ahealon
Non-Proprietary Name: [1]
Arnica Montana, Calendula Officinalis Flowering Top, Echinacea Angustifolia, St. Johns Wort, Silver, Sulfur, Allylthiourea And Urtica Urens
Substance Name: [2]
Allylthiourea; Arnica Montana; Calendula Officinalis Flowering Top; Echinacea Angustifolia; Silver; St. John's Wort; Sulfur; Urtica Urens
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
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]
    Princeton Biotechnology Corporation
    Labeler Code:
    52793
    Product Label ID:
    6720fab5-6ef0-e922-0c2c-2fe5280838ab
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    04-09-2012
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 52793-700-02

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 60 mL in 1 BOTTLE, SPRAY

    NDC Code 52793-700-06

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 6 mL in 1 BOTTLE, SPRAY

    NDC Code 52793-700-10

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 10 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 52793-700?

    The NDC code 52793-700 is assigned by the FDA to the product Ahealon which is a human prescription drug product labeled by Princeton Biotechnology Corporation. The generic name of Ahealon is arnica montana, calendula officinalis flowering top, echinacea angustifolia, st. johns wort, silver, sulfur, allylthiourea and urtica urens. The product's dosage form is spray and is administered via topical form. The product is distributed in 3 packages with assigned NDC codes 52793-700-02 1 bottle, spray in 1 carton / 60 ml in 1 bottle, spray, 52793-700-06 1 bottle, spray in 1 carton / 6 ml in 1 bottle, spray, 52793-700-10 1 bottle, spray in 1 carton / 10 ml in 1 bottle, spray. 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 Ahealon?

    AHEALON is indicated for the acute and chronic treatment of pain and or inflammation, as well as a general healing aid, an infection deterrent, an agent to help reduce scar tissue and a source of moisturization (dry/cracked/burned skin), that include: all burn injuries, radiation dermatitis, surgical incisions, rashes, pruritic conditions, arthritis/joint pain, lower back pain, wounds, pressure sores, tumors, neuropathic discomfort and any generally painful and or inflamed area. Pain remediation can secondarily benefit sleep quality and duration; pain reduction can also relieve chronic stress induced Cortisol production and thus contribute to less patient stress and anxiety and the reversal of chronic non-healing wounds. Expedited use on pain/trauma patients may quickly control pain such as to reduce the possibility of shock.

    What are Ahealon 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 Ahealon UNII Codes?

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

    Which are Ahealon 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:

    * 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".