NDC 43742-1397 Celeragesic

Echinacea (angustifolia),Calendula Officinalis,Hamamelis Virginiana,Echinacea - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43742-1397
Proprietary Name:
Celeragesic
Non-Proprietary Name: [1]
Echinacea (angustifolia), Calendula Officinalis, Hamamelis Virginiana, Echinacea Purpurea, Bellis Perennis, Chamomilla, Hypericum Perforatum, Millefolium, Ledum Palustre, Arnica Montana, Bryonia (alba), Hepar Sulphuris Calcareum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Symphytum Officinale, Rhus Tox, Aconitum Napellus, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis
Substance Name: [2]
Achillea Millefolium Whole; Aconitum Napellus Whole; Arnica Montana Whole; Bellis Perennis Whole; Bryonia Alba Root; Calcium Sulfide; Calendula Officinalis Flowering Top; Comfrey Root; Echinacea Angustifolia Whole; Echinacea Purpurea Whole; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum Whole; Lactic Acid, L-; Matricaria Chamomilla Whole; Nadide; Pantothenic Acid; Rhododendron Tomentosum Leafy Twig; Sus Scrofa Adrenal Gland; Sus Scrofa Umbilical Cord; Toxicodendron Pubescens Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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]
    Deseret Biologicals, Inc.
    Labeler Code:
    43742
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-31-2018
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43742-1397-1

    Package Description: 57 g in 1 TUBE

    Product Details

    What is NDC 43742-1397?

    The NDC code 43742-1397 is assigned by the FDA to the product Celeragesic which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Celeragesic is echinacea (angustifolia), calendula officinalis, hamamelis virginiana, echinacea purpurea, bellis perennis, chamomilla, hypericum perforatum, millefolium, ledum palustre, arnica montana, bryonia (alba), hepar sulphuris calcareum, nadidum, pantothenic acid, sarcolacticum acidum, symphytum officinale, rhus tox, aconitum napellus, funiculus umbilicalis suis, glandula suprarenalis suis. The product's dosage form is gel and is administered via topical form. The product is distributed in a single package with assigned NDC code 43742-1397-1 57 g in 1 tube . 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 Celeragesic?

    For the temporary relief of muscular pain, joint pain, sports injuries and bruising.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. For the temporary relief of muscular pain, joint pain, sports injuries and bruising.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

    What are Celeragesic 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 Celeragesic UNII Codes?

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

    Which are Celeragesic 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".