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NDC 62795-7007 T-relief Extra Strength Cream

Arnica Montana,Calendula Officinalis Flowering Top,Echinacea Unspecified,Aconitum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62795-7007?
  4. T-relief Extra Strength Cream Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
62795-7007
Proprietary Name:
T-relief Extra Strength Cream
Non-Proprietary Name: [1]
Arnica Montana, Calendula Officinalis Flowering Top, Echinacea Unspecified, Aconitum Napellus, Achillea Millefolium, Hamamelis Virginiana Root Bark Stem Bark, Matricaria Chamomilla, Atropa Belladonna, Bellis Perennis, Ruta Graveolens Flowering Top, Baptisia Tinctoria Root, Comfrey Root And Hypericum Perforatum
Substance Name: [2]
Achillea Millefolium; Aconitum Napellus; Arnica Montana; Atropa Belladonna; Baptisia Tinctoria Root; Bellis Perennis; Calendula Officinalis Flowering Top; Comfrey Root; Echinacea, Unspecified; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum; Matricaria Chamomilla; Ruta Graveolens Flowering Top
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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]
    Medinatura Inc
    Labeler Code:
    62795
    Product Label ID:
    12f6cf2f-a924-42b1-9ca0-c360c7a59244
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-19-2017
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 62795-7007-4

    Package Description: 85 g in 1 TUBE

    NDC Code 62795-7007-5

    Package Description: 227 g in 1 JAR

    NDC Code 62795-7007-6

    Package Description: 1 JAR in 1 CARTON / 227 g in 1 JAR

    NDC Code 62795-7007-7

    Package Description: 1 TUBE in 1 CARTON / 85 g in 1 TUBE

    Product Details

    What is NDC 62795-7007?

    The NDC code 62795-7007 is assigned by the FDA to the product T-relief Extra Strength Cream which is a human over the counter drug product labeled by Medinatura Inc. The generic name of T-relief Extra Strength Cream is arnica montana, calendula officinalis flowering top, echinacea unspecified, aconitum napellus, achillea millefolium, hamamelis virginiana root bark stem bark, matricaria chamomilla, atropa belladonna, bellis perennis, ruta graveolens flowering top, baptisia tinctoria root, comfrey root and hypericum perforatum. The product's dosage form is cream and is administered via topical form. The product is distributed in 4 packages with assigned NDC codes 62795-7007-4 85 g in 1 tube , 62795-7007-5 227 g in 1 jar , 62795-7007-6 1 jar in 1 carton / 227 g in 1 jar, 62795-7007-7 1 tube in 1 carton / 85 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 T-relief Extra Strength Cream?

    Pain Relief

    What are T-relief Extra Strength Cream 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 T-relief Extra Strength Cream UNII Codes?

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

    Which are T-relief Extra Strength Cream 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:

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    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".