NDC 62795-1041 T-relief Extra Strength

Arnica Montana,Calendula Officinalis Flowering,Hamamelis Virginiana Root - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
62795-1041
Proprietary Name:
T-relief Extra Strength
Non-Proprietary Name: [1]
Arnica Montana, Calendula Officinalis Flowering, Hamamelis Virginiana Root Bark/stem, Baptisia Tinctoria Root, Bellis Perennis, Echinacea, Unspecified, Aconitum Napellus, Matricaria Chamomilla, Achillea Millefolium, Atropa Belladonna, Hypericum Perforatum, Ruta Graveolens Flowering Top And Comfrey Root
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:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Medinatura Inc
    Labeler Code:
    62795
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-01-2018
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    Size(s):
    9 MM
    Imprint(s):
    RADIANTMAN
    Score:
    1

    Product Packages

    NDC Code 62795-1041-2

    Package Description: 1 BOTTLE in 1 CARTON / 90 TABLET, CHEWABLE in 1 BOTTLE

    NDC Code 62795-1041-3

    Package Description: 4 TABLET, CHEWABLE in 1 POUCH

    NDC Code 62795-1041-4

    Package Description: 1 BOTTLE in 1 CARTON / 100 TABLET, CHEWABLE in 1 BOTTLE

    NDC Code 62795-1041-5

    Package Description: 250 TABLET, CHEWABLE in 1 BOTTLE

    NDC Code 62795-1041-6

    Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE

    NDC Code 62795-1041-7

    Package Description: 60 TABLET, CHEWABLE in 1 BOTTLE

    Product Details

    What is NDC 62795-1041?

    The NDC code 62795-1041 is assigned by the FDA to the product T-relief Extra Strength which is a human over the counter drug product labeled by Medinatura Inc. The generic name of T-relief Extra Strength is arnica montana, calendula officinalis flowering, hamamelis virginiana root bark/stem, baptisia tinctoria root, bellis perennis, echinacea, unspecified, aconitum napellus, matricaria chamomilla, achillea millefolium, atropa belladonna, hypericum perforatum, ruta graveolens flowering top and comfrey root. The product's dosage form is tablet, chewable and is administered via oral form. The product is distributed in 6 packages with assigned NDC codes 62795-1041-2 1 bottle in 1 carton / 90 tablet, chewable in 1 bottle, 62795-1041-3 4 tablet, chewable in 1 pouch , 62795-1041-4 1 bottle in 1 carton / 100 tablet, chewable in 1 bottle, 62795-1041-5 250 tablet, chewable in 1 bottle , 62795-1041-6 100 tablet, chewable in 1 bottle , 62795-1041-7 60 tablet, chewable in 1 bottle . 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?

    Relieves muscle, Joint, back, nerve and arthritis pain.

    What are T-relief Extra Strength 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 UNII Codes?

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

    Which are T-relief Extra Strength 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".