NDC 62795-2010 T-relief Extra Strength

Calendula Officinalis Flowering Top, Matricaria Recutita, Hamamelis Virginiana Root Bark/stem Bark, Achillea Millefolium, Ruta Graveolens Flowering Top, Comfrey Root, Aconitum Napellus, Echinacea, Unspecified, Baptisia Tinctoria Root, Atropa Belladonna, Arnica Montana, Bellis Perennis And Hypericum Perforatum Solution/ Drops Oral

  1. Labeler Index
  2. Medinatura Inc
  3. NDC: 62795-2010 T-relief Extra Strength

NDC Product Code 62795-2010

NDC CODE: 62795-2010

Proprietary Name: T-relief Extra Strength What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Calendula Officinalis Flowering Top, Matricaria Recutita, Hamamelis Virginiana Root Bark/stem Bark, Achillea Millefolium, Ruta Graveolens Flowering Top, Comfrey Root, Aconitum Napellus, Echinacea, Unspecified, Baptisia Tinctoria Root, Atropa Belladonna, Arnica Montana, Bellis Perennis And Hypericum Perforatum 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as relieves• joint pain• back pain• muscular pain

NDC Code Structure

NDC 62795-2010-4

Package Description: 1 BOTTLE in 1 CARTON > 50 mL in 1 BOTTLE

NDC Product Information

T-relief Extra Strength with NDC 62795-2010 is a human over the counter drug product labeled by Medinatura Inc. The generic name of T-relief Extra Strength is calendula officinalis flowering top, matricaria recutita, hamamelis virginiana root bark/stem bark, achillea millefolium, ruta graveolens flowering top, comfrey root, aconitum napellus, echinacea, unspecified, baptisia tinctoria root, atropa belladonna, arnica montana, bellis perennis and hypericum perforatum. The product's dosage form is solution/ drops and is administered via oral form.

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Product Type: Human Otc Drug 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.

T-relief Extra Strength Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Medinatura Inc
Labeler Code: 62795
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.
Start Marketing Date: 11-05-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2022 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.
Exclude Flag: N - NO 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".

* Please review the disclaimer below.

T-relief Extra Strength Product Label Images

T-relief Extra Strength Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Warnings

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted . Do not use if known sensitivity to T-Relief TM or any of its ingredients exists.

Uses

UsesFor the temporary relief of minor: Muscular Pain, Joint Pain, Back Pain, Nerve Pain and Arthritis Pain.

Keep Out Of Reach Of Children

If symptoms persist or worsen, a health professional should be consulted .

Purpose

Relieves• Joint Pain• Back Pain• Muscular Pain

Directions

Adults and children 12 years and older: 10 drops every 4 hours not exceed 60 drops per 24 hours. For children under 12 years: Consult your health professional.

Inactive Ingredients

Ethanol, Purified water

Active Ingredients

Each 50mL contains: *Arnica montana 3X 42%,Wild-Harvested Baptisia tinctoria 2X 9%, *Aconitum napellus 3X 7.5%,*Symphytum officinale 8X 7.5%, Organic Millefolium 2X 6%, *Rutagraveolens 3X 4%, *Arnica montana 4X 3.6%, *Arnica montana 8X 3.6%,*Bellis perennis 2X 3%, Organic Calendula officinalis 2X 3%, OrganicEchinacea 2X 3%, *Hamamelis virginiana 2X 3%, *Hypericum perforatum3X 3%, *Belladonna 3X 0.9%, Organic Chamomilla 2X 0.9%

* Please review the disclaimer below.