NDC 62795-2010 T-relief Extra Strength

T-relief Extra Strength with NDC 62795-2010 is a 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.

Labeler Name: Medinatura Inc

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.

• CALENDULA OFFICINALIS FLOWERING TOP 2 [hp_X]/50mL
• MATRICARIA RECUTITA 2 [hp_X]/50mL
• HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 3 [hp_X]/50mL
• ACHILLEA MILLEFOLIUM 2 [hp_X]/50mL
• RUTA GRAVEOLENS FLOWERING TOP 3 [hp_X]/50mL
• COMFREY ROOT 8 [hp_X]/50mL
• ACONITUM NAPELLUS 3 [hp_X]/50mL
• ECHINACEA, UNSPECIFIED 2 [hp_X]/50mL
• BAPTISIA TINCTORIA ROOT 2 [hp_X]/50mL
• ATROPA BELLADONNA 3 [hp_X]/50mL
• ARNICA MONTANA 3 [hp_X]/50mL
• BELLIS PERENNIS 2 [hp_X]/50mL
• HYPERICUM PERFORATUM 3 [hp_X]/50mL

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: 12-31-2021 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 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. Values = ‘Y’ or ‘N’.

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