NDC 62795-1034 T-relief

T-relief

NDC Product Code 62795-1034

NDC CODE: 62795-1034

Proprietary Name: T-relief 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: T-relief 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.

Product Characteristics

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

NDC Code Structure

NDC 62795-1034-2

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

NDC Product Information

T-relief with NDC 62795-1034 is a a human over the counter drug product labeled by Medinatura Inc. The generic name of T-relief is t-relief. The product's dosage form is tablet, chewable and is administered via oral form.

Labeler Name: Medinatura Inc

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.

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 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.

  • ACONITUM NAPELLUS 3 [hp_M]/1
  • MATRICARIA RECUTITA 2 [hp_X]/1
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 2 [hp_X]/1
  • HYPERICUM PERFORATUM 3 [hp_X]/1
  • RUTA GRAVEOLENS FLOWERING TOP 4 [hp_X]/1
  • COMFREY ROOT 8 [hp_X]/1
  • BAPTISIA TINCTORIA ROOT 2 [hp_X]/1
  • ATROPA BELLADONNA 3 [hp_X]/1
  • BELLIS PERENNIS 2 [hp_X]/1
  • CALENDULA OFFICINALIS FLOWERING TOP 2 [hp_X]/1
  • ECHINACEA ANGUSTIFOLIA 2 [hp_X]/1
  • ARNICA MONTANA 3 [hp_X]/1

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.

  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)

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: 12-01-2015 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: 12-31-2020 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’.

* Please review the disclaimer below.

T-relief Product Label Images

T-relief 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

Indications

  • Relieves Pain:Joint PainBack PainMuscular Pain

Warnings

If pregnant or breast-feeding ask a heath 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
™ or any of its ingredients exists

Directions

Adults and children 12 years and older: Chew 2-3 tablets every 4 hours. Do not exceed 12 tablets per 24 hours.
For children under 4 years, consult your health professional.
Allow tablets to dissolve completely in the mouth.

Inactive Ingredients

Lactose and Magnesium Stearate

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Uses

For the temporary relief of minor joint pain, back pain and muscular pain

Active Ingredients

ACONITUM NAPELLUS, MATRICARIA RECUTITA, ARNICA MONTANA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP, COMFREY ROOT, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, and ECHINACEA ANGUSTIFOLIA.

* Please review the disclaimer below.