NDC 62795-1029 T Relief

NDC Product Code 62795-1029

NDC 62795-1029-2

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

T Relief with NDC 62795-1029 is a product labeled by Medinatura Inc. The generic name of T Relief is . The product's dosage form is and is administered via form.

Labeler Name: Medinatura Inc

Dosage Form: -

Product Type: 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.

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 (UNII: J2B2A4N98G)

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
Start Marketing Date: 09-01-2014 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: 12-31-2017 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: I 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

Active Ingredients

*Aconitum napellus 3X, *Arnica montana, radix 3X, *Arnica montana, radix 6X, *Arnica montana, radix 10X, *Baptisia tinctoria 2X, *Belladonna 3X, *Bellis perennis 2X, *Calendula officinalis 2X, *Chamomilla 2X, *Echinacea 2X, *Hamamelis virginiana 2X, *Hypericum perforatum 3X, *Millefolium 2X, *Ruta graveolens 4X, *Symphytum officinale 8X*Natural Ingredients

Inactive Ingredients

Lactose Magnesium stearate

Indications

  • Relievesjoint painback painmuscular pain

Keep Out Of Reach Of Children

Keep out of reach of children

Purpose

For the temporary relief of minor: Joint pain, Back pain, Muscular pain

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 shoul be consulted.
Do not use if known sensitivity to T-Relief™ or any of its ingredients exists.

Dosage And Administration

Adults and children 12 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dose. Do not exceed 12 tablets in 24 hours.
Children 4 to 11 years: 1 tablet every 1/2 to 1 hour, until symptoms lessen, then continue with standard dosage. Do not exceed 8 tablets in 24 hours.
Standard Dosage: Adults and children 12 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours.
Children 4 to 11 years: 2 tablets per day, taking 1 tablet every 6 to 8 hours.
For children under 4 years, consult your health professional.
Allow tablets to dissolve completely in the mouth, do not swallow.

* Please review the disclaimer below.