62795-1041 NDC - T-RELIEF EXTRA STRENGTH (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)

Drug Information

  • Product NDC: 62795-1041
  • Proprietary Name: T-Relief Extra Strength
  • Non Proprietary Name: 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
  • Active Ingredient(s): 2 [hp_X]/1 ACHILLEA MILLEFOLIUM; 3 [hp_X]/1 ACONITUM NAPELLUS; 3 [hp_X]/1 ARNICA MONTANA; 3 [hp_X]/1 ATROPA BELLADONNA; 2 [hp_X]/1 BAPTISIA TINCTORIA ROOT; 2 [hp_X]/1 BELLIS PERENNIS; 2 [hp_X]/1 CALENDULA OFFICINALIS FLOWERING TOP; 6 [hp_X]/1 COMFREY ROOT; 2 [hp_X]/1 ECHINACEA, UNSPECIFIED; 2 [hp_X]/1 HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; 3 [hp_X]/1 HYPERICUM PERFORATUM; 2 [hp_X]/1 MATRICARIA CHAMOMILLA; 3 [hp_X]/1 RUTA GRAVEOLENS FLOWERING TOP
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET, CHEWABLE

Labeler Information

Field Name Field Value
Labeler Name: MediNatura Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:2/1/2018

Package Information

No. Package Code Package Description Billing Unit
162795-1041-21 BOTTLE in 1 CARTON (62795-1041-2) / 90 TABLET, CHEWABLE in 1 BOTTLEEA
262795-1041-34 TABLET, CHEWABLE in 1 POUCH (62795-1041-3)
362795-1041-41 BOTTLE in 1 CARTON (62795-1041-4) / 100 TABLET, CHEWABLE in 1 BOTTLEEA
462795-1041-5250 TABLET, CHEWABLE in 1 BOTTLE (62795-1041-5)EA
562795-1041-6100 TABLET, CHEWABLE in 1 BOTTLE (62795-1041-6)
662795-1041-760 TABLET, CHEWABLE in 1 BOTTLE (62795-1041-7)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62795-1041The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMET-Relief Extra StrengthThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEARNICA 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 ROOTThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, CHEWABLEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/1/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEMediNatura IncName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACHILLEA 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 TOPAn 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.
ACTIVE NUMERATOR STRENGTH2; 3; 3; 3; 2; 2; 2; 6; 2; 2; 3; 2; 3 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 

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This page was last updated on: 11/21/2025

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