43742-1333 NDC - TRAUMA RELIEF (CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, HYPERICUM PERFORATUM, MILLEFOLIUM, CALENDULA OFFICINALIS, ARNICA MONTANA, BELLADONNA, BELLIS PERENNIS, CLEMATIS VITALBA, FLOS, HELIANTHEMUM NUMMULARIUM, FLOS, IMPATIENS GLANDULIFERA, FLOS, ORNITHOGALUM UMBELLATUM, FLOS, PRUNUS CERASIFERA, FLOS, SYMPHYTUM OFFICINALE, RHUS TOX, BRYONIA (ALBA), HEPAR SULPHURIS CALCAREUM, CARBO VEGETABILIS)

Drug Information

  • Product NDC: 43742-1333
  • Proprietary Name: Trauma Relief
  • Non Proprietary Name: Chamomilla, Echinacea (Angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Calendula Officinalis, Arnica Montana, Belladonna, Bellis Perennis, Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Impatiens Glandulifera, Flos, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Symphytum Officinale, Rhus Tox, Bryonia (Alba), Hepar Sulphuris Calcareum, Carbo Vegetabilis
  • Active Ingredient(s): 3 [hp_X]/g ACHILLEA MILLEFOLIUM WHOLE; 12 [hp_X]/g ACTIVATED CHARCOAL; 4 [hp_X]/g ARNICA MONTANA WHOLE; 6 [hp_X]/g ATROPA BELLADONNA; 6 [hp_X]/g BELLIS PERENNIS WHOLE; 8 [hp_X]/g BRYONIA ALBA ROOT; 8 [hp_X]/g CALCIUM SULFIDE; 4 [hp_X]/g CALENDULA OFFICINALIS FLOWERING TOP; 6 [hp_X]/g COMFREY ROOT; 3 [hp_X]/g ECHINACEA ANGUSTIFOLIA WHOLE; 3 [hp_X]/g HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; 6 [hp_X]/g HELIANTHEMUM NUMMULARIUM FLOWER; 3 [hp_X]/g HYPERICUM PERFORATUM WHOLE; 6 [hp_X]/g IMPATIENS GLANDULIFERA FLOWER; 3 [hp_X]/g MATRICARIA CHAMOMILLA WHOLE; 6 [hp_X]/g ORNITHOGALUM UMBELLATUM FLOWERING TOP; 6 [hp_X]/g PRUNUS CERASIFERA FLOWER; 6 [hp_X]/g TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): TOPICAL
  • Dosage Form(s): LIQUID

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/7/2018

Package Information

No. Package Code Package Description Billing Unit
143742-1333-1126 g in 1 BOTTLE, PUMP (43742-1333-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1333The 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 NAMETrauma ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEChamomilla, Echinacea (Angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Calendula Officinalis, Arnica Montana, Belladonna, Bellis Perennis, Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Impatiens Glandulifera, Flos, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Symphytum Officinale, Rhus Tox, Bryonia (Alba), Hepar Sulphuris Calcareum, Carbo VegetabilisThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/7/2018This 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 NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACHILLEA MILLEFOLIUM WHOLE; ACTIVATED CHARCOAL; ARNICA MONTANA WHOLE; ATROPA BELLADONNA; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; COMFREY ROOT; ECHINACEA ANGUSTIFOLIA WHOLE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HELIANTHEMUM NUMMULARIUM FLOWER; HYPERICUM PERFORATUM WHOLE; IMPATIENS GLANDULIFERA FLOWER; MATRICARIA CHAMOMILLA WHOLE; ORNITHOGALUM UMBELLATUM FLOWERING TOP; PRUNUS CERASIFERA FLOWER; TOXICODENDRON PUBESCENS LEAFAn 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 STRENGTH3; 12; 4; 6; 6; 8; 8; 4; 6; 3; 3; 6; 3; 6; 3; 6; 6; 6 
ACTIVE INGRED UNIT[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g 

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This page was last updated on: 12/6/2025

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