NDC 43742-1090 Trauma Relief

Chamomilla, Echinacea (angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Bryonia (alba), Calendula Officinalis, Arnica Montana, Bellis Perennis, Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Impatiens Glandulifera, Flos, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Symphytum Officinale, Rhus Tox, Hepar Sulphuris Calcareum, Carbo Vegetabilis

NDC Product Code 43742-1090

NDC CODE: 43742-1090

Proprietary Name: Trauma 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: Chamomilla, Echinacea (angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Bryonia (alba), Calendula Officinalis, Arnica Montana, Bellis Perennis, Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Impatiens Glandulifera, Flos, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Symphytum Officinale, Rhus Tox, Hepar Sulphuris Calcareum, Carbo Vegetabilis 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1090-1

Package Description: 126 g in 1 TUBE

NDC Product Information

Trauma Relief with NDC 43742-1090 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Trauma Relief is chamomilla, echinacea (angustifolia), hamamelis virginiana, hypericum perforatum, millefolium, bryonia (alba), calendula officinalis, arnica montana, bellis perennis, clematis vitalba, flos, helianthemum nummularium, flos, impatiens glandulifera, flos, ornithogalum umbellatum, flos, prunus cerasifera, flos, symphytum officinale, rhus tox, hepar sulphuris calcareum, carbo vegetabilis. The product's dosage form is gel and is administered via topical form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Trauma 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.

  • MATRICARIA RECUTITA 3 [hp_X]/g
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/g
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 3 [hp_X]/g
  • HYPERICUM PERFORATUM 3 [hp_X]/g
  • ACHILLEA MILLEFOLIUM 3 [hp_X]/g
  • BRYONIA ALBA ROOT 4 [hp_X]/g
  • CALENDULA OFFICINALIS FLOWERING TOP 4 [hp_X]/g
  • ARNICA MONTANA 4 [hp_X]/g
  • BELLIS PERENNIS 6 [hp_X]/g
  • CLEMATIS VITALBA FLOWER 6 [hp_X]/g
  • HELIANTHEMUM NUMMULARIUM FLOWER 6 [hp_X]/g
  • IMPATIENS GLANDULIFERA FLOWER 6 [hp_X]/g
  • ORNITHOGALUM UMBELLATUM FLOWERING TOP 6 [hp_X]/g
  • PRUNUS CERASIFERA FLOWER 6 [hp_X]/g
  • COMFREY ROOT 6 [hp_X]/g
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/g
  • CALCIUM SULFIDE 8 [hp_X]/g
  • ACTIVATED CHARCOAL 12 [hp_X]/g

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ARGININE (UNII: 94ZLA3W45F)
  • SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • DEHYDROACETIC ACID (UNII: 2KAG279R6R)
  • GLYCINE (UNII: TE7660XO1C)
  • HYALURONIC ACID (UNII: S270N0TRQY)
  • ASPARTIC ACID (UNII: 30KYC7MIAI)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
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: 11-02-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 08-28-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Trauma 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:

Chamomilla 3X, Echinacea (Angustifolia) 3X, Hamamelis Virginiana 3X, Hypericum Perforatum 3X, Millefolium 3X, 6X, Bryonia (Alba) 4X, Calendula Officinalis 4X, Arnica Montana 4X, 12X, 30X, 200X, Belladonna 6X, Bellis Perennis 6X, Clematis Vitalba, Flos 6X, Helianthemum Nummularium, Flos 6X, Impatiens Glandulifera, Flos 6X, Ornithogalum Umbellatum, Flos 6X, Prunus Cerasifera, Flos 6X, Symphytum Officinale 6X, Rhus Tox 6X, 12X, 30X, Hepar Sulphuris Calcareum 8X, Carbo Vegetabilis 12X.

Homeopathic Indications:

For the temporary relief of strains, sprains, and joint pain.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of strains, sprains, and joint pain.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.If pregnant or breast-feeding, seek advice of a health professional before use.Do not use if seal is broken or missing.For external use only, not for oral use.Do not expose to extreme heat.

Keep Out Of Reach Of Children:

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Suggested Application:

Apply a small amount on the area of discomfort, gently rubbing the gel into the skin. Application should be as soon after the injury as possible. Repeat three times in ten minute intervals; thereafter apply three times daily as needed.

Inactive Ingredients:

Demineralized Water, Glycerin, L-Arginine Base, Sodium PCA, Aloe Barbadensis Leaf Juice, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzylalcohol-DHA, Glycine, Hyaluronic Acid, L-Aspartic Acid.

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1090-1HOMEOPATHICTRAUMA RELIEF GELWith Aloe VeraNET WT 4.44 OZ (126 G)

* Please review the disclaimer below.