NDC 62795-9487 Traumeel

Aconitum Napellus, Arnica Montana Root, Atropa Belladonna, Bellis Perennis, Calendula Officinalis Flowering Top, Matricaria Recutita, Echinacea, Unspecified, Echinacea Purpurea, Hamamelis Virginiana Root Bark/stem Bark, Calcium Sulfide, Hypericum Perforatum, Mercurius Solubilis, Achillea Millefolium And Comfrey Root

NDC Product Code 62795-9487

NDC CODE: 62795-9487

Proprietary Name: Traumeel 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: Aconitum Napellus, Arnica Montana Root, Atropa Belladonna, Bellis Perennis, Calendula Officinalis Flowering Top, Matricaria Recutita, Echinacea, Unspecified, Echinacea Purpurea, Hamamelis Virginiana Root Bark/stem Bark, Calcium Sulfide, Hypericum Perforatum, Mercurius Solubilis, Achillea Millefolium And Comfrey Root 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.

NDC Code Structure

NDC 62795-9487-8

Package Description: 1 TUBE in 1 CARTON > 100 g in 1 TUBE

NDC Product Information

Traumeel with NDC 62795-9487 is a a human over the counter drug product labeled by Medinatura Inc. The generic name of Traumeel is aconitum napellus, arnica montana root, atropa belladonna, bellis perennis, calendula officinalis flowering top, matricaria recutita, echinacea, unspecified, echinacea purpurea, hamamelis virginiana root bark/stem bark, calcium sulfide, hypericum perforatum, mercurius solubilis, achillea millefolium and comfrey root. The product's dosage form is ointment and is administered via topical form.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Traumeel 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.


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.

  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • MINERAL OIL (UNII: T5L8T28FGP)

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.

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: 12-14-2021 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: 12-31-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Traumeel Product Label Images

Traumeel 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

Active ingredients: Each 100 g contains:*Aconitum napellus 1X 0.050g; *Arnica montana, radix 3X 1.50g; *Belladonna 1X 0.050g; *Bellis perennis MT 0.100g; *Calendula officinalis MT 0.450g; *Chamomilla MT 0.150g; *Echinacea MT 0.150g; *Echinacea purpurea MT 0.150g; *Hamamelis virginiana MT 0.450g; Hepar sulphuris calcareum 6X 0.025g; *Hypericum perforatum 6X 0.090g; Mercurius solubilis 6X 0.040g; *Millefolium MT 0.090g; *Symphytum officinale 4X 0.100g.*Natural Ingredients

Purpose

Analgesic

Warning

Warnings: For external use only. Cetylstearyl alcohol may cause local skin reactions, i.e.contact dermatitis. Do not apply over large areas of the body. Do not apply over open wounds orbroken skin. If symptoms persist or worsen, or if a rash develops, a physician should be consulted.Do not use if known sensitivity to Traumeel® ointment or any of its ingredients exists. Keep out ofreach of children. If swallowed, get medical help or contact a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.

Directions

Directions: Adults and children 4 years and older: Apply generously to affected areas 2 to 3 times daily, or as directedby your health professional. Massage thoroughly into skin. Traumeel® may be applied using mild compression bandagingand/or occlusive bandaging. For children under 4, use as directed by your health professional.

Inactive Ingredients

Inactive ingredients:Paraffin, liquid, Cetostearyl alcohol (type A), emulsifying, Paraffin, white soft, Ethanol (96 per cent)

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications

For the temporary relief of muscular pain from sports injuries, bruising.

* Please review the disclaimer below.