Indications:
For the temporary relief of
muscular pain, joint pain, and pain from
minor sports injuries and bruises.
Traumeel Tablet
FDA Label NDC 62795-9488
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Medinatura Inc for the product Traumeel (NDC 62795-9488). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications:, warnings:, directions:, inactive ingredients:, keep out of reach of children, purpose, active ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings:
If pregnant or breast-feeding,
ask a health professional before use. Keep
out of reach of children. If symptoms persist
or worsen, a healthcare provider should be
consulted. Do not use if known sensitivity to
Traumeel® or any of its ingredients exists
Directions:
Adults and children 4 years
and older: 1-2 tablets 3 times per day or as
directed by a health practitioner. Not to exceed
6 tablets per 24 hours. Children under 4, as
directed by a health professional. Allow to
completely dissolve in the mouth.
Inactive Ingredients:
Lactose, Magnesium sterate
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Purpose
Analgesic
Active Ingredients:
Each 300 g tablet
contains: *Arnica montana, radix 2X 15mg;
*Calendula officinalis 2X 15mg; *Hamamelis
virginiana 2X 15mg; *Bellis perennis 2X 6mg;
*Echinacea 2X 6mg; *Echinacea purpurea 2X 6mg;
*Hypericum perforatum 2X 3mg; *Aconitum
napellus 3X 30mg; *Chamomilla 3X 24mg;
*Millefolium 3X 15mg; *Belladonna 4X 75mg;
Hepar sulphuris calcareum 8X 30mg; Mercurius
solubilis 8X 30mg; *Symphytum officinale 8X 24mg.
*Natural Ingredients
* Please review the disclaimer below.
