Label: TRAUMEEL- arnica montana root, atropa belladonna, calendula officinalis flowering top, matricaria recutita, achillea millefolium, calcium sulfide, comfrey root, aconitum napellus, bellis perennis, mercurius solubilis, hypericum perforatum, echinacea, unspecified, echinacea purpurea and hamamelis virginiana root bark/stem bark injection

  • NDC Code(s): 50114-7004-1, 50114-7004-2
  • Packager: Medinatura
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated October 14, 2021

If you are a consumer or patient please visit this version.

  • Description

    Active Ingredients:

    Ingredient name              Potency            Quantity               Final dilution

    Aconitum napellus                2X               1.32 μl                    5.22X

    Arnica montana, radix          2X               2.20 μl                    5.00X

    Bellis perennis                      2X               1.10 μl                    5.30X

    Belladonna                          2X                2.20 μl                    5.00X

    Calendula officinalis              2X               2.20 μl                    5.00X

    Chamomilla                         3X               2.20 μl                    6.00X

    Echinacea                            2X               0.55 μl                    5.60X

    Echinacea purpurea              2X               0.55 μl                    5.60X

    Hamamelis virginiana           1X                0.22 μl                    5.00X

    Hepar sulphuris calcareum   6X                2.20 μl                    9.00X

    Hypericum perforatum         2X               0.66 μl                    5.52X

    Mercurius solubilis                6X               1.10 μl                    9.30X

    Millefolium                           3X               2.20 μl                    6.00X

    Symphytum officinale          6X               2.20 μl                     9.00X

  • INDICATION AND USAGE

    Treatment of injuries and various conditions of the musculoskeletal system.

    • Traumeel® Injection Solution is a homeopathic drug product indicated for the treatment of injuries, inflammatory and degenerative conditions of the musculoskeletal system and for the relief of associated symptoms such as pain

    Co-administration Therapy with Zeel® Injection Solution for the treatment of inflammatory and degenerative conditions of the musculoskeletal system.

    • Traumeel ® Injection Solution is a homeopathic drug product indicated, in combination with Zeel® Injection Solution, for the treatment of inflammatory and degenerative conditions of the musculoskeletal system, such as arthrosis/osteoarthritis and/or rheumatic joint diseases, and for the relief of symptoms including pain, swelling, and joint stiffness.

  • DOSAGE AND ADMINISTRATION

    General Considerations

    • The dosage schedules listed below can be used as a general guide for the administration of Traumeel® Injection Solution.
    • If co-administration with a local anesthetic is desired, Traumeel® Injection Solution may be mixed with lidocaine or similar agents at the discretion of the physician.

    • Traumeel® Injection Solution may be administered s.c., i.d., i.m., i.a. or i.v.
    • The interval between injections is left to the discretion of the HCP, but should not exceed 1 ampule in 24 hours.
    • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Draw up the contents of the ampule into the syringe. Discard half or one third of the contents, depending on the required dosage, before administering.
    • Only licensed practitioners with sufficient expertise in injecting drugs, including the respective route of

      administration, should administer the product.

    Standard Dosage - for the treatment of injuries, inflammatory and degenerative conditions of the musculoskeletal system and for the relief of associated symptoms such as pain.

    Adults and children 12 years and older:

    1 ampule 1 to 3 times per 7 days

    Children 6 to 11 years:

    2/3 of an ampule 1 to 3 times per 7 days

    Children 2 to 5 years:

    1/2 ampule 1 to 3 times per 7 days

    Acute Dosage - for the treatment of injuries, inflammatory and degenerative conditions of the musculoskeletal system and for the relief of associated symptoms such as pain.

    Adults and children 12 years and older:

    1 ampule daily, and then continue with standard dosage

    Children 6 to 11 years:

    2/3 of an ampule daily, and then continue with standard dosage

    Children 2 to 5 years:

    1/2 ampule daily, and then continue with standard dosage

    Co-administration therapy with Zeel® Injection Solution - for the treatment of inflammatory and degenerative conditions of the musculoskeletal system, such as arthrosis/osteoarthritis and/or rheumatic joint diseases, and for the relief of symptoms including pain, swelling, and joint stiffness.

    • In the treatment of musculoskeletal conditions, if co-administration with another homeopathic medicinal product is desired, Traumeel® Injection Solution may be mixed in a ratio of 1:1 with Zeel® Injection Solution.
    • For convenience, the daily dose of Traumeel® Injection Solution may be administered at the same time as a Zeel® Injection Solution, according to the dosing recommendations for each medication.

  • CONTRAINDICATIONS

    • Traumeel® Injection Solution is contraindicated in patients with known hypersensitivity to Traumeel® or any of its ingredients.

  • WARNINGS AND PRECAUTIONS

    None

  • ADVERSE REACTIONS


    Post-marketing Experience

    • The following adverse events have been identified during post-marketing use of Traumeel® Injection Solution. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    • Adverse event rates observed in Monotherapy use of Traumeel® Injection Solution: Allergic (hypersensitivity) reactions (e.g. skin allergies, redness/swelling at the injection site, even up to anaphylaxis) may occur in isolated cases.

    • Adverse event rates observed in the Monotherapy use of Zeel® Injection Solution: Allergic (hypersensitivity) skin reactions may occur in isolated cases.

    •To report SUSPECTED ADVERSE REACTIONS, contact MediNatura at 1.844.633.4628 or info@medinatura.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

  • OVERDOSAGE

    No negative effects of an overdose have been reported and none are expected due to the homeopathic dilutions.

  • CLINICAL PHARMACOLOGY

    Mechanism of Action

    The exact mechanism of Traumeel® Injection Solution is not fully understood.

    Pharmacodynamics

    Not applicable for homeopathic medicinal products.

  • DOSAGE

    One ampule containing 2.2 ml each containing the active ingredients in the strengths listed under Description.

  • PRINCIPAL DISPLAY PANEL

    Traumeel 2.2ml Injection.jpg

  • INGREDIENTS AND APPEARANCE
    TRAUMEEL 
    arnica montana root, atropa belladonna, calendula officinalis flowering top, matricaria recutita, achillea millefolium, calcium sulfide, comfrey root, aconitum napellus, bellis perennis, mercurius solubilis, hypericum perforatum, echinacea, unspecified, echinacea purpurea and hamamelis virginiana root bark/stem bark injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:50114-7004
    Route of AdministrationINTRADERMAL, INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS, INTRA-ARTICULAR
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT2 [hp_X]  in 2.2 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA2 [hp_X]  in 2.2 mL
    CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP2 [hp_X]  in 2.2 mL
    MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA3 [hp_X]  in 2.2 mL
    ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK) ACHILLEA MILLEFOLIUM3 [hp_X]  in 2.2 mL
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE6 [hp_X]  in 2.2 mL
    COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT6 [hp_X]  in 2.2 mL
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS2 [hp_X]  in 2.2 mL
    BELLIS PERENNIS (UNII: 2HU33I03UY) (BELLIS PERENNIS - UNII:2HU33I03UY) BELLIS PERENNIS2 [hp_X]  in 2.2 mL
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS6 [hp_X]  in 2.2 mL
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM2 [hp_X]  in 2.2 mL
    ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX) ECHINACEA, UNSPECIFIED2 [hp_X]  in 2.2 mL
    ECHINACEA PURPUREA (UNII: QI7G114Y98) (ECHINACEA PURPUREA - UNII:QI7G114Y98) ECHINACEA PURPUREA2 [hp_X]  in 2.2 mL
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK1 [hp_X]  in 2.2 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50114-7004-110 in 1 CARTON05/09/200712/31/2024
    12.2 mL in 1 AMPULE; Type 0: Not a Combination Product
    2NDC:50114-7004-23 in 1 CARTON05/09/200712/31/2024
    22.2 mL in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/09/200712/31/2024
    Labeler - Medinatura (102783016)
    Establishment
    NameAddressID/FEIBusiness Operations
    Biologische Heilmittel Heel315635359manufacture(50114-7004)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hameln Pharma GmbH315869123manufacture(50114-7004)