Label: TRANZGEL- echinacea angustifolia, echinacea purpurea, aconitum napellus, arnica montana, calendula officianalis, hamamelis virginiana, belladonna, bellis perennis, chamomillia, millefolium, hypericum perforatum, symphytum officinale, colchicinum gel

  • 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 September 29, 2010

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

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:

    ECHINACEA ANGUSTIFOLIA 1X HPUS, ECHINACEA PUPUREA 1X HPUS, ACONITUM NAPELLUS 3X HPUS, ARNICA MONTANA 3X HPUS, CALENDULA OFFICIANALIS 1X HPUS, HAMAMELIS VIRGINIANA 1X  HPUS, BELLADONNA 3X HPUS, BELLIS PERENNIS 1X HPUS, CHAMOMILLA 1X HPUS, MILLEFOLIUM 1X HPUS, HYPERICUM PERFORATUM 6X HPUS, SYMPHYTUM OFFICINALE 4X HPUS, COLCHICINUM 3X HPUS

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:

    PURIFIED WATER, ISOPROPYL MYRISTATE, LECITHIN, UREA, DOCUSATE SODIUM, SODIUM HYDROXIDE

  • PRINCIPAL DISPLAY PANEL

    NDC 35781-0194-5

    TRANZGEL

    HOMEOPATHIC TRANSDERMAL PAIN RELIEF GEL

    RX ONLY NET CONTENTS 1.7 FL OZ (50 ML)

    GENSCO LABORATORIES, LLC

    FOR COMPLETE PRESCRIBING INFORMATION, SEE PACKAGE INSERT. STORE AT ROOM TEMPERATURE.


    MANUFACTURED BY FORMULATED SOLUTIONS

    CLEARWATER, FL 33760

    US PATENT #5,654,337



    MANUFACTURED FOR GENSCO LABORATORIES, LLC

    INVERNESS, FL 34452

    352.726.6284

    866.608.6284

    WWW.TRANZGEL.COM

  • PRINCIPAL DISPLAY PANEL

    TRANZ GEL

    HOMEOPATHIC TRANSDERMAL PAIN RELIEF GEL

    RX ONLY NET CONTENTS 1.7 FL OZ (50 ML)

    GENSCO LABORATORIES


  • SPL UNCLASSIFIED SECTION

    MANUFACTURED BY

    FORMULATED SOLUTIONS, LLC

    CLEARWATER FL 33760

    US PATENT #5,654,337



    MANUFACTURED BY

    GENSCO LABORATORIES, LLC

    INVERNESS, FL 34452

    352.726.6284

    866.608.6284

    WWW.TRANZGEL.COM


  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:

    ECHINACEA ANGUSTIFOLIA 1X HPUS, ECHINACEA PUPUREA 1X HPUS, ACONITUM NAPELLUS 3X HPUS, ARNICA MONTANA 3X HPUS, CALENDULA OFFICIANALIS 1X HPUS, HAMAMELIS VIRGINIANA 1X  HPUS, BELLADONNA 3X HPUS, BELLIS PERENNIS 1X HPUS, CHAMOMILLA 1X HPUS, MILLEFOLIUM 1X HPUS, HYPERICUM PERFORATUM 6X HPUS, SYMPHYTUM OFFICINALE 4X HPUS, COLCHICINUM 3X HPUS

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:

    PURIFIED WATER, ISOPROPYL MYRISTATE, LECITHIN, UREA, DOCUSATE SODIUM, SODIUM HYDROXIDE

  • SPL UNCLASSIFIED SECTION

    For complete prescribing information, see package insert. Store at room temperature.

  • DESCRIPTION

    DESCRIPTION

    A homeopathic topical analgesic gel that contains the active ingredients indicated below in the corresponding concentrations.

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:

    50 PARTS EACH: ECHINACEA ANGUSTIFOLIA 1X HPUS, ECHINACEA PUPUREA 1X HPUS, 30 PARTS: ACONITUM NAPELLUS 3X HPUS, 15 PARTS EACH: ARNICA MONTANA 3X HPUS, CALENDULA OFFICIANALIS 1X HPUS, HAMAMELIS VIRGINIANA 1X  HPUS, 10 PARTS: BELLADONNA 3X HPUS, 5 PARTS EACH: BELLIS PERENNIS 1X HPUS, CHAMOMILLA 1X HPUS, 3 PARTS MILLEFOLIUM 1X HPUS, 1 PART EACH: HYPERICUM PERFORATUM 6X HPUS, SYMPHYTUM OFFICINALE 4X HPUS, .01 PART COLCHICINUM 3X HPUS

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:

    PURIFIED WATER, ISOPROPYL MYRISTATE, LECITHIN, UREA, DOCUSATE SODIUM, SODIUM HYDROXIDE

  • Physical Information

    PHYSICAL INFORMATION

    A clear amber colored, viscous gel with a slight floral smell.

  • CLINICAL PHARMACOLOGY

    CLINICAL PHARMACOLOGY

    According to traditional homeopathic literature and Material Medica, the following ingredients provide the following attributes:



    INGREDIENTS                     COMMON NAME               INDICATIONS

    Arnica Montana                  Mountain arnica               Stimulates healing of injured tissues wounds, contusions, hematomas, neuralgia myalgia, analgesia


    Calendula Officianalis         Calendula                           Inflammation

    Hamamelis Virginiana         Witch-hazel                        Analgesic

    Millefolium                             Yarrow                               Hematomas

    Belladonna                           Banewort                           Inflammation locally

    Aconitum Napellus            Monk's hood                       Neuralgia, rheumatism hemostasis, analgeisa

    Chamomilla                           Chamomile                           Inflammation, nausea

    Colchicinum                        Colchicine                              Inflammation and gout

    Symphytum Officinale      Comfrey                                  Neuropathy, contusions, tendonitis, arthritis

    Bellis Perennis                     Daisy                                    brusing, edema, arthralgia

    Echinacea Angustifolia      Narrow leaf cone flower         Inflammation, myalgia

    Echinacia purpurea            purple cone flower               Inflammation, myalgia

    Hypericum perforatum      st. john's wort                        neuropathic pains




  • INDICATIONS & USAGE

    INDICATIONS AND USAGE

    The drug is indicated for the relief of symptoms, including pain and inflammation associated with arthritis or trauma (such as sprains, strains, dislocations, repetitive/overuse injuries, traumatic, edema, post surgical edema, hematoma, general swelling of joints and soft tissues) to areas such as hand, wrist elbow, shoulder, neck, back, knees, ankles, feet and toes.

  • CONTRAINDICATIONS

    CONTRAINDICATIONS

    This drug should not be used by those sensitive to Arnica or any of the other listed ingredients.

  • WARNINGS AND PRECAUTIONS

    WARNINGS AND PRECAUTIONS

    For external use only. direct patient not to ingest TRANZEL and to avoid contact with they eyes, mucous membranes, wounds, and damaged skin. If a rash develops, patient should discontinue use until rash clears. After the disappearance of rash, patient can try TRANZGEL again on a test area and monitor the site for additional results. If no rash or redness results, then patient can resume use. However, if the rash persists or redevelops, use should be discontinued.

    Direct the patient to keep this product out of reach of children and seek medical help or contact a Poison Control Center immediately if swallowed.

    In the homeopathic concentrations used to make TRANZGEL, there are no known or expected interactions with other drugs or laboratory tests. In addition, the homeopathic concentrations used are below any levels with known or suspected toxicities.

  • OVERDOSAGE

    OVERDOSAGE

    According to toxicology studies, a patient would have to orally ingest a minimum of 22 bottles of TRANZGEL to experience any initial toxic effects.

  • ADVERSE REACTIONS

    ADVERSE REACTIONS

    Rarely, allergic skin reactions may occur. These effects are transient and will clear after a few days.

  • DOSAGE & ADMINISTRATION

    Apply a thin layer (1 drop covers an area of skin 2 inches by 2 inches) to the affected area 3-4 times daily and rub in gently. Applications of less than 3-4 times a day will not produce optimum results. Excess drops may be wiped from the area.

  • HOW SUPPLIED

    Package size: 1.7 fl oz (50 ml) airless pump dispensing bottle

    US PATENT 5,654,337

    NDC 35781-0194-5

  • INFORMATION FOR PATIENTS

    STORE AT ROOM TEMPERATURE

    Manufactured by

    Formulated Solutions, LLC

    Clearwater, FL 33760



    Manufactured for

    Gensco Laboratories, LLC

    Inverness, FL 34452

    352-726-6284

    866-608-6284

    www.tranzgel.com


  • PRINCIPAL DISPLAY PANEL

    tranzgel_bottle_label

  • PRINCIPAL DISPLAY PANEL

    Tranzgel_carton_label

  • INGREDIENTS AND APPEARANCE
    TRANZGEL 
    echinacea angustifolia, echinacea purpurea, aconitum napellus, arnica montana, calendula officianalis, hamamelis virginiana, belladonna, bellis perennis, chamomillia, millefolium, hypericum perforatum, symphytum officinale, colchicinum gel
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:35781-0194
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA1 [hp_X]  in 50 mL
    ECHINACEA PURPUREA (UNII: QI7G114Y98) (ECHINACEA PURPUREA - UNII:QI7G114Y98) ECHINACEA PURPUREA1 [hp_X]  in 50 mL
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS3 [hp_X]  in 50 mL
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA3 [hp_X]  in 50 mL
    CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP1 [hp_X]  in 50 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 50 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA3 [hp_X]  in 50 mL
    BELLIS PERENNIS (UNII: 2HU33I03UY) (BELLIS PERENNIS - UNII:2HU33I03UY) BELLIS PERENNIS1 [hp_X]  in 50 mL
    CHAMOMILE (UNII: FGL3685T2X) (CHAMOMILE - UNII:FGL3685T2X) CHAMOMILE1 [hp_X]  in 50 mL
    ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK) ACHILLEA MILLEFOLIUM1 [hp_X]  in 50 mL
    HYPERICUM OIL (UNII: OZU2FC70HY) (HYPERICUM OIL - UNII:OZU2FC70HY) HYPERICUM OIL6 [hp_X]  in 50 mL
    COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT4 [hp_X]  in 50 mL
    COLCHICINE (UNII: SML2Y3J35T) (COLCHICINE - UNII:SML2Y3J35T) COLCHICINE3 [hp_X]  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    UREA (UNII: 8W8T17847W)  
    DOCUSATE SODIUM (UNII: F05Q2T2JA0)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:35781-0194-51 in 1 CARTON
    150 mL in 1 BOTTLE, DISPENSING
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/01/2010
    Labeler - Gensco Laboratories, LLC (831042325)
    Establishment
    NameAddressID/FEIBusiness Operations
    Formulated Solutions143266687manufacture