Label: NEURAGEN PAIN RELIEF- hypericum, aconitum napellus, lycopodium, phosphorus, rhus toxicodendron gel

  • Category: HUMAN OTC 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 August 16, 2011

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  • INACTIVE INGREDIENT

    bergamot oil, beeswax, ethyl alcohol, eucalyptus oil, geranium oil, lavender oil, sorbitan monopalmitate, tea tree oil

  • DOSAGE & ADMINISTRATION

    Apply a small amount to the affected area as needed.

  • WARNINGS

    • For external use only. 
    • Avoid eye/mouth contact
    • Strong floral aroma
    • Do not use on broken skin.
    • Discontinue use if skin irritation develops

                If condition worsens or if symptoms persist for more than 2 weeks or if you suspect you are diabetic consult a doctor.

  • ACTIVE INGREDIENT

    Aconitum Napellus 12 C, Hypericum perforatum 12 C, Lycopodium clavatum 12 C, Phosphorus 12 C, Rhus toxicodendron 12 C, Secale cornutum 12 C

  • PURPOSE

    Topical analgesic

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

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

  • INDICATIONS & USAGE

    For rapid, temporary relief of the symptoms of pain, including shooting, burning, tingling and stabbing pain in the hands and feet.

  • STORAGE AND HANDLING

    Store at room temperature 59-86 degrees F (15-30 degrees C)

  • QUESTIONS

    Call toll free 1-888-234-7256 or visit www.neuragen.com

  • PRINCIPAL DISPLAY PANEL

    Neuragen Gel Carton

  • INGREDIENTS AND APPEARANCE
    NEURAGEN  PAIN RELIEF
    hypericum, aconitum napellus, lycopodium, phosphorus, rhus toxicodendron gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15377-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM12 [hp_C]  in 8 g
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS12 [hp_C]  in 8 g
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE12 [hp_C]  in 8 g
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS12 [hp_C]  in 8 g
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF12 [hp_C]  in 8 g
    CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (CLAVICEPS PURPUREA SCLEROTIUM - UNII:01G9XEA93N) CLAVICEPS PURPUREA SCLEROTIUM12 [hp_C]  in 8 g
    Inactive Ingredients
    Ingredient NameStrength
    BERGAMOT OIL (UNII: 39W1PKE3JI)  
    ALCOHOL (UNII: 3K9958V90M)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:15377-006-088 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/01/2009
    Labeler - Origin Biomed Inc (206071222)
    Registrant - Origin Biomed Inc (206071222)
    Establishment
    NameAddressID/FEIBusiness Operations
    C Care Co LLC120585950manufacture
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