Label: MAGNILIFE KNEE PAIN RELIEF GEL- arnica montana flower, toxicodendron pubescens leaf gel

  • NDC Code(s): 62400-0055-1
  • Packager: United Laboratories Manufacturing, LLC
  • 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 February 16, 2022

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  • Drug Facts

  • Active ingredients (in gel)

    Arnica 1X

    Rhus Tox 4X

    Purpose

    Pain reliever

    For joint pain

  • Uses

    Temporary relief from minor aches and pains of sore muscles and joints associated with: • Arthritis • Knee Pain • Strains • Sprains

  • Warnings

    • For external use only 

    Keep out of reach of children

    Stop use and ask a doctor

    • if you experience worsening symptoms or if symptoms last longer than 7 days • Avoid contact with the eyes or mucous membranes • Do not apply to wounds or damaged skin • Wash hands after use

    If pregnant or breastfeeding,

    • ask a health professional before use

  • Directions

    Adults and children 12 years and older, generously apply and massage into affected areas.

  • Other information

    *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

  • Inactive ingredients

    Alcohol, Aloe Barbadensis Leaf Extract, Benzoic Acid, Carbomer, Croton Lechleri Resin Extract, Dimethyl Sulfone, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Menthyl Nicotinate, Phenoxyethanol, Sorbic Acid, Tromethamine, Uncaria Tomentosa Extract, Water (Aqua)

  • Package Labeling:

    LabelLabel2

  • INGREDIENTS AND APPEARANCE
    MAGNILIFE KNEE PAIN RELIEF GEL 
    arnica montana flower, toxicodendron pubescens leaf gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62400-0055
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ) ARNICA MONTANA FLOWER1 [hp_X]  in 1 g
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF4 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CROTON LECHLERI RESIN (UNII: GGG6W25C63)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SORBIC ACID (UNII: X045WJ989B)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    CAT'S CLAW (UNII: 9060PRM18Q)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62400-0055-1113 g in 1 JAR; Type 0: Not a Combination Product02/10/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic02/10/2022
    Labeler - United Laboratories Manufacturing, LLC (807878116)
    Establishment
    NameAddressID/FEIBusiness Operations
    United Laboratories Manufacturing, LLC807878116manufacture(62400-0055) , label(62400-0055) , pack(62400-0055)
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