Label: PAIN RELIEVING FOOT- apis mellifera, pseudognaphalium obtusifolium, gelsemium sempervirens root cream

  • NDC Code(s): 43689-0033-1, 43689-0033-2
  • Packager: The Magni Group Inc
  • 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 November 15, 2022

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

  • Active ingredients

    Gnaphalium polycephalum
    Honeybee (Apis Mellifica)
    Yellow Jessamine (Gelsemium sempervirens)

  • Purpose

    Relieves Foot Pain

    External Analgesic

  • Use

    Temporarily relieves leg and foot pain.

  • Warnings

    ​For external use only.

    Avoid contact with eyes.

  • Do not use

    • On open wounds
    • Cuts
    • Damaged skin
    • Infected skin.

    Stop Use and Ask a Doctor

    If symptoms persist for more than 7 days or worsen.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Generously apply and massage into all surfaces of the feet, heels, and toes twice daily.

    Apply to legs as needed.

    Most beneficial when appied after bathing, showering, or a foot soak.

    There is no scientifica evidence that this product works.

    The product's claims are based on theories of homeophathy from the 1700s tht are not accepted by most medical experts.

  • Inactive ingredients

    Water, canola oil, beeswax, octyl stearate, wintergreen oil, tocopheryl acetate, triethanolamine, oil of bergamot, camphor, menthol, eucalyptus oil, steareth-10, steareth-21, ceteth-20, stearic acid, cetyl alcohol, glyceryl stearate, peg-100, propylene glycol, zanthan gum, methylparaben, propylparaben, carbomer 940, imidazolidinyl urea.

  • Pain Relieving Foot Cream, 113g (43689-0033)

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    PAIN RELIEVING FOOT 
    apis mellifera, pseudognaphalium obtusifolium, gelsemium sempervirens root cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43689-0033
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (PSEUDOGNAPHALIUM OBTUSIFOLIUM - UNII:36XQ854NWW) PSEUDOGNAPHALIUM OBTUSIFOLIUM6 [hp_X]  in 1 g
    APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA3 [hp_X]  in 1 g
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT6 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CANOLA OIL (UNII: 331KBJ17RK)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    OCTYL STEARATE (UNII: 772Y4UFC8B)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    BERGAMOT OIL (UNII: 39W1PKE3JI)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    STEARETH-10 PHOSPHATE (UNII: 0B25H7PFT3)  
    STEARETH-21 (UNII: 53J3F32P58)  
    CETETH-20 PHOSPHATE (UNII: 921FTA1500)  
    STEARIC ACID D7 (UNII: T3B081197X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    IMIDUREA (UNII: M629807ATL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43689-0033-1113 g in 1 JAR; Type 0: Not a Combination Product05/05/2017
    2NDC:43689-0033-21 in 1 BOX05/05/2017
    2113 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/05/2017
    Labeler - The Magni Group Inc (113501902)
    Registrant - United Laboratories Manufacturing, LLC (807878116)
    Establishment
    NameAddressID/FEIBusiness Operations
    United Laboratories Manufacturing, LLC807878116manufacture(43689-0033)