Label: BIOCHEMISTRY PAIN RELIEF FOOT ACTIVE- benzyl alcohol, lidocaine hydrochloride liquid

  • NDC Code(s): 65121-209-31, 65121-209-32
  • Packager: Pure Source, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • biochemistry PAIN RELIEF FOOT SPRAY ACTIVE


  • Active ingredients

    Benzyl Alcohol 19% Lidocaline HCL 4%

    Purpose

    Topical Anesthetic

  • Uses

    • For temporary relief of minor foot pain.
  • Warnings

    For external use only

    Avoid contact with eyes

    • Do not apply to open wounds or damaged skin
    • If pain persists consult a physician. If conditions worsens, or if symptoms persist for more than seven days, or if conditions clear up and occur again within a few days, discontinue use of this product and consult a physician

    Do not use

    in large quantities over raw surfaces or blistered areas

    Consult your doctor

    if any adverse effect or allergy develops

    If pregnant or breast-feeding

    ask a health professional before use

    Keep out of reach of children

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

    • Over 12-years
    • Apply directly to affected area
    • Do not wrap affected area
    • Do not use more than four times per day
  • Other information

    • Store between 58 - 87 F oo
    • Protect from freezing, direct hear or sunlight.
  • Inactive ingredients

    Aqua (Deionized Water), Dimethyl Sulfone (MSM), Glycyrrhiza Glabra (Licorice) Extract, Potassium Sorbate, Peppermint Oil, Propylene Glycol, SD-Alcohol 40B, Tea Tree Oil

  • biochemistry PAIN RELIEF FOOT SPRAY ACTIVE 30ml (65121-209-31) | biochemistry PAIN RELIEF FOOT SPRAY ACTIVE 60ml (65121-209-32)

    bio chemistry Inner 30bio chemistry Outer 30bio chemistry Inner 60bio chemistry Outer 60

  • INGREDIENTS AND APPEARANCE
    BIOCHEMISTRY PAIN RELIEF FOOT ACTIVE 
    benzyl alcohol, lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-209
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL190 mg  in 1 mL
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65121-209-311 in 1 CARTON02/09/2017
    130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    2NDC:65121-209-321 in 1 CARTON02/09/2017
    260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/06/2014
    Labeler - Pure Source, LLC (080354456)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source, LLC080354456manufacture(65121-209)
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