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 December 13, 2024

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

View All Sections
  • 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 CARTON02/09/201702/01/2024
    130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    2NDC:65121-209-321 in 1 CARTON02/09/201702/01/2024
    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 DrugM01702/06/201402/01/2024
    Labeler - Pure Source, LLC (080354456)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source, LLC080354456manufacture(65121-209)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!