BIOCHEMISTRY PAIN RELIEF FOOT ACTIVE- benzyl alcohol, lidocaine hydrochloride liquid 
Pure Source, LLC

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biochemistry PAIN RELIEF FOOT SPRAY ACTIVE

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

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)

Revised: 12/2024
 
Pure Source, LLC