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biochemistry PAIN RELIEF FOOT ACTIVE

Dosage form: liquid
Ingredients: BENZYL ALCOHOL 190mg in 1mL, LIDOCAINE HYDROCHLORIDE 40mg in 1mL
Labeler: Pure Source, LLC
NDC Code: 65121-209

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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 o - 87 o F
  • 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)

BIOCHEMISTRY PAIN RELIEF FOOT ACTIVE 
benzyl alcohol, lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-209
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZYL ALCOHOL (BENZYL ALCOHOL) BENZYL ALCOHOL190 mg  in 1 mL
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
DIMETHYL SULFONE 
GLYCYRRHIZA GLABRA 
POTASSIUM SORBATE 
PEPPERMINT OIL 
PROPYLENE GLYCOL 
TEA TREE OIL 
Packaging
#Item CodePackage Description
1NDC:65121-209-311 BOTTLE, SPRAY in 1 CARTON
130 mL in 1 BOTTLE, SPRAY
2NDC:65121-209-321 BOTTLE, SPRAY in 1 CARTON
260 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/06/2014
Labeler - Pure Source, LLC (080354456)
Establishment
NameAddressID/FEIOperations
Pure Source, LLC080354456manufacture(65121-209), repack(65121-209), relabel(65121-209)

 
Pure Source, LLC

Medically reviewed on Feb 10, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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