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

biochemistry PAIN RELIEF FOOT ACTIVE by

Drug Labeling and Warnings

biochemistry PAIN RELIEF FOOT ACTIVE by is a Otc medication manufactured, distributed, or labeled by Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

BIOCHEMISTRY PAIN RELIEF FOOT ACTIVE 
benzyl alcohol, lidocaine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65121-209
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH)	BENZYL ALCOHOL	190 mg  in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65121-209-31	1 in 1 CARTON	02/09/2017
1		30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 65121-209-32	1 in 1 CARTON	02/09/2017
2		60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/06/2014

Labeler - Pure Source, LLC (080354456)

Establishment
Name	Address	ID/FEI	Business Operations
Pure Source, LLC		080354456	manufacture(65121-209) , repack(65121-209) , relabel(65121-209)