biochemistry PAIN RELIEF FOOT ACTIVE description, usages, side effects, indications, overdosage, supplying and lots more!

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biochemistry PAIN RELIEF FOOT ACTIVE

Pure Source, Inc.

biochemistry PAIN RELIEF FOOT SPRAY ACTIVE


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

biochemistry PAIN RELIEF FOOT SPRAY ACTIVE


Active ingredients

Benzyl Alcohol 19%
Lidocaline HCL 4%

Purpose

Topical Anesthetic

biochemistry PAIN RELIEF FOOT ACTIVE 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

biochemistry PAIN RELIEF FOOT ACTIVE Other information

  • Store between 58o - 87o 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 biochemistry PAIN RELIEF FOOT ACTIVE biochemistry PAIN RELIEF FOOT ACTIVE biochemistry PAIN RELIEF FOOT ACTIVE

biochemistry PAIN RELIEF FOOT ACTIVE

BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65121-209
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZYL ALCOHOL 190 mg
LIDOCAINE HYDROCHLORIDE LIDOCAINE 40 mg

Inactive Ingredients

Ingredient Name Strength
water
DIMETHYL SULFONE
GLYCYRRHIZA GLABRA
POTASSIUM SORBATE
PEPPERMINT OIL
propylene glycol
TEA TREE OIL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE, SPRAY
2 60 in 1 BOTTLE, SPRAY
3 NDC:65121-209-32 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-02-06


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Be sure to consult your doctor before taking any medication!
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