OxyRub Pain Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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OxyRub Pain Relief

Pure Source Inc.
Pure Source Inc.

OxyRub Pain Relief Cream


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OxyRub Pain Relief Cream

Active Ingredient

Menthol (1.25%)

Purpose

Topical Analgesic

OxyRub Pain Relief Uses

temporarily relieves minor aches and pains of muscles and joints associated

  • simple backaches
  • arthritis
  • strains
  • sprains 
  • bruises

Warnings

For external use only.

  • Use only as directed.

Do not use

  • with a heating pad, may blister skin
  • on open wounds or damaged skin

Ask a doctor before use if you have redness over the affected area

When using this product

  • Avoid contact with eyes
  • Do not bandage tightly

Stop use and consult a doctor if

  • skin redness or excessive skin irritation develops
  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again in a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 12 years of age and older. Apply to affected area no more than 3-4 times daily.
Children under 12 years of age, consult a doctor.

OxyRub Pain Relief Other information

Store at room temperature. For Lot Number and Expiration Date, see crimp at end of tube.

Inactive Ingredients

Bitter Orange Oil, C13-14 Isoparaffin, Caprylhydroxomic Acid, Caprylyl Glycol, Eucalyptus Oil, Glycerin, Laureth-7, Oxidized Corn Oil, Polyacrylamide (1000 MW), Polysorbate 20, Water

OxyRub Pain Relief Cream 4oz/114g (65121-113-04)

OxyRub Pain Relief

OxyRub Pain Relief

MENTHOL CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65121-113
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 1.25 g

Inactive Ingredients

Ingredient Name Strength
Bitter Orange Oil
C13-14 ISOPARAFFIN
CAPRYLHYDROXAMIC ACID
CAPRYLYL GLYCOL
EUCALYPTUS OIL
GLYCERIN
LAURETH-7
CORN OIL
POLYSORBATE 20
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65121-113-04 114 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-05-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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