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Oxy Rub Pain Relief

Dosage form: cream
Ingredients: MENTHOL 12.5mg in 1g
Labeler: Healthy Directions
NDC code: 70015-645

Medically reviewed by Drugs.com. Last updated on Feb 6, 2024.

Oxy Rub Pain Relief

Drug Facts

Active Ingredient

Menthol 1.25%

Purpose

Topical Analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints associated with

  • 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 imitation develops
  • condition worsens or symptoms persist for more thyan 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.

Other information

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

Inactive ingredients

C13-14 Isoparaffin, Citrus Aurantium Dulcis (Orange) Oil, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glyceryl Stearate, Laureth-7, Oxidized Corn Oil, PEG-100 Stearate, Phenoxyethanol, Polycrylamide, Polysorbate-20, Water

Product Label

OXY RUB PAIN RELIEF 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70015-645
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL12.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
C13-14 ISOPARAFFIN 
ETHYLHEXYLGLYCERIN 
EUCALYPTUS OIL 
GLYCERYL MONOSTEARATE 
LAURETH-7 
PEG-100 STEARATE 
PHENOXYETHANOL 
POLYSORBATE 20 
WATER 
Packaging
#Item CodePackage Description
1NDC:70015-645-0257 g in 1 TUBE
2NDC:70015-645-04114 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/01/2013
Labeler - Healthy Directions (150261183)

Document Id: 48a91b6c-d99e-4a92-e054-00144ff8d46c
Set id: c2803a42-3a23-44d6-9c56-27a12959ba45
Version: 3
Effective Time: 20170216
 
Healthy Directions

Further information

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

Medical Disclaimer