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eez-away Pain Relief

Medically reviewed by Drugs.com. Last updated on Nov 1, 2021.

Dosage form: liquid
Ingredients: MENTHOL, UNSPECIFIED FORM 2.5g in 100mL
Labeler: EEZAWAY RELIEF INC
NDC Code: 69678-111

eez-away Pain Relief

Drug Facts

Active ingredient:

Menthol 2.50%

Purpose

Topical Analgesic

Uses

for temporary relief of minor aches and pains of muscles and joints associated with • bruises • sprains • arthritis • strains

Warnings:

For external use only

When using this product  

Do not bandage tightly • avoid contact with eyes • do not apply to wounds or damaged skin • do not use with heating pads or other heating devices.

Stop use and ask a doctor if

• Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within 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 10 times a day as needed for pain.

• children under 12 years of age: do not use, consult a doctor.

Inactive ingredients:

Isopropyl Alcohol, Deionized Water, PEG-75 Lanolin, Oleth-10, PPG-20 Methyl Glucose Ether, Iodine, Sodium Iodide, Ethyl Alcohol, Sodium Thiosulfate Pentahydrate, Fragrance.

To reorder call:

1-877 600 0016

NEW! EXTRA STRENGTH ROLL-ON

Recommended by

  • Top Physicians
  • Professional Athletes
  • Trainers

Distributed exclusively by

eez-Away Inc. P.O. Box 161, Hunterville, NC 28070

Packaging

EEZ-AWAY PAIN RELIEF 
menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69678-111
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (MENTHOL) MENTHOL, UNSPECIFIED FORM2.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL 
WATER 
PEG-75 LANOLIN 
POLYOXYL-10 OLEYL ETHER 
PPG-20 METHYL GLUCOSE ETHER 
IODINE 
SODIUM IODIDE 
ALCOHOL 
SODIUM THIOSULFATE 
Packaging
#Item CodePackage Description
1NDC:69678-111-0284 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/24/2018
Labeler - EEZAWAY RELIEF INC (079751465)

 
EEZAWAY RELIEF INC

Further information

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