EEZ-AWAY PAIN RELIEF- menthol liquid

eez-away Pain Relief by

Drug Labeling and Warnings

eez-away Pain Relief by is a Otc medication manufactured, distributed, or labeled by EEZAWAY RELIEF INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

QUESTIONS

To reorder call:

1-877 600 0016

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

EEZ-AWAY PAIN RELIEF 
menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69678-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	2.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
PEG-75 LANOLIN (UNII: 09179OX7TB)
POLYOXYL-10 OLEYL ETHER (UNII: JD797EF70J)
PPG-20 METHYL GLUCOSE ETHER (UNII: 3WV1T97D3K)
IODINE (UNII: 9679TC07X4)
SODIUM IODIDE (UNII: F5WR8N145C)
ALCOHOL (UNII: 3K9958V90M)
SODIUM THIOSULFATE (UNII: HX1032V43M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69678-111-02	84 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/24/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/24/2018

Labeler - EEZAWAY RELIEF INC (079751465)