EEZ-AWAY RELIEF- menthol spray

eez-away RELIEF by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT:

Menthol 1.25%

PURPOSE

Liquid Analgesic

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INDICATIONS & USAGE

FOR THE TEMPORARY RELIEF OF MINOR ACHES & PAINS ASSOCIATED WITH ARTHRITIS, SIMPLE BACKACHE & SORE, TIRED MUSCLES.

PRECAUTIONS

CAUTION: Do not apply to wounds or damaged skin. If rash or irritation occurs, discontinue use.

WARNINGS

The application of external heat, such as an electric heating pad, may result in excessive skin irritation or burn. Avoid contact with the eyes and mucous membranes. Do not bandage tightly. Do not inhale.

DIRECTIONS FOR USE

Apply EEZ-AWAY® generously to the affected area. Let dry, then re-apply. For maximum pain relief, apply, let dry and re-apply five times daily or as needed.

INACTIVE INGREDIENT

INGREDIENTS: Isopropyl Alcohol, Deionized Water (Aqua), PEG-75 Lanolin, Iodine, Oleth-10, PPG-20 Methyl Glucose Ether Distearate, Sodium Iodide, Sodium Thiosulfate, Ethyl Alcohol, Fragrance.

QUESTIONS

To reorder call: 302-339-3030

Packaging

INGREDIENTS AND APPEARANCE

EEZ-AWAY RELIEF 
menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69678-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
IODINE (UNII: 9679TC07X4)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
POLYOXYL-10 OLEYL ETHER (UNII: JD797EF70J)
PEG-75 LANOLIN (UNII: 09179OX7TB)
PPG-20 METHYL GLUCOSE ETHER DISTEARATE (UNII: 0057334FAB)
SODIUM IODIDE (UNII: F5WR8N145C)
SODIUM THIOSULFATE (UNII: HX1032V43M)

Product Characteristics
Color	brown (amber)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69678-101-08	236.6 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/19/2015
2	NDC: 69678-101-06	177.4 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/31/2017
3	NDC: 69678-101-04	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/31/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/19/2015

Labeler - EEZAWAY RELIEF INC (079751465)

Establishment
Name	Address	ID/FEI	Business Operations
Topiderm Inc.		049121643	manufacture(69678-101)