EEZ-AWAY RELIEF- menthol spray 
EEZAWAY RELIEF INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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eez-away RELIEF

ACTIVE INGREDIENT:

Menthol 1.25%

Liquid Analgesic

Keep out of reach of children.

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

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

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.

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.

To reorder call: 302-339-3030

Packaging

eez-label

EEZ-AWAY RELIEF 
menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69678-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.25 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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
Colorbrown (amber) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69678-101-08236.6 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/19/2015
2NDC:69678-101-06177.4 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/31/2017
3NDC:69678-101-04118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/31/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/19/2015
Labeler - EEZAWAY RELIEF INC (079751465)
Establishment
NameAddressID/FEIBusiness Operations
Topiderm Inc.049121643manufacture(69678-101)

Revised: 6/2017
Document Id: c3b7cf84-100a-4902-8e2a-faa762aba10f
Set id: 5eb7deb4-e7e4-4ee3-a002-b982b59fb7cf
Version: 3
Effective Time: 20170606
 
EEZAWAY RELIEF INC