FDA Label for Eez-away Relief
View Indications, Usage & Precautions
Eez-away Relief Product Label
The following document was submitted to the FDA by the labeler of this product Eezaway Relief Inc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient:
Menthol 1.25%
Otc - Purpose
Liquid Analgesic
Otc - 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.
Otc - Questions
To reorder call: 302-339-3030
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