Active Ingredient:
Menthol 1.25%
Eez-away Relief
FDA Label NDC 69678-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Eezaway Relief Inc for the product Eez-away Relief (NDC 69678-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient:, otc - purpose, otc - keep out of reach of children, indications & usage, precautions, warnings, directions for use, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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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