Eez-away Pain Relief
FDA Label NDC 69678-111
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Eezaway Relief Inc for the product Eez-away Pain Relief (NDC 69678-111). 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 drug facts, active ingredient:, purpose, uses, warnings:, keep out of reach of children., directions, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
Otc - Questions
To reorder call:
1-877 600 0016
Other
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Distributed exclusively by
eez-Away Inc. P.O. Box 161, Hunterville, NC 28070
Packaging
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