Active Ingredient
Menthol 1.0%
Maximum Strength Medicated Foot Powder
FDA Label NDC 49035-795
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walmart Stores Inc for the product Maximum Strength Medicated Foot Powder (NDC 49035-795). 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, purpose, use, warnings, when using this product, stop and consult a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
External analgesic
Use
for the temporary relief of pain and itching associated with
-minor cuts
-scrapes
-sunburn
-insect bites
-prickly heat
-rashes
-minor burns
-minor skin irritation
-dries the oozing of poison ivy, oak and sumac.
Warnings
For external use only.
When Using This Product
- avoid contact with eyes. Not for genital area
Stop And Consult A Doctor If
- conditions worsens
- redness, irritation, swelling or pain persist or increases
- symptoms do not get better within 7 days or clear up and occur again within a few days
Keep Out Of Reach Of Children.
In case of accidental ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
- adults and children 2 years of age and over: apply freely up to 3 or 4 times daily
- children under 2 years: consult a physician
- For best results, dry skin thoroughly before use.
Inactive Ingredients
benzethonium chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, Zea mays (corn) starch
* Please review the disclaimer below.
