FDA Label for Maximum Strength Medicated Foot Powder
View Indications, Usage & Precautions
Maximum Strength Medicated Foot Powder Product Label
The following document was submitted to the FDA by the labeler of this product Jell Pharmaceuticals Pvt. Ltd.. 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 1.0%
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
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