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 Davion, 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 1.0%
Purpose
External Analgesic
Uses
Temporary relief of pain and itch associated with:
- minor cuts
- sunburn
- insect bites
- scrapes
- minor burns
- minor skin irritations
Warning
- For external use only
- Avoid contact with eyes
Stop Use And Ask A Doctor If
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again within few days
Keep Out Of Reach Of Children
In case of accidental ingestion, get medical help or contact a poison control center right away.
Directions
Remove seal beneath cap before first use. Do not use if seal is broken
- adults and children 2 years and older - apply freely upto 3 or 4 times daily
- children under 2 years - ask a doctor
For best results, dry skin throughly before applying
Inactive Ingredients
Zea Mays (Corn) Starch, Tricalcium Phosphate, Sodium Bicarbonate, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil
Principal Display Panel
NDC 42669-283-01
CVS HEALTH Compared to the active ingredient in Maximum Strength Gold bond Medicated Foot Powder*
MAXIMUM STRENGTH Medicated Foot Powder WITH CORNSTARCG
- Triple Relief: controls odor, absorbs moisture & relieves itc
- Soothing formula
- Clinically tested
- Talc free
NET WT 10 OZ (283 g)
* Please review the disclaimer below.