Active Ingredient
Menthol 1.0%
Menthol Powder
FDA Label NDC 36800-252
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates Llc for the product Menthol (NDC 36800-252). 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 skin irritation
Warnings
For external use only.
When Using This Product
- avoid contact with eyes
Stop And Consult A Doctor If
- conditions worsens
- symptoms persists for more than 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 right away.
Directions
- adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times daily
- children under 2 years of age, consult a doctor
- wash and dry feet thoroughly
- sprinkle powder liberally on feet, between toes and on bottoms of feet
Inactive Ingredients
benzathonium Chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, zea mays (corn) starch
Questions?
Call - 1-888-423-0139
Principal Display Panel
Top Care health
MAXIMUM STRENGTH
Medicated Foot Powder
MENTHOL 1%
EXTERNAL ANALGESIC
TALC- FREE
Triple-Action Formula
- Absorbs Moisture
- Relieves Itching
- Helps Control Foot Odor
NET WT 10 OZ (283g)
* Please review the disclaimer below.
