Menthol Powder
FDA Label NDC 63941-558

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Valu Merchandisers, Co for the product Menthol (NDC 63941-558). 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 use and ask 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

​Active Ingredient

Menthol 1.0%

Purpose

External analgesic

​Use

for the temporary relief of pain and itching associated with minor skin irritations

​Warnings

​For external use only.

When Using This Product

  • avoid contact with the eyes

Stop Use And Ask 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.

If swallowed, 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

benzethonium chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, zea mays (corn) starch

​Questions?

Call 1-866-964-0939

Principal Display Panel

Best Choice

MAXIMUM STRENGTH

Medicated Foot Powder

MENTHOL 1.0% / EXTERNAL ANALGESIC

TALC-FREE

  • Absorbs Moisture
  • Relieves Itching
  • Helps Control Foot Odor

    • NET WT 10 oz (283g)

* Please review the disclaimer below.