Walgreens Medicated Foot Powder
FDA Label NDC 42669-100

9 label sections · Submitted to the FDA by Davion, Inc · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Davion, Inc for the product Walgreens Medicated Foot Powder (NDC 42669-100). 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, uses, 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

Uses

temporary relief of the pain and itch associated with:

  • minor cuts
  • sunburn
  • insect bites
  • scrapes
  • minor burns
  • minor skin irritations

Warnings

For external use only

When Using This Product

  • Avoid contact with eyes

Stop Use And Ask A Doctor If

  • condition 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 and older - apply freely upto 3 or 4 times daily
  • children under 2 years - ask a doctor before using
    For best results, dry skin thoroughly before applying.

Inactive Ingredients

Zea Mays (Corn) Starch, Tricalcium Phosphate, Sodium Bicarbonate, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil

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