Active Ingredient
Menthol 1.0%
Walgreens Medicated Foot Powder
FDA Label NDC 42669-100
Full FDA labeling including 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, warning, 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
Purpose
External Analgesic
Uses
For the temporary relief of pain and itch associate with minor skin irritations on the foot
Warning
- 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
Thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottom of feet and in shoes
Inactive Ingredients
Talc, Sodium Bicarbonate, Acacia, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil
Principal Display Panel
NDC 42669-100-10
WALGREENS FOOT POWDER
Compare to Gold Bond Medicated Foot Powder active ingredient
Foot Powder
MENTHOL 1.0%/ EXTERNAL ANALGESIC
MAXIMUM STRENGTH
MEDICATED
Absorbs Moisture
Helps control foot odor
NET WT 10 OZ (283 g)
Label (10)
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