Active Ingredient
Menthol 1.0%
H-e-b Medicated Corn Starch Foot Powder
FDA Label NDC 42669-218
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 H-e-b Medicated Corn Starch Foot Powder (NDC 42669-218). 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, stop use and ask a doctor if, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
External Analgesic
Uses
Temporary relief of pain and itch associate with:
- Minor Cuts
- Sunburn
- Insect Bites
- Scrapes
- Minor Burns
- Minor Skin Irritations
Warnings
- 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
- 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 42669-218-10
Compare to Gold Bond ® Medicated Foot Powder active ingredient*
H-E-B Medicated Corn Starch Foot Powder
TRIPLE RELIEF FORMULA
- Controls Odor
- Absorbs Moisture
- Relieves Itching
Talc-Free
NET WT. 10 OZ (283g)
Label (218)
* Please review the disclaimer below.
