Active Ingredient
Menthol 1.0%
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Menthol (NDC 82442-211). 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.
Menthol 1.0%
External analgesic
for the temporary relief of pain and itching associated with minor skin irritations
For external use only.
If swallowed, get medical help or contact a Poison Control Center right away.
zea mays (corn) starch, sodium bicarbonate, tricalcium phosphate, benzethonium chloride, eucalyptus globulus leaf oil, mentha piperita (peppermint) oil
Call 1-866-964-0939
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Compare to active ingredient in Gold Bond
Medicated Foot Powder
Maximum Strength
Medicated
Foot Powder
Menthol 1 %- External Analgesic
moisture, relieves itching and
helps control foot odor
up&up
NET WT. 10 OZ. (283 g)
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