FDA Label for Menthol
View Indications, Usage & Precautions
Menthol Product Label
The following document was submitted to the FDA by the labeler of this product Target Corporation. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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: do not use, consult a doctor
- wash and dry feet thoroughly
- sprinkle powder liberally on feet, between toes and on bottoms of feet
Inactive Ingredients
zea mays (corn) starch, sodium bicarbonate, tricalcium phosphate, benzethonium chloride, eucalyptus globulus leaf oil, mentha piperita (peppermint) oil
Questions?
Call 1-866-964-0939
Recent Major Changes
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Compare to active ingredient in Gold Bond
Medicated Foot Powder
Maximum Strength
Medicated
Foot Powder
Menthol 1 %- External Analgesic
- Triple- action formula absorbs
- Talc free
moisture, relieves itching and
helps control foot odor
up&up
NET WT. 10 OZ. (283 g)
* Please review the disclaimer below.
