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 Harmon Store Inc.. 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 irritation on the foot
Warnings
For external use only.
When Using This Product
- avoid contact with eyes
Stop And Consult 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.
In case of accidental ingestion, 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, consult a doctor
- wash and dry feet thoroughly
- sprinkle powder liberally on feet, between toes and on bottoms of feet
Inactive Ingredients
benzethonium chloride, eucalytus oil, gum acacia, peppermint oil, sodium bicarbonate, talc
Questions?
Call 1-866-964-0939
Principal Display Panel
CoreValues
Maximum Strength
Medicated Foot Powder
Menthol 1%
Triple-Action
Formula
- Absorbs Moisture
- Relieves Itching
- Controls Foot Odor
Net Wt 10 OZ (283 g)
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