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Menthol by Topco Associates LLC

Medically reviewed on December 5, 2017

Dosage form: powder
Ingredients: MENTHOL 2.8g in 283g
Labeler: Topco Associates LLC
NDC Code: 36800-263

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Medicated Foot Powder

​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

TOPCARE

Medicated

Foot Powder

TRIPLE RELIEF FORMULA

Menthol 1%

  • External Analgesic
  • Relieves itching
  • Absorbs moisture
  • Controls foot odor 

Net Wt 10 OZ (283 g)

MENTHOL 
maximum strength medicated foot powder powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-263
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL2.8 g  in 283 g
Inactive Ingredients
Ingredient NameStrength
BENZETHONIUM CHLORIDE 
EUCALYPTUS OIL 
ACACIA 
PEPPERMINT OIL 
SODIUM BICARBONATE 
TALC 
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:36800-263-10283 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/18/2014
Labeler - Topco Associates LLC (006935977)

 
Topco Associates LLC

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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