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Menthol by Target Corporation

Medically reviewed on Nov 27, 2017

Dosage form: powder
Ingredients: MENTHOL 2.8g in 283g
Labeler: Target Corporation
NDC Code: 11673-511

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 -Talc Free

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

zea mays (corn) starch, tricalcium phosphate, Sodium bicarbonate, benzathonium chloride, eucalyptus oil, peppermint oil. 

Questions?

Call 1-866-964-0939

Principal Display Panel

maximum strength

medicated foot powder

menthol 1 %

external analgesic

talc- free

triple- action formula helps absorb moisture

helps relieve itching and control foot odor

NET WT 10OZ (283g)

MENTHOL 
maximum strength medicated foot powder talc free powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-511
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL2.8 g  in 283 g
Inactive Ingredients
Ingredient NameStrength
ZEA MAYS SUBSP. MAYS WHOLE 
TRICALCIUM PHOSPHATE 
SODIUM BICARBONATE 
BENZETHONIUM CHLORIDE 
EUCALYPTUS OIL 
PEPPERMINT OIL 
Packaging
#Item CodePackage Description
1NDC:11673-511-10283 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/27/2017
Labeler - Target Corporation (006961700)

 
Target Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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