Skip to Content

← See all Maximum Strength Medicated Foot Powder brands

Maximum Strength Medicated Foot Powder

Medically reviewed on October 26, 2016

Dosage form: powder
Ingredients: MENTHOL 0.1g in 1g
Labeler: Target Corporation
NDC Code: 11673-510

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 1-800-910-6874

Principal Display Panel

Maximum strength
Medicated Foot Powder


Menthol 1%
External analgesic

Compared to Gold Bond® Medicated Foot Powder*

triple relief formula helps absorb moisture
helps relieve itching and control foot odor

NET WT 10 OZ (283g)

MAXIMUM STRENGTH MEDICATED FOOT POWDER 
medicated foot powder powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-510
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL0.1 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZETHONIUM CHLORIDE 
EUCALYPTUS OIL 
ACACIA 
PEPPERMINT OIL 
SODIUM BICARBONATE 
TALC 
Packaging
#Item CodePackage Description
1NDC:11673-510-10283 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/30/2013
Labeler - Target Corporation (006961700)

 
Target Corporation

← See all Maximum Strength Medicated Foot Powder brands

Further information

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

Hide