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Menthol by Premier Brands of America Inc.

Medically reviewed on November 1, 2017

Dosage form: powder
Ingredients: MENTHOL 2.83g in 283g
Labeler: Premier Brands of America Inc.
NDC Code: 56104-136

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.

Maximum Strength Foot Powder

​Active ingredient

Menthol 1.0%


External analgesic


for the temporary relief of pain and itching associated with minor skin irritation on the foot


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.

  • 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


call 1-866-964-0939

​Principal Display Panel

Maximum strength

Foot Powder


Menthol 1% External Analgesic

Triple Relief Formula

  • Absorb moisture
  • Relieve itching
  • Helps control foot odor

NET WT 10 OZ (283g)

maximum strength medicated foot powder powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-136
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Product Characteristics
FlavorMINTImprint Code
#Item CodePackage Description
1NDC:56104-136-10283 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/2013
Labeler - Premier Brands of America Inc. (080051232)

Premier Brands of America Inc.

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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.