MENTHOL- maximum strength medicated foot powder powder 
Premier Brands of America Inc.

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.

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Maximum Strength Foot Powder

​Active ingredient

Menthol 1.0%

Purpose

External analgesic

Use

for the temporary relief of pain and itching associated with minor skin irritations 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

Maximum strength

Foot Powder

Medicated

Menthol 1% External Analgesic

Triple Relief Formula

  • Absorb moisture
  • Relieve itching
  • Helps control foot odor

NET WT 10 OZ (283g)

medicated foot powder

MENTHOL 
maximum strength medicated foot powder powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-136
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.83 g  in 283 g
Inactive Ingredients
Ingredient NameStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
ACACIA (UNII: 5C5403N26O)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:56104-136-10283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/201307/13/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/201307/13/2021
Labeler - Premier Brands of America Inc. (117557458)

Revised: 7/2021
Document Id: c7049305-c484-3e7c-e053-2995a90a4c96
Set id: b7703c16-a28e-4a09-aa6c-6fbf0879f8af
Version: 5
Effective Time: 20210716
 
Premier Brands of America Inc.