MAXIMUM STRENGTH MEDICATED FOOT POWDER- menthol powder 
CVS

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MAXIMUM STRENGTH Medicated Foot Powder with Corn Starch

Active Ingredient

Menthol 1.0%

Purpose

External Analgesic

Uses

Temporary relief of pain and itch associate with:

  • minor cuts
  • sunburn
  • insect bites
  • scrapes
  • minor burns
  • minor skin irritations

Warning

  • For external use only
  • Avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within 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

Remove seal beneath cap before first use. Do not use if seal is broken

  • adults and children 2 years and older - apply freely upto 3 or 4 times daily
  • children under 2 years - ask a doctor

For best results, dry skin throughly before applying

Inactive ingredients

Zea Mays (Corn) Starch, Tricalcium Phosphate,  Sodium Bicarbonate, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil

PRINCIPAL DISPLAY PANEL

NDC 69842-283-01

CVS HEALTH Compared to the active ingredient in Maximum Strength Gold bond Medicated Foot Powder*

MAXIMUM STRENGTH Medicated Foot Powder WITH CORNSTARCG

  • Triple Relief: controls odor, absorbs moisture & relieves itc
  • Soothing formula
  • Clinically tested
  • Talc free

NET WT 10 OZ (283 g)

Label

MAXIMUM STRENGTH MEDICATED FOOT POWDER 
menthol powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-283
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-283-01283 g in 1 BOTTLE; Type 0: Not a Combination Product01/30/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/30/201812/13/2023
Labeler - CVS (062312574)
Registrant - Davion, Inc (174542928)
Establishment
NameAddressID/FEIBusiness Operations
Davion, Inc079536689manufacture(69842-283)

Revised: 1/2024
Document Id: 0e24855a-6c52-5087-e063-6394a90ae1c7
Set id: 22e9b151-3020-4202-af27-d73fdaf9377c
Version: 2
Effective Time: 20240104
 
CVS