MAXIMUM STRENGTH MEDICATED FOOT POWDER- medicated foot powder powder 
Walmart Stores 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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Equate Medicated Foot Powder Menthol 1%

​Active ingredient

Menthol 1.0%

​Purpose

External analgesic

​Use

for the temporary relief of pain and itching associated with

-minor cuts

-scrapes

-sunburn

-insect bites

-prickly heat

-rashes

-minor burns

-minor skin irritation

-dries the oozing of poison ivy, oak and sumac.

​Warnings

​For external use only.

​When using this product

  • avoid contact with eyes. Not for genital area

Stop and consult a doctor if

  • conditions worsens
  • redness, irritation, swelling or pain persist or increases
  • symptoms do not get better within 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 (1-800-222-1222) right away.

​Directions

​Inactive ingredients

benzethonium chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, Zea mays (corn) starch

Maximum Strength Medicated Foot Powder

label

MAXIMUM STRENGTH MEDICATED FOOT POWDER 
medicated foot powder powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-795
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.1 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
ZEA MAYS WHOLE (UNII: 1G5HNE09V8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-795-01283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/01/2020
Labeler - Walmart Stores Inc (051957769)

Revised: 9/2020
Document Id: b0794d48-eb8c-55c9-e053-2995a90a5b38
Set id: b0794d48-eb8b-55c9-e053-2995a90a5b38
Version: 1
Effective Time: 20200929
 
Walmart Stores Inc