MENTHOL- maximum strength medicated foot powder talc free powder 
Target Corporation

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Medicated Foot Powder -Talc Free

Active ingredient

Menthol 1.0%

Purpose

External analgesic

Use

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

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

Inactive ingredients

benzathonium Chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, zea mays (corn) starch

Questions?

Call 1-800-910-6874

Principal Display Panel

maximum strength

medicated

foot powder

menthol 1 %

external analgesic

talc- free

triple action formula absorbs moisture,

relieve itching and helps control foot odor

NET WT 10 OZ (283 g)

medicated powder

MENTHOL 
maximum strength medicated foot powder talc free powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-511
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.8 g  in 283 g
Inactive Ingredients
Ingredient NameStrength
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-511-10283 g in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package11/27/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/27/2017
Labeler - Target Corporation (006961700)

Revised: 2/2024
Document Id: 1149d86e-6efe-dcda-e063-6294a90a1dde
Set id: cee20e8e-3a44-437b-83ef-0f5303fece2a
Version: 5
Effective Time: 20240213
 
Target Corporation