TopCare Medicated Foot Powder

TopCare Medicated Foot Powder

Drug Labeling and Warnings

Drug Details

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MENTHOL- maximum strength medicated foot powder powder 
Topco Associates LLC

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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TopCare Medicated Foot Powder

​Active ingredient

Menthol 1.0%

Purpose

External analgesic

​Use

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

TOPCARE

Medicated

Foot Powder

TRIPLE RELIEF FORMULA

Menthol 1.0%

  • External analgesic
  • Relieves itching
  • Absorbs moisture
  • Controls foot odor

NET WT 10 OZ (283 g)

Top Care_Medicated Foot Powder_51-113TC.jpg

MENTHOL 
maximum strength medicated foot powder powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 36800-263
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
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
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 36800-263-10283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/18/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/18/2014
Labeler - Topco Associates LLC (006935977)

Revised: 11/2019
 
Topco Associates LLC


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