Skip to Content

Blistex Odor Eaters Medicated Foot

Medically reviewed on Jan 23, 2018

Dosage form: powder
Ingredients: MENTHOL, UNSPECIFIED FORM 1g in 100g
Labeler: Blistex Inc.
NDC Code: 10157-3101

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.

Blistex Odor Eaters® Medicated Foot Powder

Drug Facts

Active ingredient

Menthol 1.0% (w/w)

Purpose

External Analgesic

Uses
  • For the temporary relief of pain and itching associated with minor skin irritations

Warnings

For external use only

When using this product avoid contact with eyes

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.

Keep out of reach of children. If swallowed, 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 physician.
  • Thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. For best results apply to affected areas up to 3 or 4 times daily. Sprinkle inside shoes and/or socks for maximum freshness.

Inactive ingredients

avena sativa kernel flour (collodial oatmeal), benzethonium chloride, eucalyptus globulus leaf oil, gum arabic, sodium bicarbonate, sodium polyacrylate (crosslinked), tricalcium phosphate, zea mays (corn) starch

PRINCIPAL DISPLAY PANEL - 142 g Bottle Label

NEW!

NDC 10157-3101-1

Odor-
Eaters®

3
ADVANCED
ODOR/WETNESS
FIGHTERS

MEDICATED
FOOT POWDER

MENTHOL 1% W/W EXTERNAL ANALGESIC

Controls Odor & Wetness
+ Relieves Itching & Irritation

ALL-DAY
EFFECTIVENESS

STOPS
ODOR

GUARANTEED!

Net Wt.
5 oz. (142 g)

BLISTEX ODOR EATERS MEDICATED FOOT 
menthol, unspecified form powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10157-3101
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (MENTHOL, UNSPECIFIED FORM) MENTHOL, UNSPECIFIED FORM1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
OATMEAL 
BENZETHONIUM CHLORIDE 
EUCALYPTUS OIL 
ACACIA 
SODIUM BICARBONATE 
SODIUM POLYACRYLATE (8000 MW) 
TRICALCIUM PHOSPHATE 
STARCH, CORN 
Packaging
#Item CodePackage Description
1NDC:10157-3101-1142 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34802/01/2015
Labeler - Blistex Inc. (005126354)
Establishment
NameAddressID/FEIOperations
Blistex Inc.005126354MANUFACTURE(10157-3101)

 
Blistex Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide