DR. SCHOLLS ODOR-X FOOT AND SNEAKER- tolnaftate aerosol, powder 
Bayer HealthCare 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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Dr. Scholl's ®



Odor-X ® Foot & Sneaker

Drug Facts

Active ingredient

(To Deliver) Tolnaftate 1%

Purpose

Antifungal

Use

helps prevent most athlete's foot with daily use

Warnings

For external use only

Flammable

Do not use while smoking or near heat or flame

When using this product

  • avoid contact with the eyes
  • use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
  • do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

Stop use and ask a doctor if irritation occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For prevention of most athlete's foot:

  • wash and dry feet thoroughly
  • shake can well and spray a thin layer on the feet once or twice daily (morning and/or night)
  • supervise children in the use of this product
  • pay special attention to spaces between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily
  • in case of clogging, clean nozzle with a pin.

Other information

store between 20° to 25°C (68° to 77°F)

Inactive ingredients

butylated hydroxytoluene, fragrance, isobutane, PPG-12-buteth-16, SD alcohol 40-B (10.5% v/v), talc

Questions?

1-866-360-3266

Distributed by

Bayer HealthCare LLC

Whippany, NJ 07981

PRINCIPAL DISPLAY PANEL - 133 g Can Label

NDC 11523-4336-1

Dr. Scholl's®

Odor-X®

FOOT & SNEAKER

SPRAY POWDER

Tolnaftate Antifungal

withTOUGH ACTIN' ®

Tinactin ®

ANTIFUNGAL

Destroys Odor

Instantly

Prevents Most

Athlete's Foot

NET WT. 133g (4.6 OZ)

Label 133 g

DR. SCHOLLS  ODOR-X FOOT AND SNEAKER
tolnaftate aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-4336
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ISOBUTANE (UNII: BXR49TP611)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
Colorwhite (White to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-4336-1133 g in 1 CAN; Type 0: Not a Combination Product09/23/199308/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C09/23/199308/31/2021
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 12/2019
Document Id: 98e730db-4423-6389-e053-2a95a90a49a1
Set id: 868ec234-4553-4c09-ac71-6de22037da1d
Version: 5
Effective Time: 20191204
 
Bayer HealthCare LLC.