TOLNAFTATE- foot odor control powder spray aerosol, spray 
Chain Drug Consortium, LLC

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Foot Odor Control Powder Spray

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

Warnings

For external use only.

Flammable:

Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

When using this product

  • do not get into eyes or mouth, if products get into eyes, rinse eyes thoroughly with water.
  • use only as directed

Stop use and ask a doctor if

  • irritation occurs
  • no improvement within 4 weeks

​Do not use

on children under 2 years of age unless directed by a doctor

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

store between 20º and 30ºC (68ºF and 86º)

Inactive ingredients

disteardimonium hectorite, fragrance, isobutane, isopropyl myristate, SD alcohol 40-B, sodium bicarbonate

Questions?

call 1-866-964-0939

Principal Display Panel

Premier Value

Antifungal

Foot Odor

Control

Powder Spray

Tolnaftate 1%

Cures most athlete's foor

and prevents recurrence

Reduces foot odor

Relieves itching,

burning and cracking

NET WT 4.0 OZ (113g)

foot odor control powder spray

TOLNAFTATE 
foot odor control powder spray aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-586
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1.3 g  in 113 g
Inactive Ingredients
Ingredient NameStrength
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
ISOBUTANE (UNII: BXR49TP611)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ALCOHOL (UNII: 3K9958V90M)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-586-03113 g in 1 CAN; Type 0: Not a Combination Product06/01/2006
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00506/01/2006
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 2/2024
Document Id: 1057cd81-618b-f88d-e063-6294a90a1e24
Set id: 059f540a-3233-435e-b54c-98b2302306e2
Version: 7
Effective Time: 20240201
 
Chain Drug Consortium, LLC