TOLNAFTATE- tolnaftate athletes foot powder spray spray 
Walgreens Company

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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Walgreens Athlete’s Foot Powder Spray (Tolnaftate)

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

Warnings

For external use only

Flammable: Do not use near flame or spark or while smoking.

Do not use

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

When using this product

  • avoid contact with the eyes
  • contents under pressure. Do not puncture or incinerate or store at temperatures above 120°F (49°C).
  • use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Stop use and ask a doctor if

  • irritation occurs
  • there is no improvement within 4 weeks

Keep out of reach of children.

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

Directions

Inactive ingredients

alcohol SD 40-B, aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propane, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

Questions or comments?

1-800-719-9260

Principal Display Panel

Athlete’s Foot

Antifungal

Powder Spray

Tolnaftate 1%

Cures & prevents most athlete’s foot

Relieves itching & burning

NET WT 4.6 OZ (130g)

Artwork

TOLNAFTATE 
tolnaftate athletes foot powder spray spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-1746
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1.3 g  in 130 g
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ISOBUTANE (UNII: BXR49TP611)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
ALCOHOL (UNII: 3K9958V90M)  
TALC (UNII: 7SEV7J4R1U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-1746-00130 g in 1 CAN; Type 0: Not a Combination Product10/20/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C10/20/2021
Labeler - Walgreens Company (008965063)

Revised: 1/2023
Document Id: f37ff7a8-eb41-eddd-e053-2995a90a691a
Set id: cecae979-01a5-3415-e053-2995a90a092f
Version: 2
Effective Time: 20230130
 
Walgreens Company