TINACTIN- tolnaftate aerosol, powder 
Bayer HealthCare LLC.

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Tinactin ® AF Powder Spray Talc Free

Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

Warnings

For external use only

Flammable: Do not use near heat, flame, 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
  • use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
  • contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F.

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

Other information

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

Inactive ingredients

butylated hydroxytoluene, hydroxypropyl cellulose, isobutane,kaolin, magnesium stearate, PPG-12-buteth-16, SD alcohol 40-B (9% w/w), zea mays (corn) starch

Questions?

1-866-360-3266

TOUGH ACTIN' ®

Tinactin ®

tolnaftate ANTIFUNGAL

Cures and prevents

most athlete's foot

Relieves

POWDER SPRAY

goes on dry

talc free

NET WT 133g (4.6 oz)

TINACTIN AF Powder Spray 133g Talc Free

TINACTIN 
tolnaftate aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0139
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
STARCH, CORN (UNII: O8232NY3SJ)  
ISOBUTANE (UNII: BXR49TP611)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
KAOLIN (UNII: 24H4NWX5CO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
Product Characteristics
Colorwhite (White to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0139-1133 g in 1 CAN; Type 0: Not a Combination Product11/29/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00511/29/2023
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 5/2024
Document Id: 18e509e4-bb1d-7333-e063-6394a90aa5ab
Set id: 0beda157-efd2-5245-e063-6394a90a6911
Version: 2
Effective Time: 20240520
 
Bayer HealthCare LLC.