TINACTIN  ANTIFUNGAL- 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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Tinactin ®



Antifungal

Drug Facts

Active ingredients

(To Deliver) 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 the contents can be harmful or fatal.
  • contents under pressure. do not puncture or incinerate. Do not store at temperatures 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

Inactive Ingredients

Butylated Hydroxytoluene, Fragrance, Isobutane, PPG-12-Buteth-16, SD Alcohol 40-B (10.5% v/v),Talc

Questions?

1-866-360-3266

PRINCIPAL DISPLAY PANEL - 133 g Can Label

NDC 11523-4162-1

TOUGH ACTIN' ®

Tinactin
®

ANTIFUNGAL

tolnaftate

Cures and

prevents most

athlete's foot

DEODORANT

POWDER SPRAY

fights odor all day

Relieves itching & burning

NET WT 133g (4.6 oz)

Can image

TINACTIN   ANTIFUNGAL
tolnaftate aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-4162
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
ISOBUTANE (UNII: BXR49TP611)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
TALC (UNII: 7SEV7J4R1U)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
Product Characteristics
Colorwhite (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-4162-1133 g in 1 CAN; Type 0: Not a Combination Product02/28/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C02/28/2014
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 9/2023
Document Id: 0553a56d-475c-e952-e063-6294a90abe3d
Set id: 5f95be36-6efa-4dfb-9a40-88f4ce1de2b3
Version: 8
Effective Time: 20230914
 
Bayer HealthCare LLC.