TINACTIN DEODORANT- tolnaftate aerosol, powder 
Bayer HealthCare LLC.

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Tinactin Deodorant Powder Spray Talc Free

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, hydroxypropyl cellulose, isobutane, kaolin, magnesium stearate, PPG-12-Buteth-16, SD Alcohol 40-B (9% v/v),zea mays (corn) starch

Questions?

1-866-360-3266 or visit us at www.tinactin.com

PRINCIPAL DISPLAY PANEL - 133 g Can Label

TOUGH ACTIN' ®



Tinactin
®

tolnaftate ANTIFUNGAL


CURES AND PREVENTS

MOST ATHLETE'S FOOT

Relieves:

DEODORANT
POWDER SPRAY

Fights Odor

Talc Free

NET WT 133g (4.6 oz) PDP

TINACTIN  DEODORANT
tolnaftate aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0137
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
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
KAOLIN (UNII: 24H4NWX5CO)  
STARCH, CORN (UNII: O8232NY3SJ)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ISOBUTANE (UNII: BXR49TP611)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
Colorwhite (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0137-1133 g in 1 CAN; Type 0: Not a Combination Product03/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00503/01/2024
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 4/2024
Document Id: 1751d576-e94b-d7d1-e063-6294a90a03ff
Set id: 1751d576-e94a-d7d1-e063-6294a90a03ff
Version: 1
Effective Time: 20240430
 
Bayer HealthCare LLC.