LOTRIMIN DAILY PREVENT DEODORANT- tolnaftate aerosol, powder 
Bayer HealthCare LLC.

----------

Lotrimin Daily Prevention Powder Spray TALC FREE UI 1615422

Drug Facts

Active Ingredient

(To Deliver)Tolnaftate 1%

Purpose

Antifungal

Use

Use

clinically proven to prevent most athlete’s foot with daily use

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 temperatures above 120ºF.

Stop use and ask a doctor if irritation occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions

Other information

Other Information

store between 20º to 25ºC (68º– 77ºF)

Inactive Ingredients

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

Questions?1-866-360-3266 or visit us at www.lotrimin.com

Display can 160 grams

PDP

LOTRIMIN  DAILY PREVENT DEODORANT
tolnaftate aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0136
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
MAGNESIUM STEARATE (UNII: 70097M6I30)  
STARCH, CORN (UNII: O8232NY3SJ)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ALCOHOL (UNII: 3K9958V90M)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
ISOBUTANE (UNII: BXR49TP611)  
KAOLIN (UNII: 24H4NWX5CO)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0136-1160 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: 6/2024
Document Id: 1bb961cd-b6e5-3aff-e063-6394a90a432e
Set id: 1bb961cd-b6e6-3aff-e063-6394a90a432e
Version: 1
Effective Time: 20240625
 
Bayer HealthCare LLC.