LOTRIMIN DAILY PREVENTION DEO- 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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Lotrimin Daily Prevention Deo Powder Spray UI 1612507

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

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.

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.
do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120ºF

Directions

Directions

to prevent athlete’s foot, wash the feet and dry thoroughly.
shake can well and spray a thin layer of the product on the feet once or twice daily (morning and/or night)
supervise children in the use of this product.
pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

Other information

Other Information

store between 20º to 25ºC (68º– 77ºF)

Inactive Ingredients

butylated hydroxytoluene, fragrance, isobutane, PEG-12-Buteth-16, SD alcohol 40B (10.5% v/v), talc

Questions? 1-866-360-3266

Display can 160 grams

Lotrimin®AF

TOLNAFTATE ANTIFUNGAL

deodorant powder spray

DAILY PREVENTION

clinically proven to

prevent most

athlete's foot

NET WT 160 g (5.6 OZ)

Can label

LOTRIMIN DAILY PREVENTION DEO 
tolnaftate aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0010
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
ALCOHOL (UNII: 3K9958V90M)  
TALC (UNII: 7SEV7J4R1U)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
ISOBUTANE (UNII: BXR49TP611)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0010-1160 g in 1 CAN; Type 0: Not a Combination Product02/14/2020
2NDC:11523-0010-2133 g in 1 CAN; Type 0: Not a Combination Product02/14/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C02/14/2020
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 7/2023
Document Id: ffd3dbaf-b9e2-fd72-e053-6394a90a0549
Set id: 9e8bfb78-ad81-93d0-e053-2995a90aa41d
Version: 8
Effective Time: 20230706
 
Bayer HealthCare LLC.