LOTRIMIN DAILY PREVENTION- tolnaftate 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 Powder UI 1612510

Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Use

Use

• clinically proven to prevent most athlete' s foot with daily use

Warnings

For external use only

Do not use on children under 2 years of age unless directed by a doctor

When using this product avoid contact with the eyes

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

• to prevent athlete's foot, wash the feet and dry thoroughly.

• apply 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 socks at least

once daily.

Other information

Other information

store between 20º to 25ºC (68º– 77ºF)

Inactive ingredients

benzethonium chloride;corn starch, kaolin;sodium bicarbonate

Questions

Questions? 1-866-360-3266

Package Display 3 oz. label

LOTRIMIN® AF

TOLNAFTATE ANTIFUNGAL

medicated foot powder

DAILY

PREVENTION

clinically proven to

prevent most

athlete's foot

NET WT 90g (3 OZ)

Lotrimin Daily Prev Powder 0011 Front

Lotrimin Daily Prev Powder 0011 Back

LOTRIMIN DAILY PREVENTION 
tolnaftate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0011
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
KAOLIN (UNII: 24H4NWX5CO)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
STARCH, CORN (UNII: O8232NY3SJ)  
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0011-190 g in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
2NDC:11523-0011-228 g in 1 BOTTLE; Type 0: Not a Combination Product11/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C02/14/2020
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 9/2023
Document Id: 05548b3f-79e2-24c2-e063-6394a90ad2d7
Set id: 9e8f9211-e85d-725a-e053-2995a90a09b3
Version: 5
Effective Time: 20230914
 
Bayer HealthCare LLC.