LOTRIMIN DAILY SWEAT AND ODOR CONTROL- topical starch 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 Sweat and Odor Control Powder UI 1612345

Drug Facts

Active ingredient

Topical starch 83.7%

Purpose

Skin Protectant

Use

Use

temporarily protects and helps relieve minor skin irritation

Warnings

For external use only

Do not use on broken skin.

When using this product

• Do not get into eyes

• Keep away from face and mouth to avoid breathing it

Stop use and ask a doctor if

  • Condition worsens
  • Symptoms last more than 7 days or clear up and occur again within a few days

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

Directions

Directions

Apply as needed

Inactive ingredients

benzethonium chloride,camphor,eucalyptus globulus leaf oil, fragrance, kaolin,lemon oil, zinc oxide

Questions

Questions? 1-866-360-3266

Package display

LOTRIMIN

TOPICAL STARCH SKIN PROTECTANT

medicated foot powder

DAILY SWEAT

& ODOR CONTROL

6 odor-fighting

ingredients to control odor

NET WT 177 G (6.25 OZ)

Lotrimin Sweat and Odor Powder 0012 Front

Lotrimin Sweat and Odor Powder 0012 Back

LOTRIMIN DAILY SWEAT AND ODOR CONTROL 
topical starch powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STARCH, CORN (UNII: O8232NY3SJ) (STARCH, CORN - UNII:O8232NY3SJ) STARCH, CORN837 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
EUCALYPTUS OIL (UNII: 2R04ONI662)  
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
LEMON OIL (UNII: I9GRO824LL)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
KAOLIN (UNII: 24H4NWX5CO)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0012-1177 g in 1 BOTTLE; Type 0: Not a Combination Product02/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34702/17/2020
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 9/2023
Document Id: 05544b73-ea58-dc99-e063-6394a90a9ea3
Set id: 9ec5c80d-b550-496f-e053-2a95a90a5489
Version: 4
Effective Time: 20230914
 
Bayer HealthCare LLC.