Lotrimin Daily Sweat and Odor Control

Manufacturer
Bayer HealthCare LLC.
Effective date
2026-01-16
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:33:32

Label at a glance#

ProductLotrimin Daily Sweat and Odor Control
Active ingredientSTARCH, CORN
Label structure9 sections

Dosage and administration

Directions Apply as needed

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Topical starch 83.7%

OTC - PURPOSE SECTION

Purpose

Skin Protectant

Use

INDICATIONS & USAGE SECTION

Use

temporarily protects and helps relieve minor skin irritation

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - WHEN USING SECTION

When using this product

• Do not get into eyes

• Keep away from face and mouth to avoid breathing it

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Apply as needed

INACTIVE INGREDIENT SECTION

Inactive ingredients

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

Questions

OTC - QUESTIONS SECTION

Questions? 1-866-360-3266

Package display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOTRIMIN

TOPICAL STARCH SKIN PROTECTANT

medicated foot powder

DAILY SWEAT

& ODOR CONTROL

6 odor-fighting

ingredients to control odor

  • super sweat absorbent powder
  • relieves irritation
  • talc-free

NET WT 177 G (6.25 OZ)

Lotrimin Sweat and Odor Powder 0012 FrontLotrimin Sweat and Odor Powder 0012 Front

Lotrimin Sweat and Odor Powder 0012 BackLotrimin Sweat and Odor Powder 0012 Back

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1294098cornstarch 83.7 % Topical PowderPSN6
1294098corn starch 0.837 MG/MG Topical PowderSCD6
1294098cornstarch 83.7 % Topical PowderSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130041100587305GTIN-13: 0041100587305
EAN-13: 0041100587305
GTIN-12: 041100587305
UPC-A: 041100587305
GTIN storage (14 digits): 00041100587305
Lotrimin Sweat and Odor Powder_0012-2.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11523-0012-1Lotrimin Daily Sweat and Odor Control177 g in 1 BOTTLEPOWDER1776

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11523-001211523-0012-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lotrimin Daily Sweat and Odor ControlTOPICAL STARCHBayer HealthCare LLC.9ec5c80d-b550-496f-e053-2a95a90a54892026-01-16WarningsExact identifier
ndc (package): 11523-0012-1
ndc (product): 11523-0012
ndc11 (package): 11523001201
spl id: 488511a8-cba1-6c74-e063-6294a90af1a3
spl set id: 9ec5c80d-b550-496f-e053-2a95a90a5489

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.