Lotrimin Daily Prevention Powder Spray TALC FREE UI 1615422

Manufacturer
Bayer HealthCare LLC.
Effective date
2025-12-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:19:41

Label at a glance#

ProductLotrimin Daily Prevent Deodorant
Active ingredientTOLNAFTATE
Label structure10 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

(To Deliver)Tolnaftate 1%

OTC - PURPOSE SECTION

Purpose

Antifungal

Use

INDICATIONS & USAGE SECTION

Use

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

WARNINGS SECTION

Warnings

For external use only

Flammable: Do not use near heat, flame, or while smoking

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation occurs.

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

  • 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 SAFETY INFORMATION

Other Information

store between 20º to 25ºC (68º– 77ºF)

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

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

Display can 160 grams

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
705934tolnaftate 1 % Powder SprayPSN2
705934tolnaftate 0.01 MG/MG Powder SpraySCD2
705934tolnaftate 1 % Powder SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11523-0136-1LotriminDaily Prevent Deodorant160 g in 1 CANAEROSOL, POWDER1602

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11523-013611523-0136-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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 Prevent DeodorantTOLNAFTATEBayer HealthCare LLC.1bb961cd-b6e6-3aff-e063-6394a90a432e2025-12-04WarningsExact identifier
ndc (package): 11523-0136-1
ndc (product): 11523-0136
ndc11 (package): 11523013601
spl id: 4526e2eb-ee88-3ac4-e063-6394a90a133f
spl set id: 1bb961cd-b6e6-3aff-e063-6394a90a432e

Reported adverse events (FAERS/openFDA)#

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