FDA.reportPublic FDA data

Publix Athletic Foot

Manufacturer
PUBLIX SUPER MARKETS, INC. | Sheffield Pharmaceuticals LLC
Effective date
2024-06-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:15:14

Label at a glance#

ProductPublix Athletic Foot
Active ingredientCLOTRIMAZOLE
Label structure9 sections

Indications and uses

Cures most athlete's foot, jock itch and ringworm Relieves the itching, burning, scaling, chafing and discomfort associated with these conditions

Dosage and administration

Wash the affected area and dry thoroughly. Apply a thin layer of this product over affected area twice daily (morning and night) Supervise children in the use of this product. use daily for 2 weeks. If conditions persist longer, consult a doctor. This product is not effective on the scalp or nails.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Clotrimazole 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • Cures most athlete's foot, jock itch and ringworm
  • Relieves the itching, burning, scaling, chafing and discomfort associated with these conditions

WarningsFor external use only

WARNINGS SECTION

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

When using this product avoid contact with eyes.

Stop use and consult a doctor if

  • irritation occurs
  • if there is not improvement within 2 weeks

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wash the affected area and dry thoroughly.
  • Apply a thin layer of this product over affected area twice daily (morning and night)
  • Supervise children in the use of this product.
  • use daily for 2 weeks.
  • If conditions persist longer, consult a doctor.
  • This product is not effective on the scalp or nails.

Other information 

OTHER SAFETY INFORMATION

  • Store at controlled room temperature 20°-25°C (68°-77°F).
  • Close cap tightly after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Benzyl Alcohol, Cetearyl Alcohol, Cetyl Esters, Octyldodecanol, Polysorbate 60, Sorbitan Monostearate, Tocopheryl Acetate, Water (purified).

Principal Display panel 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Publix Athletes Foot Cream      NDC#  56062-817-28

1% Clotrimazole Cream

 Cures Most athlete's foot

NET WT 1 OZ (28g)

Publix Athlete's Foot 1 oz CartonPublix Athlete's Foot 1 oz Carton

Publix Athlete's Foot 1 oz TubePublix Athlete's Foot 1 oz Tube

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
309367clotrimazole 1 % Topical CreamPSN2
309367clotrimazole 10 MG/ML Topical CreamSCD2
309367clotrimazole 1 % Topical CreamSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CLOTRIMAZOLE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b64d2752-34ef-378a-1f4f-8bff32b0d1aeProduct name420250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9Product name220250121
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6Product name220151106
f5395dd2-4395-d8c6-3477-8c2d4a2f951cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56062-814-282026-01-29C16284748780-149896155-afd3-586f-e063-e6dba90add907e1a25b2-8414-450d-b9da-e624a1feda05

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56062-814-28Publix Athletic Foot28 g in 1 TUBECREAM282
56062-814-28Publix Athletic Foot1 in 1 CARTONCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56062-814PUBLIX ATHLETIC FOOT (CLOTRIMAZOLE 1%) CREAM [PUBLIX SUPER MARKETS, INC.]22 package rows20240715_7e1a25b2-8414-450d-b9da-e624a1feda05.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56062-81456062-814-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
CLOTRIMAZOLEG07GZ97H65ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
BENZYL ALCOHOLLKG8494WBHIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETYL ESTERS WAXD072FFP9GUIACT
OCTYLDODECANOL461N1O614YIACT
POLYSORBATE 60CAL22UVI4MIACT
SORBITAN MONOSTEARATENVZ4I0H58XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT

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
9c2ec1aa-6907-46ed-8e06-ef6ff8cf74417e1a25b2-8414-450d-b9da-e624a1feda052024-06-17WarningsExact identifier
spl id: 9c2ec1aa-6907-46ed-8e06-ef6ff8cf7441
spl set id: 7e1a25b2-8414-450d-b9da-e624a1feda05

Reported adverse events (FAERS/openFDA)#

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