FDA.reportPublic FDA data

Walgreens Athlete's Foot Powder Spray

Manufacturer
Walgreens Company
Effective date
2026-09-23
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
daily-update
Hydrated at
2026-09-25 02:01:17

Label at a glance#

ProductMiconazole Nitrate
Active ingredientMICONAZOLE NITRATE
Label structure9 sections

Indications and uses

cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris) relieves symtoms of athlete's foot, including itching, burning and cracking

Dosage and administration

wash affected area and dry thoroughly shake can well and spray a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor supervise children in the use of this product for athlete's foot: pay special attention to spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily use daily for 4 weeks for athlete's foot and ringwor...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconozole nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris)
  • relieves symtoms of athlete's foot, including itching, burning and cracking

Warnings

WARNINGS SECTION

For external use only.

Extremely Flammable:

SPL UNCLASSIFIED SECTION

Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120 o F. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

Do not use

OTC - DO NOT USE SECTION

on children under 2 years of age unless directed by a doctor.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes or mouth
  • use only as directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs
  • no improvement within 4 weeks for athlete's foot and ringworm; 2 weeks for jock itch

Keep out of 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 affected area and dry thoroughly
  • shake can well and spray a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
  • supervise children in the use of this product
  • for athlete's foot: pay special attention to spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
  • use daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks for jock itch; if condition persists, consult a doctor
  • this product is not effective on the scalp or nails

Other infomation

OTHER SAFETY INFORMATION

  • Store between 20 o and 30 o C (68 o and 86 o F)
  • if nozzle clogs, clean with a pin

Inactive ingredients

INACTIVE INGREDIENT SECTION

ISOBUTANE, SD ALCOHOL 40-B, KAOLIN, ZEA MAYS (CORN) STARCH, DISTEARDIMONIUM HECTORITE

Questions

OTC - QUESTIONS SECTION

Call 1-866-964-0939

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens
free+pure

Athlete's
Foot
Powder
Spray
Miconazole nitrate 2%, Antifungal

Compare to the active ingredient in
Lotrimin AF

Medicated | Antifungal | Talc-free

Relieves itching, cracking & burning

Cures most athlete's foot

Comforts & refreshes

Free + Pure is:
. Fragrance free
. Hypoallergenic
. Paraben free

NET WT. 4.6 OZ. (130 g)

cartoncarton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130311917063294GTIN-13: 0311917063294
EAN-13: 0311917063294
GTIN-12: 311917063294
UPC-A: 311917063294
GTIN storage (14 digits): 00311917063294		Walgreens_Athletes Foot Miconazole Powder Spray_Aluminum Litho 46-MPSTWG-02.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3a55f4fb-5aec-4c88-0ff7-4d608ad4866aProduct name120140508
5b9a7965-36d2-8412-dcaf-f76a65411611Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-74180363-7418-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
MICONAZOLE NITRATEVW4H1CYW1KACTIB
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
KAOLIN24H4NWX5COIACT
ISOBUTANEBXR49TP611IACT
STARCH, CORNO8232NY3SJIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
102026-06-22monthly-update2026-07-17 21:35:07
92026-06-04daily-update2026-06-11 05:10:31
82025-12-05full-release2026-06-01 01:21:27
62025-11-06monthly-update2026-06-03 17:39:33
52024-11-20full-release2026-06-01 00:38:30

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
54bb706f-ad0e-de9b-e063-6394a90a7a1ece564e4d-429f-60a9-e053-2a95a90ae4fe2026-06-22WarningsExact identifier
spl set id: ce564e4d-429f-60a9-e053-2a95a90ae4fe

Reported adverse events (FAERS/openFDA)#

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