Miconazole Foot Powder

Manufacturer: Davion, Inc.
Effective date: 2022-12-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 21:44:35

Label at a glance#

ProductMiconazole Foot Powder

Active ingredientMICONAZOLE NITRATE

Label structure9 sections

Indications and uses

for the cure of most athlete's foot, jock itch and ringworm

Dosage and administration

Apply as needed

Contacts and useful links#

PhoneLabel contact1-866-964-0939

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Miconazole nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

for the cure of most athlete's foot, jock itch and ringworm

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens
symptoms last more than 7 days or clear up and occur again within a few days

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

Apply as needed

Other information

OTHER SAFETY INFORMATION

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Allantoin, Chloroxylenol, Imidurea, Microcrystalline Cellulose, Tricalcium Phosphate,

Zea Mays Corn Starch

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Pincipal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bulk

Miconazorb Foot Powder Cornstarch

2.5 oz

Products#

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

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

Miconazole Foot Powder
Miconazole
CELLULOSE, MICROCRYSTALLINE
IMIDUREA
TRICALCIUM PHOSPHATE
ZEA MAYS SUBSP. MAYS WHOLE
ALLANTOIN
MICONAZOLE NITRATE
CHLOROXYLENOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
42669-073	42669-073-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
CELLULOSE, MICROCRYSTALLINE	OP1R32D61U	IACT
IMIDUREA	M629807ATL	IACT
TRICALCIUM PHOSPHATE	K4C08XP666	IACT
ZEA MAYS SUBSP. MAYS WHOLE	1G5HNE09V8	IACT
ALLANTOIN	344S277G0Z	IACT
MICONAZOLE NITRATE	VW4H1CYW1K	ACTIB
CHLOROXYLENOL	0F32U78V2Q	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0e004ff4-6c2f-dac6-e063-6394a90a67f9			efbd36cc-3b46-1bc5-e053-2a95a90a3bbd	2024-01-02	Warnings	Exact identifier spl set id: efbd36cc-3b46-1bc5-e053-2a95a90a3bbd

Reported adverse events (FAERS/openFDA)#

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