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Quinsana Anti-Fungal Powder 2 Miconazole Nitrate

Manufacturer
Profoot Inc.
Effective date
2023-11-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:21:14

Label at a glance#

ProductQuinsana Anti-Fungal Powder 2 Miconazole Nitrate
Active ingredientMICONAZOLE NITRATE
Label structure6 sections

Indications and uses

Cures most athlete’s foot and ringworm Effectively relieves itching, cracking, and burning

Dosage and administration

Wash affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night).  Supervise children in the use of this product.  For athlete’s foot: pay special attention to spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.  Use daily for 4 weeks; if condition persists longer, ask a doctor.  This product is not...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconazole Nitrate, 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • Cures most athlete’s foot and ringworm
  • Effectively relieves itching, cracking, and burning

Warnings

WARNINGS SECTION

  • For external use only

Ask a doctor before use

OTC - ASK DOCTOR SECTION

  • on children under 2 years of age

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs 
  • there is no improvement within 4 weeks

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.
  • Apply a thin layer of the product over affected area twice daily (morning and night). 
  • Supervise children in the use of this product. 
  • For athlete’s foot: pay special attention to spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. 
  • Use daily for 4 weeks; if condition persists longer, ask a doctor. 
  • This product is not effective on the scalp or nails.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Zea Mays (Corn) Starch, Tricalcium Phosphate, Microcrystalline Cellulose, Allantoin, Imidazolidinyl Urea, Chloroxylenol, Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

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
29784-14529784-145-85

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
NameUNIIKind
STARCH, CORNO8232NY3SJIACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
ALLANTOIN344S277G0ZIACT
IMIDUREAM629807ATLIACT
CHLOROXYLENOL0F32U78V2QIACT
MICONAZOLE NITRATEVW4H1CYW1KACTIB

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
09bd9ee6-c422-c415-e063-6394a90ac616274b427f-a2c0-4967-a3bf-07ff07eecc802023-11-09WarningsExact identifier
spl id: 09bd9ee6-c422-c415-e063-6394a90ac616
spl set id: 274b427f-a2c0-4967-a3bf-07ff07eecc80

Reported adverse events (FAERS/openFDA)#

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