Fungus Master Antifungal Treatment

Manufacturer
Ebanel Laboratories, Inc | Clinical Resolution Laboratory, Inc.
Effective date
2026-02-09
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:37:48

Label at a glance#

ProductFungus Master Antifungal Treatment
Active ingredientMICONAZOLE NITRATE
Label structure7 sections

Indications and uses

Proven clinically effective in the treatment of most athlete’s foot(Tinea Pedis), jock itch(Tinea Cruris) and ringworm(Tinea Corporis). For effective relief of itching, scaling, cracking, burning, redness, Soreness, irritation, discomfort, itchy, scaly skin between the toes, and chafing associated with jock itch.

Dosage and administration

Wash the affected area and dry thoroughly. Apply 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 the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. For athlete’s foot and ringworm use daily for 4 weeks; for ...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconazole Nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • Proven clinically effective in the treatment of most athlete’s foot(Tinea Pedis), jock itch(Tinea Cruris) and ringworm(Tinea Corporis).
  • For effective relief of itching, scaling, cracking, burning, redness, Soreness, irritation, discomfort, itchy, scaly skin between the toes, and chafing associated with jock itch.

Warnings

WARNINGS SECTION

  • Do not use on children under 2 years of age.
  • For external use only.
  • Avoid contact with the eyes.
  • If irritation occurs or if there is no improvement within 4 weeks (for athlete’s foot and ringworm) or within 2 weeks (for jock itch), discontinue use and consult a doctor.

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 the affected area and dry thoroughly. Apply 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 the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. For athlete’s foot and ringworm use daily for 4 weeks; for jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor. This product is not effective on the scalp or nails. Store at 15-30°C (59-86°F)

Other Information

SPL UNCLASSIFIED SECTION

Functional ingredients used in this formula have been shown to improve the appearance of thickened, discolored, and unhealthylooking feet caused by dermatophytic fungi. Urea has been shown to thin, soften, and act as penetrating agent on skin. Undecylenic acid is effective as an emulsifier, cleanser, and preservative.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Arginine, Ascorbyl Palmitate, Carthamus Tinctorius (Safflower) Seed Oil, Cetearyl Alcohol, Cinnamomum Zeylanicum Leaf Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Cocos Nucifera (Coconut) Oil, Cymbopogon Flexuosus Oil, Dimethyl Isosorbide, Dodecane, Eucalyptus Globulus Leaf Oil, Eugenia Caryophyllus (Clove) Flower Oil, Glycerin, Lavandula Angustifolia (Lavender) Flower Oil, Leptospermum Scoparium Branch/Leaf Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Mentha Piperita (Peppermint) Oil, Oreganum Vulgare Leaf Oil, Panthenol, PEG-12 Dimethicone, PEG-40 Hydrogenated Castor Oil, PEG-8 Dilaurate, Persea Gratissima (Avocado) Oil, Phenoxyethanol, Phospholipids, Polysorbate 20, Polysorbate 60, PPG-26-Buteth-26, Punica Granatum Seed Extract, Retinyl Palmitate, Salicylic Acid, Santalum Spicatum Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Benzoate, Sodium Bicarbonate,Tocopheryl Acetate,Undecylenic Acid, Inact ive Ingredients Urea, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

112233

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998521miconazole nitrate 2 % Topical LotionPSN6
998521miconazole nitrate 20 MG/ML Topical LotionSCD6
998521miconazole nitrate 2 % Topical LotionSY6

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508
3a55f4fb-5aec-4c88-0ff7-4d608ad4866aProduct name120140508
5b9a7965-36d2-8412-dcaf-f76a65411611Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72654-001-012026-01-29C16284748780-149896155-caae-586f-e063-e6dba90add90Fungus Master Antifungal Treatment
72654-001-022026-01-29C16284748780-149896155-caae-586f-e063-e6dba90add90Fungus Master Antifungal Treatment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72654-001-01Fungus Master Antifungal Treatment30 mL in 1 BOTTLE, WITH APPLICATORLOTION306
72654-001-02Fungus Master Antifungal Treatment59 mL in 1 BOTTLE, WITH APPLICATORLOTION596

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72654-00172654-001-01, 72654-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 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
Fungus Master Antifungal TreatmentMICONAZOLE NITRATEEbanel Laboratories, Incf7b011b2-11e5-46f1-afed-89f438985e002026-02-09WarningsExact identifier
ndc (package): 72654-001-02
ndc (package): 72654-001-01
ndc (product): 72654-001
ndc11 (package): 72654000102
ndc11 (package): 72654000101
spl id: 4a6d1ee4-a8ad-861a-e063-6294a90a3423
spl set id: f7b011b2-11e5-46f1-afed-89f438985e00

Reported adverse events (FAERS/openFDA)#

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