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(oks i KON a zole)

Index Terms

  • Oxiconazole Nitrate

Dosage Forms

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Cream, External:

Oxistat: 1% (30 g, 60 g, 90 g) [contains benzoic acid, cetyl alcohol, propylene glycol]

Generic: 1% (30 g, 60 g, 90 g)

Lotion, External:

Oxistat: 1% (30 mL, 60 mL) [contains benzoic acid, cetyl alcohol, propylene glycol]

Brand Names: U.S.

  • Oxistat

Pharmacologic Category

  • Antifungal Agent, Imidazole Derivative
  • Antifungal Agent, Topical


The cytoplasmic membrane integrity of fungi is destroyed by oxiconazole which exerts a fungicidal activity through inhibition of ergosterol synthesis. Effective for treatment of tinea pedis, tinea cruris, tinea corporis, and tinea versicolor. Active against Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton violaceum, Microsporum canis, Microsporum audouinii, Microsporum gypseum, Epidermophyton floccosum, Candida albicans, and Malassezia furfur.


In each layer of the dermis; very little systemically after one topical dose


To each layer of the dermis


Urine (<0.3%)

Use: Labeled Indications

Cream: Treatment of tinea pedis (athlete's foot), tinea cruris (jock itch), tinea corporis (ringworm), and tinea (pityriasis) versicolor

Lotion: Treatment of tinea pedis (athlete's foot), tinea cruris (jock itch), tinea corporis (ringworm)


Hypersensitivity to oxiconazole or any component of the formulation

Dosing: Adult

Tinea corporis/tinea cruris: Topical: Cream, lotion: Apply to affected areas 1-2 times daily for 2 weeks

Tinea pedis: Topical: Cream, lotion: Apply to affected areas 1-2 times daily for 1 month

Tinea versicolor: Topical: Cream: Apply to affected areas once daily for 2 weeks

Dosing: Geriatric

Refer to adult dosing.

Dosing: Pediatric

Tinea corporis, tinea cruris, tinea pedis, tinea versicolor: Children ≥12 years and Adolescents: Topical: Cream, lotion: Refer to adult dosing.


For external use only. Avoid occlusive dressings. Wash hands before and after use.


Store between 15°C to 30°C (59°F to 86°F). Shake lotion well before use.

Drug Interactions

There are no known significant interactions.

Adverse Reactions

1% to 10%:

Dermatologic: Pruritus (<2%)

Local: Burning (≤1%)

<1% (Limited to important or life-threatening): Allergic contact dermatitis, dyshidrotic eczema, erythema, fissure, folliculitis, irritation, maceration, nodules, pain, papules, rash, scaling, stinging, tingling


Concerns related to adverse effects:

• Irritation: Discontinue if sensitivity or irritation occurs

Other warnings/precautions:

• Appropriate use: For topical use only; not for ophthalmologic, oral, or vaginal use.

Pregnancy Risk Factor


Pregnancy Considerations

When administered orally, teratogenic effects were not observed in animal reproduction studies.

Patient Education

• Discuss specific use of drug and side effects with patient as it relates to treatment. (HCAHPS: During this hospital stay, were you given any medicine that you had not taken before? Before giving you any new medicine, how often did hospital staff tell you what the medicine was for? How often did hospital staff describe possible side effects in a way you could understand?)

• Patient may experience itching or burning. Have patient report immediately to prescriber severe skin irritation, blistering, edema, oozing, or bleeding (HCAHPS).

• Educate patient about signs of a significant reaction (eg, wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat). Note: This is not a comprehensive list of all side effects. Patient should consult prescriber for additional questions.

Intended Use and Disclaimer: Should not be printed and given to patients. This information is intended to serve as a concise initial reference for healthcare professionals to use when discussing medications with a patient. You must ultimately rely on your own discretion, experience, and judgment in diagnosing, treating, and advising patients.